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Harjinder Singh
Dept. Of Botany
Meerut College, Meerut
1H. SINGH
Faculty: Science
Department: Botany
Name: Harjinder Singh
Name of degree programme: B Sc. II
Course: Cytology, Genetics, Evolution and Ecology
2H. SINGH
 Plasma membrane or cell membrane is an outermost
envelope surrounding the cytoplasm of cell, that
separates and protect the cell contents from the
extracellular environment and provides the
connectivity between the cell and it’s external
environment.
 It is living and selective permeable membrane
common to all cells made of phospholipids, proteins
and some conjugated molecules. It regulates the
materials that enter and exit the cell.
 Cell Membrane can be divide into:
 a) Cytoplsamic membrane: It controls the internal
environment of the cell.
 b) Internal membrane: It encloses some cell
organelles –mitochondria, chloroplast, nucleus etc.
3H. SINGH
 First time In 1672, Nehemiah Grew studying the cell made the description of “mass of
bubbles” in relation to plant parenchyma . In 1682 he reported that the cell membrane
resembled a lace-like material. His research established the fact that both plant cavities
and their fibers showed continuity and all plant organisms had membrane systems.
• In 1837,Schleiden (botanist) and in 1839, Schwann suggested that there was universal
mechanism for the development of cell.
• In 1844 C. Nageli conducted the membrane permeability studies.
• In 1854 N. Pringsheim showed that there was a membrane around protoplast of which
permeability varied depend on conditions.
• In 1855, C. Nageli and K. Cramer further conducted membrane permeability tests of plant
cells and established the existence of cell membrane around protoplasm.
• In 1877 Wilhelm Pfeffer proposed the Cell Membrane Theory that cell was seen to be
enclosed by a thin surface.
• In 1899 C. Overton showed that membrane was a lipid structure.
• In 1925 Gorter and Grandel studied the RBCs that suggested that membrane was
consisted of lipids only ( Idea rejected).
• 1n 1932 Harvey and Cole first suggested that lipid membrane was surrounded by proteins.
• !n 1935 Daneilli and Davson proposed first classical (Sandwich) model.
• In 1959 Robetson proposed famous Unit Membrane Concept( Trilaminar Model)
, with the help of electron microscope and showed tht plasma membrane consists of three
layers: outer and inner of proteins and middle of lipids.
• In 1972 Singer and Nicholson proposed most accepted Fluid Mosaic Model describing
that plasma membrane are composed of phospholipids bilyer with various protein
molecules floating within it.
4H. SINGH
 Chemically plasma membrane consists of lipids,
proteins held together by non covalent bonds and
some carbohydrates are also attached to the lipids
and proteins
 The ratio of lipid to protein in a membrane varies,
depending on the type of cellular membrane
(endoplasmic reticulum vs. Golgi apparatus), the
type of organism (bacterium vs. plant vs. animal),
and the type of cell.
 Various kinds of enzymes are reported in different
biomembranes e.g. phosphatases, ATP-ase,
esterases, nucleases etc.
5H. SINGH
 Depending upon it’s characteristic lipid composition, each type of cellular
membrane (3-6 nm thick) differs from one another in the types of lipids, the
nature of the head groups, and the particular species of fatty acyl chain.
 Membranes contain a wide diversity of lipids, all of which are amphipathic; that
is, they contain both hydrophilic and hydrophobic regions. There are three
main types of membrane lipids: phosphoglycerides, sphingolipids, and
cholesterol (in animals) and sterol (plants).
 The phospholipid bilayer has a polar hydrophilic (water attracting) head of
phospholipids facing outwards and their non-polar, hydrophobic (water
repelling) tails facing in towards the middle of the bilayer. membrane
phosphoglycerides have an additional group linked to the phosphate, most
commonly either choline (forming phosphatidylcholine, PC), ethanolamine
(forming phosphatidylethanolamine, PE), serine (forming phosphatidylserine,
PS), or inositol (forming phosphatidylinositol, PI). Each of these groups is small
and hydrophilic and, together with the negatively charged phosphate to which it
is attached, forms a highly water-soluble domain at one end of the molecule,
called the head group. The fatty acyl chains are hydrophobic, unbranched
hydrocarbons approximately 16 to 22 carbons in length.
 Hydrophilic portions of both proteins and phospholipids are maximally exposed
to water resulting in a stable membrane structure.
6H. SINGH
The structure of a phospholipid molecule: This phospholipid molecule
is composed of a hydrophilic head and two hydrophobic tails. The
hydrophilic head group consists of a phosphate-containing group attached
to a glycerol molecule. The hydrophobic tails, each containing either a
saturated or an unsaturated fatty acid, are long hydrocarbon chains.
7H. SINGH
8H. SINGH
 The back bone of the membrane is composed of amphiphilic phospholipid molecules.
The hydrophilic or water-loving areas of these molecules are in contact with the aqueous
fluid both extracellular and cytoplsamic sides the cell. Hydrophobic, or water-repelling
molecules, tend to be non- polar.
 A phospholipid molecule consists of a three-carbon glycerol backbone with two fatty acid
molecules attached to carbons 1 and 2, and a phosphate-containing group attached to the
third carbon. This arrangement gives the overall molecule, a polar with negative charge,
and a tail (the fatty acids), with no charge.
 They interact with other non-polar molecules in chemical reactions, but generally do not
interact with polar molecules. When placed in water, hydrophobic molecules tend to form
a ball or cluster. The hydrophilic regions of the phospholipids tend to form hydrogen
bonds with water and other polar molecules on both the exterior and interior of the cell.
 Thus, the membrane surfaces that face the interior and exterior of the cell are hydrophilic.
In contrast, the middle of the cell membrane is hydrophobic and will not interact with
water. Therefore, phospholipids form an excellent lipid bilayer cell membrane that
separates fluid within the cell from the fluid outside of the cell.
❖ Lipid bilayer facilitates the regulated fusion or budding of membranes and has ability to
self-assemble. It is important for maintaining the proper internal composition of a cell, in
separating electric charges across the plasma membrane, and in many other cellular
activities.
9H. SINGH
 It is the membrane Proteins, that are
responsible for carrying out specific cell
membrane functions. Depending on the cell
type and the particular organelle within that cell,
a membrane may contain hundreds of different
proteins.
 Each membrane protein has a defined
orientation relative to the cytoplasm, so that the
properties of one surface of a membrane are
very different from those of the other
surface(Sidedness)
continue……
10H. SINGH
 On the basis of their relationship(position) to the lipid bilayer
membrane proteins can be grouped into three distinct classes,
though they perform various functions.
 1. Integral proteins or transmembrane proteins : They present
across the lipid bilayer thus have domains that protrude from both
the extracellular and cytoplsamic sides of the membrane.
 2. Peripheral proteins : They are located entirely outside of the lipid
bilayer, on either the cytoplsamic or extracellular side, yet are
associated with the surface of the membrane by non covalent bonds.
 3. Lipid-anchored proteins: They are located outside the lipid
bilayer, on either the extracellular or cytoplsamic surface, but are
covalently linked to a lipid molecule that is situated within the bilayer.
11H. SINGH
1. Integral proteins : They are amphipathic in nature
may act as
a) receptors that bind specific substances at the membrane
surface.
b) channels or transporters involved in the movement of ions
and solutes across the membrane.
c) agents that transfer electrons during the processes of
photosynthesis and respiration.
Integral or transmembrane contain one or more transmembrane
helices.
12H. SINGH
• Integral proteins are embedded permanently in the
membrane by hydrophobic, electrostatic, and other non-covalent
interaction. The most common type of integral proteins are
transmembrane proteins, which span across the lipid bilayer.
• They usually adopt an α-helical configuration . Single-pass
membrane proteins cross the membrane only once, while the
multiple-pass membrane proteins are crossing the membrane
several times.
• Many of the integral membrane proteins function as ion channels
or transporters, regulating the influx of ions/molecules between the
extracellular and intracellular spaces.
• Cell surface receptors, linkers, enzymatic proteins, and proteins
responsible for cell adhesion are all classes of integral membrane
proteins .
• Recent studies have shown that activity of these proteins
depends on the lipid composition and membrane-protein
interactions.
13H. SINGH
2. Peripheral proteins : They are associated
with the membrane by weak electrostatic bonds .
These proteins provide mechanical support for the
membrane and function as an anchor for integral
membrane proteins. Some peripheral proteins on the
internal plasma membrane surface function as
enzymes, specialized coats or factors that transmit
transmembrane signals. They have a dynamic
relationship with the lipid membrane
14H. SINGH
❖ Peripheral proteins temporarily bind to the surface of the
membrane with weak interactions. They have a unique amino acid
sequence which allows them to bind and congregate on the surface
of the membrane.
• There is no hydrophobic region of amino acids in peripheral
proteins structure, therefore they can attach to membrane surface
without being locked onto it.
•The primary role of peripheral proteins is to provide a point of
attachment for other components to the cell membrane. Both
membrane cytoskeleton and components of extracellular matrix are
linked to the cell membrane through peripheral proteins, thus they
help the cell to maintain its
shape while the membrane remains flexible to bend based on the
cellular functions.
• They are also involved in various other functions including cell
communication, energy transduction, and molecule
transfer across the membrane
15H. SINGH
3.Lipid-Anchored Membrane Proteins : Various
types of lipid-anchored membrane proteins present on the external
face of the plasma membrane . They are bound to the membrane by a
small, complex oligosaccharide linked to a molecule of
phosphatidylinositol and called GPI (glycosyl-phosphatidylinositol )-
anchored proteins.They may be also present on the inner side of
membrane and anchored to the lipids by hydrocarbon chains
They act as receptors, enzymes, and cell-adhesion proteins.
16H. SINGH
 The plasma membranes of eukaryotic cells also contain
carbohydrates in the form of conjugated molecules.
 Depending on the species and cell type, the carbohydrate content of
the plasma membrane ranges between 2 and 10 percent.
 More than 90 percent of the membrane’s carbohydrate is covalently
linked to proteins to form glycoproteins and remaining
carbohydrate is covalently linked to lipids to form glycolipids.
 Glycoproteins are almost found in all living organisms and serve a
number of important roles as structural molecules, immunologic
molecules, transport molecules, receptors, enzymes, and hormones.
 Along with carbohydrates some molecules of
cholesterol(Animal)/ Sterol(Plant) are also embedded in the lipid
bilayer to provide fluidity to the membrane.
17H. SINGH
18H. SINGH
19H. SINGH
 1.Gorter and Grendel model (1925)
 2.Bilayer Model or Classical Sandwich Model
by Danielli and Davson(1935)
 3. Unit Membrane Concept (Trilaminar Model)
by J D Robertson(1959)
 4.Fluid Mosaic Model by J Singer and G
Nicolson(1972)
20H. SINGH
 They studied on RBCs. of various mammals and
proposed that cell membrane is composed of
lipids only.
 Hydrophobic ends toward the interior and
hydrophilic ends point outward of the membrane.
 They showed that molecules could make single
or double layers.
 They opened the door to the identification of the
molecular structures of the membrane
 Though model was imperfect because lipids are
impermeable to the molecules.
21H. SINGH
 After the findings of Harvey and
Cole that lipids layer are
surrounded by proteins, Danielli
and Davson came up with a
sandwich membrane model or
protein--protein model.
 According to this model, there are
four layers as P-L-L-P.
The surfaces were surrounded by
a thin layer of protein on both
sides just like sandwich..
 Lipids molecule are amphipathic
with hydrophilic heads towards
protein and hydrophobic tails
towards centre.
 But due to lack of the facility of
higher resolution power of
electron microscope the actual
assembly of protein and lipids
could not revealed.
---2nm
--3.5nm
--2nm
22H. SINGH
 The amount and types of vary greatly
between different cells.
 It was unable to describe how the proteins
would allow the membrane to change shape
without bonds being broken.
 Membrane proteins are largely hydrophobic
and therefore should not be found where the
model positioned them.
23H. SINGH
 In 1959, Robertson ,observed the structure in
electron micrograph staining the tissues with
osmium and saw Trilaminar appearance of
membranes.
 He saw no space for the pores in the micrograph.
Osmium binds preferentially to the polar head
groups of the lipid bilayer, producing the
trilaminar.
 The transverse sections of the membranes
revealed the three-layer membrane structure
known as the ‘railway’. In this view, which would
later be called “Unit membrane”, there was a
third layer between the two dense layers which
was less dense pattern.
 Robertson suggested that the dark regions were
protein layers, while the open area in the middle
was equivalent to the lipid layer
 Though this model provided great insight into the
structure of PM but functioning could not
understand perfectly.
 In 1964, Brady and Trams reported that
membrane are composed of lipids and proteins,
where proteins entered the membrane and the
lipid components are fluid, that paved the way to
development of Fluid Mosaic Model 24H. SINGH
 With the development of freeze-breaking techniques
and immuno-electron microscopy techniques, scientists
identified isolated membrane proteins and membrane-
embedded proteins through antibodies.
 On the basis of their findings Singer and Nicolson introduced most
accepted and famous FLUID MOSAIC MEMBRANE MODEL in
1972.
“This model describe P M as a flexible boundary of
the cell. It states that it is a lipid bilayer in which
proteins occur as a ‘mosaic’ of discontinuous
particles that penetrate irregularly deep or even
through the lipid bilayer. Phospholipids molecules
present in a fluid state and capable to move and
rotate freely”.
25H. SINGH
26H. SINGH
 According to this model,
 It is ‘ fluid’ because phospholipid
are free to move. Phospholipids in
the lipid bilayer can either move
rotationally, laterally in one bilayer, or
occasionally undergo
transverse movement (flip flop)
between bilayers They can only move
from side to side, however, not
through the membrane.
▪ It is called a ‘ mosaic’ because the
proteins are embedded in the
phospholipid bilayer (like mosaic
tiles embedded in mortar).
 Hydrophilic portions of both proteins
and phospholipids are maximally
exposed to water resulting in a stable
membrane structure.
H. SINGH
28H. SINGH
Transport:
The plasma membrane regulates physically
transporting substances from one side of the
membrane to another, often from a region where
the solute is at low concentration into a region of
much higher concentration.
It allows a cell to accumulate substances for
metabolism and building macromolecules.
A protein that spans the membrane may provide a
hydrophilic channel ( aquaporins) across the
membrane that is selective for a particular solute
or porins for selected molecules.
-
29H. SINGH
 There are four broad categories of molecules found in the cellular environment. Some
of these molecule can cross the membrane and some of them need the help of other
molecules or processes.
 hydrophilic Molecules are capable of forming bonds with water and other
hydrophilic molecules, called polar molecules.
 hydrophobic are called nonpolar molecules. Here are the 4 types:
 Small, nonpolar molecules (ex: oxygen and carbon dioxide) can pass through the
lipid bilayer and do so by squeezing through the phospholipid bilayers. They don't
need proteins for transport and can diffuse across quickly.
 Small, polar molecules (ex: water): water molecules diffuse through the membrane
without the help of proteins but it slower process because the interior of the
phospholipid bilayer is made up of the hydrophobic tails.
 Large, nonpolar molecules (ex: carbon rings): These rings can pass through but it is
also slow process.
 Large, polar molecules (ex: simple sugar - glucose) and ions: The charge of an ion,
and the size and charge of large polar molecules pass through the nonpolar region of
the phospholipid membrane with the help of transmembrane proteins
30H. SINGH
1. Passive Transport:
a) Simple Diffusion.
b) Facilitated Diffusion
2. Active Transport: It may be -
a) Primary active transport.
b) Secondary Active transport
3. Bulk TRANSPORT:
a) Endocytosis
b) Exocytosis
31H. SINGH
 (A) Passive Diffusion:
Diffusion of nonpolar,
hydrophobic molecules like
Lipids from high to low
concentration gradient /or
 Simple diffusion through
an aqueous channel
(aquaporins)formed within
an integral membrane
protein or a cluster of such
proteins. As in a, movement
is always down a
concentration gradient.
 It does not required energy
or membrane transport
proteins.
 e.g. transport of gases, ions
and lipid soluble molecules
32H. SINGH
▪ Diffusion of molecules down the
concentration gradient which
required carrier proteins but
does not require energy.
▪ Diffusion of hydrophilic
molecules ,in which solute
molecules bind specifically to a
membrane protein carriers
(facilitate transporters).
▪ Based on the direction of
molecules it may be;
▪ a) Uniport: Transport of single
type of molecule in one direction.
▪ B) Antiport: transport of
molecules in opposite direction.
33H. SINGH
 It is diffusion against concentration gradient
from Low to high. Active transport by means
of a protein transporter (protein pumps)
with a specific binding site that undergoes a
change through energy driven by ATP .
 It may be:
a) Primary Active transport: Transport against
gradient in which energy(ATP) used directly.
It requires carriers. e. g. sodium-potassium
pump, calcium pump.
 b) Secondary Active Transport: Transport
against gradient in which energy (ATP) is
used indirectly. Here tow or three molecules
coupled e.g.NA-K and ATPase
34H. SINGH
35H. SINGH
 Also called transport by vesicles formation, which
involves formation of membrane bound vesicles.
 It facilitates transport of macromolecules.
Two Types:
1. Endocytosis : is when a cell ingests relatively larger
contents than the single ions or molecules that
pass through channels. It may be:
a) Phagocytosis: engulfing of solid particles.
b) Pinocytosis: engulfing of liquid particles.
2. Exocytosis : expulsing out of the molecules from the
cell the cell membrane.
The shape of the membrane itself changes to allow
molecules to enter or exit the cell.
36H. SINGH
 Passive osmosis and diffusion: transports
gases (such as O2 and CO2) and other small
molecules and ions
 Transmembrane protein channels and
transporters: transports small organic
molecules such as sugars or amino acids
 Endocytosis: transports large molecules (or
even whole cells) by engulfing them
 Exocytosis: removes or secretes substances
such as hormones or enzymes
37H. SINGH
 Some glycoprotein serve
as identification tags that
are specifically recognized
by other cells.
 Cells are able to recognize
other through these tags.
 Provide mechanisms for a
cell to recognize itself and
other cells of its particular
individual organisms vs.
non-self (foreign
materials).
38H. SINGH
 Membrane proteins of adjacent cell may
be hooked together in various kinds of
junction:
 Plasmodesmata are junctions between plant
cells, whereas animal cell contacts are carried
out through tight junctions, gap junctions, and
desmosomes.
 A plasmodesma is a channel between the cell
walls of two adjacent plant cells that allow
materials to pass from the cytoplasm of one
plant cell to the cytoplasm of an adjacent cell.
 A tight junction is a watertight seal between
two adjacent animal cells, which prevents
materials from leaking out of cells.
 Desmosomes connect adjacent cells when
cadherins in the plasma membrane connect to
intermediate filaments.
 Gap junction (communicating junction),
provide cytoplsamic channel for ions,
nutrients and other substances that allow the
cells to communicate.
39H. SINGH
 Enzymatic activity
▪ Several enzymes in a membrane are ordered
as a team that carries out sequential steps in
metabolic pathway.
 Signal transduction
 The plasma membrane plays a critical role in
the response of a cell to external stimuli such
as a hormone, a process known as signal
transduction.
 Membranes possess receptor proteins that
combine with specific molecules (ligands) or
respond to other types of stimuli such as light
or mechanical tension.
40H. SINGH
 Microfilaments or other elements of the cytoskeleton
may bonded to membrane proteins, a function that
helps maintain cell shape and fixes the location
of certain membrane proteins .
 Protein that adhere to the ECM can coordinate
extracellular and intracellular changes. (integrate
changes occurring outside and inside the cell)
Fibres of
extracellular matrix
(ECM)
41H. SINGH
 Plasma Membranes are intimately involved in the
processes by which one type of energy is converted
to another type (energy transduction).
 The most fundamental energy transduction occurs
during photosynthesis when energy in sunlight is
absorbed by membrane-bound pigments, converted
into chemical energy, and stored in carbohydrates.
 Membranes are also involved in the transfer of
chemical energy from carbohydrates and fats to ATP.
In eukaryotes, the machinery for these energy
conversions is contained within membranes of
chloroplasts and mitochondria.
42H. SINGH
 The structure of Phospholipid responsible for the
basic function of membranes as barriers between
two aqueous compartments. Because the interior of
the phospholipid bilayer is occupied by
hydrophobic fatty acid chains, the membrane is
impermeable to water-soluble molecules, including
ions and most biological molecules. This protects all
the components of the cell from the outside
environment and allows separate activities to occur
inside and outside the cell.
 It also provides structural support to the cell. It
tethers the cytoskeleton which is a network of
protein filaments inside the cell that hold all the
parts of the cell in place.
43H. SINGH
 Plasma membranes are selectively permeable (or
semi-permeable), meaning that only certain
molecules can pass through them.
 Water, oxygen, and carbon dioxide can easily
travel through the membrane.
 Generally, ions (e.g. sodium, potassium) and polar
molecules cannot pass through the membrane;
they must go through specific protein channels or
pores in the membrane instead of freely diffusing
through.
 This way, the membrane can control the rate at
which certain molecules can enter and exit the cell.
44H. SINGH
 The plasma membrane may have extensions,
such as whip-like flagella or brush-like cilia, that
give it other functions.
 In single-celled organisms, these membrane
extensions may help the organisms to move.
 In multicellular organisms, the extensions have
different functions.
45H. SINGH
 Plasma Membrane acts as physical barrier b/t extracellular
environment and cytoplasm of the cell.
 Gives the shape to the cell and protects the cell from external
environment.
 It is selectively permeable and hence regulates the transport of
molecules. Lipid soluble molecules like O2 and CO2 and water can
easily diffuse.
 Different kinds of membrane proteins catalyze respective enzymatic
activities
 Participates in absorption, excretion and secretion.
 It is responsible for intercellular communication.
 It helps in maintaining the turgidity of the cell.
 It serves as a receptor for various chemical stimuli such as amino
acids, hormones, and sugars.
 In certain unicellular organisms like amoeba, plasma membrane
performs the function of ingestion of food (endocytosis) and
locomotion too. It also facilitate exocytosis process

46H. SINGH
 Cell membranes are dynamic (not static),
fluid structure which held together by
hydrophobic interactions.
 Membrane fluidity can be affected by:
a)The movement of phospholipids and some
proteins.
b) Phospholipids with unsaturated hydrocarbon
tails maintain membrane fluidity at lower
temperature.
c) Length of fatty acyl chain.
d) Presence of cholesterol/ sterol(plants).
47H. SINGH
48H. SINGH
THANKS…….
49H. SINGH

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Plasma Membrane (Structure and Functions)

  • 1. Harjinder Singh Dept. Of Botany Meerut College, Meerut 1H. SINGH
  • 2. Faculty: Science Department: Botany Name: Harjinder Singh Name of degree programme: B Sc. II Course: Cytology, Genetics, Evolution and Ecology 2H. SINGH
  • 3.  Plasma membrane or cell membrane is an outermost envelope surrounding the cytoplasm of cell, that separates and protect the cell contents from the extracellular environment and provides the connectivity between the cell and it’s external environment.  It is living and selective permeable membrane common to all cells made of phospholipids, proteins and some conjugated molecules. It regulates the materials that enter and exit the cell.  Cell Membrane can be divide into:  a) Cytoplsamic membrane: It controls the internal environment of the cell.  b) Internal membrane: It encloses some cell organelles –mitochondria, chloroplast, nucleus etc. 3H. SINGH
  • 4.  First time In 1672, Nehemiah Grew studying the cell made the description of “mass of bubbles” in relation to plant parenchyma . In 1682 he reported that the cell membrane resembled a lace-like material. His research established the fact that both plant cavities and their fibers showed continuity and all plant organisms had membrane systems. • In 1837,Schleiden (botanist) and in 1839, Schwann suggested that there was universal mechanism for the development of cell. • In 1844 C. Nageli conducted the membrane permeability studies. • In 1854 N. Pringsheim showed that there was a membrane around protoplast of which permeability varied depend on conditions. • In 1855, C. Nageli and K. Cramer further conducted membrane permeability tests of plant cells and established the existence of cell membrane around protoplasm. • In 1877 Wilhelm Pfeffer proposed the Cell Membrane Theory that cell was seen to be enclosed by a thin surface. • In 1899 C. Overton showed that membrane was a lipid structure. • In 1925 Gorter and Grandel studied the RBCs that suggested that membrane was consisted of lipids only ( Idea rejected). • 1n 1932 Harvey and Cole first suggested that lipid membrane was surrounded by proteins. • !n 1935 Daneilli and Davson proposed first classical (Sandwich) model. • In 1959 Robetson proposed famous Unit Membrane Concept( Trilaminar Model) , with the help of electron microscope and showed tht plasma membrane consists of three layers: outer and inner of proteins and middle of lipids. • In 1972 Singer and Nicholson proposed most accepted Fluid Mosaic Model describing that plasma membrane are composed of phospholipids bilyer with various protein molecules floating within it. 4H. SINGH
  • 5.  Chemically plasma membrane consists of lipids, proteins held together by non covalent bonds and some carbohydrates are also attached to the lipids and proteins  The ratio of lipid to protein in a membrane varies, depending on the type of cellular membrane (endoplasmic reticulum vs. Golgi apparatus), the type of organism (bacterium vs. plant vs. animal), and the type of cell.  Various kinds of enzymes are reported in different biomembranes e.g. phosphatases, ATP-ase, esterases, nucleases etc. 5H. SINGH
  • 6.  Depending upon it’s characteristic lipid composition, each type of cellular membrane (3-6 nm thick) differs from one another in the types of lipids, the nature of the head groups, and the particular species of fatty acyl chain.  Membranes contain a wide diversity of lipids, all of which are amphipathic; that is, they contain both hydrophilic and hydrophobic regions. There are three main types of membrane lipids: phosphoglycerides, sphingolipids, and cholesterol (in animals) and sterol (plants).  The phospholipid bilayer has a polar hydrophilic (water attracting) head of phospholipids facing outwards and their non-polar, hydrophobic (water repelling) tails facing in towards the middle of the bilayer. membrane phosphoglycerides have an additional group linked to the phosphate, most commonly either choline (forming phosphatidylcholine, PC), ethanolamine (forming phosphatidylethanolamine, PE), serine (forming phosphatidylserine, PS), or inositol (forming phosphatidylinositol, PI). Each of these groups is small and hydrophilic and, together with the negatively charged phosphate to which it is attached, forms a highly water-soluble domain at one end of the molecule, called the head group. The fatty acyl chains are hydrophobic, unbranched hydrocarbons approximately 16 to 22 carbons in length.  Hydrophilic portions of both proteins and phospholipids are maximally exposed to water resulting in a stable membrane structure. 6H. SINGH
  • 7. The structure of a phospholipid molecule: This phospholipid molecule is composed of a hydrophilic head and two hydrophobic tails. The hydrophilic head group consists of a phosphate-containing group attached to a glycerol molecule. The hydrophobic tails, each containing either a saturated or an unsaturated fatty acid, are long hydrocarbon chains. 7H. SINGH
  • 9.  The back bone of the membrane is composed of amphiphilic phospholipid molecules. The hydrophilic or water-loving areas of these molecules are in contact with the aqueous fluid both extracellular and cytoplsamic sides the cell. Hydrophobic, or water-repelling molecules, tend to be non- polar.  A phospholipid molecule consists of a three-carbon glycerol backbone with two fatty acid molecules attached to carbons 1 and 2, and a phosphate-containing group attached to the third carbon. This arrangement gives the overall molecule, a polar with negative charge, and a tail (the fatty acids), with no charge.  They interact with other non-polar molecules in chemical reactions, but generally do not interact with polar molecules. When placed in water, hydrophobic molecules tend to form a ball or cluster. The hydrophilic regions of the phospholipids tend to form hydrogen bonds with water and other polar molecules on both the exterior and interior of the cell.  Thus, the membrane surfaces that face the interior and exterior of the cell are hydrophilic. In contrast, the middle of the cell membrane is hydrophobic and will not interact with water. Therefore, phospholipids form an excellent lipid bilayer cell membrane that separates fluid within the cell from the fluid outside of the cell. ❖ Lipid bilayer facilitates the regulated fusion or budding of membranes and has ability to self-assemble. It is important for maintaining the proper internal composition of a cell, in separating electric charges across the plasma membrane, and in many other cellular activities. 9H. SINGH
  • 10.  It is the membrane Proteins, that are responsible for carrying out specific cell membrane functions. Depending on the cell type and the particular organelle within that cell, a membrane may contain hundreds of different proteins.  Each membrane protein has a defined orientation relative to the cytoplasm, so that the properties of one surface of a membrane are very different from those of the other surface(Sidedness) continue…… 10H. SINGH
  • 11.  On the basis of their relationship(position) to the lipid bilayer membrane proteins can be grouped into three distinct classes, though they perform various functions.  1. Integral proteins or transmembrane proteins : They present across the lipid bilayer thus have domains that protrude from both the extracellular and cytoplsamic sides of the membrane.  2. Peripheral proteins : They are located entirely outside of the lipid bilayer, on either the cytoplsamic or extracellular side, yet are associated with the surface of the membrane by non covalent bonds.  3. Lipid-anchored proteins: They are located outside the lipid bilayer, on either the extracellular or cytoplsamic surface, but are covalently linked to a lipid molecule that is situated within the bilayer. 11H. SINGH
  • 12. 1. Integral proteins : They are amphipathic in nature may act as a) receptors that bind specific substances at the membrane surface. b) channels or transporters involved in the movement of ions and solutes across the membrane. c) agents that transfer electrons during the processes of photosynthesis and respiration. Integral or transmembrane contain one or more transmembrane helices. 12H. SINGH
  • 13. • Integral proteins are embedded permanently in the membrane by hydrophobic, electrostatic, and other non-covalent interaction. The most common type of integral proteins are transmembrane proteins, which span across the lipid bilayer. • They usually adopt an α-helical configuration . Single-pass membrane proteins cross the membrane only once, while the multiple-pass membrane proteins are crossing the membrane several times. • Many of the integral membrane proteins function as ion channels or transporters, regulating the influx of ions/molecules between the extracellular and intracellular spaces. • Cell surface receptors, linkers, enzymatic proteins, and proteins responsible for cell adhesion are all classes of integral membrane proteins . • Recent studies have shown that activity of these proteins depends on the lipid composition and membrane-protein interactions. 13H. SINGH
  • 14. 2. Peripheral proteins : They are associated with the membrane by weak electrostatic bonds . These proteins provide mechanical support for the membrane and function as an anchor for integral membrane proteins. Some peripheral proteins on the internal plasma membrane surface function as enzymes, specialized coats or factors that transmit transmembrane signals. They have a dynamic relationship with the lipid membrane 14H. SINGH
  • 15. ❖ Peripheral proteins temporarily bind to the surface of the membrane with weak interactions. They have a unique amino acid sequence which allows them to bind and congregate on the surface of the membrane. • There is no hydrophobic region of amino acids in peripheral proteins structure, therefore they can attach to membrane surface without being locked onto it. •The primary role of peripheral proteins is to provide a point of attachment for other components to the cell membrane. Both membrane cytoskeleton and components of extracellular matrix are linked to the cell membrane through peripheral proteins, thus they help the cell to maintain its shape while the membrane remains flexible to bend based on the cellular functions. • They are also involved in various other functions including cell communication, energy transduction, and molecule transfer across the membrane 15H. SINGH
  • 16. 3.Lipid-Anchored Membrane Proteins : Various types of lipid-anchored membrane proteins present on the external face of the plasma membrane . They are bound to the membrane by a small, complex oligosaccharide linked to a molecule of phosphatidylinositol and called GPI (glycosyl-phosphatidylinositol )- anchored proteins.They may be also present on the inner side of membrane and anchored to the lipids by hydrocarbon chains They act as receptors, enzymes, and cell-adhesion proteins. 16H. SINGH
  • 17.  The plasma membranes of eukaryotic cells also contain carbohydrates in the form of conjugated molecules.  Depending on the species and cell type, the carbohydrate content of the plasma membrane ranges between 2 and 10 percent.  More than 90 percent of the membrane’s carbohydrate is covalently linked to proteins to form glycoproteins and remaining carbohydrate is covalently linked to lipids to form glycolipids.  Glycoproteins are almost found in all living organisms and serve a number of important roles as structural molecules, immunologic molecules, transport molecules, receptors, enzymes, and hormones.  Along with carbohydrates some molecules of cholesterol(Animal)/ Sterol(Plant) are also embedded in the lipid bilayer to provide fluidity to the membrane. 17H. SINGH
  • 20.  1.Gorter and Grendel model (1925)  2.Bilayer Model or Classical Sandwich Model by Danielli and Davson(1935)  3. Unit Membrane Concept (Trilaminar Model) by J D Robertson(1959)  4.Fluid Mosaic Model by J Singer and G Nicolson(1972) 20H. SINGH
  • 21.  They studied on RBCs. of various mammals and proposed that cell membrane is composed of lipids only.  Hydrophobic ends toward the interior and hydrophilic ends point outward of the membrane.  They showed that molecules could make single or double layers.  They opened the door to the identification of the molecular structures of the membrane  Though model was imperfect because lipids are impermeable to the molecules. 21H. SINGH
  • 22.  After the findings of Harvey and Cole that lipids layer are surrounded by proteins, Danielli and Davson came up with a sandwich membrane model or protein--protein model.  According to this model, there are four layers as P-L-L-P. The surfaces were surrounded by a thin layer of protein on both sides just like sandwich..  Lipids molecule are amphipathic with hydrophilic heads towards protein and hydrophobic tails towards centre.  But due to lack of the facility of higher resolution power of electron microscope the actual assembly of protein and lipids could not revealed. ---2nm --3.5nm --2nm 22H. SINGH
  • 23.  The amount and types of vary greatly between different cells.  It was unable to describe how the proteins would allow the membrane to change shape without bonds being broken.  Membrane proteins are largely hydrophobic and therefore should not be found where the model positioned them. 23H. SINGH
  • 24.  In 1959, Robertson ,observed the structure in electron micrograph staining the tissues with osmium and saw Trilaminar appearance of membranes.  He saw no space for the pores in the micrograph. Osmium binds preferentially to the polar head groups of the lipid bilayer, producing the trilaminar.  The transverse sections of the membranes revealed the three-layer membrane structure known as the ‘railway’. In this view, which would later be called “Unit membrane”, there was a third layer between the two dense layers which was less dense pattern.  Robertson suggested that the dark regions were protein layers, while the open area in the middle was equivalent to the lipid layer  Though this model provided great insight into the structure of PM but functioning could not understand perfectly.  In 1964, Brady and Trams reported that membrane are composed of lipids and proteins, where proteins entered the membrane and the lipid components are fluid, that paved the way to development of Fluid Mosaic Model 24H. SINGH
  • 25.  With the development of freeze-breaking techniques and immuno-electron microscopy techniques, scientists identified isolated membrane proteins and membrane- embedded proteins through antibodies.  On the basis of their findings Singer and Nicolson introduced most accepted and famous FLUID MOSAIC MEMBRANE MODEL in 1972. “This model describe P M as a flexible boundary of the cell. It states that it is a lipid bilayer in which proteins occur as a ‘mosaic’ of discontinuous particles that penetrate irregularly deep or even through the lipid bilayer. Phospholipids molecules present in a fluid state and capable to move and rotate freely”. 25H. SINGH
  • 27.  According to this model,  It is ‘ fluid’ because phospholipid are free to move. Phospholipids in the lipid bilayer can either move rotationally, laterally in one bilayer, or occasionally undergo transverse movement (flip flop) between bilayers They can only move from side to side, however, not through the membrane. ▪ It is called a ‘ mosaic’ because the proteins are embedded in the phospholipid bilayer (like mosaic tiles embedded in mortar).  Hydrophilic portions of both proteins and phospholipids are maximally exposed to water resulting in a stable membrane structure. H. SINGH
  • 29. Transport: The plasma membrane regulates physically transporting substances from one side of the membrane to another, often from a region where the solute is at low concentration into a region of much higher concentration. It allows a cell to accumulate substances for metabolism and building macromolecules. A protein that spans the membrane may provide a hydrophilic channel ( aquaporins) across the membrane that is selective for a particular solute or porins for selected molecules. - 29H. SINGH
  • 30.  There are four broad categories of molecules found in the cellular environment. Some of these molecule can cross the membrane and some of them need the help of other molecules or processes.  hydrophilic Molecules are capable of forming bonds with water and other hydrophilic molecules, called polar molecules.  hydrophobic are called nonpolar molecules. Here are the 4 types:  Small, nonpolar molecules (ex: oxygen and carbon dioxide) can pass through the lipid bilayer and do so by squeezing through the phospholipid bilayers. They don't need proteins for transport and can diffuse across quickly.  Small, polar molecules (ex: water): water molecules diffuse through the membrane without the help of proteins but it slower process because the interior of the phospholipid bilayer is made up of the hydrophobic tails.  Large, nonpolar molecules (ex: carbon rings): These rings can pass through but it is also slow process.  Large, polar molecules (ex: simple sugar - glucose) and ions: The charge of an ion, and the size and charge of large polar molecules pass through the nonpolar region of the phospholipid membrane with the help of transmembrane proteins 30H. SINGH
  • 31. 1. Passive Transport: a) Simple Diffusion. b) Facilitated Diffusion 2. Active Transport: It may be - a) Primary active transport. b) Secondary Active transport 3. Bulk TRANSPORT: a) Endocytosis b) Exocytosis 31H. SINGH
  • 32.  (A) Passive Diffusion: Diffusion of nonpolar, hydrophobic molecules like Lipids from high to low concentration gradient /or  Simple diffusion through an aqueous channel (aquaporins)formed within an integral membrane protein or a cluster of such proteins. As in a, movement is always down a concentration gradient.  It does not required energy or membrane transport proteins.  e.g. transport of gases, ions and lipid soluble molecules 32H. SINGH
  • 33. ▪ Diffusion of molecules down the concentration gradient which required carrier proteins but does not require energy. ▪ Diffusion of hydrophilic molecules ,in which solute molecules bind specifically to a membrane protein carriers (facilitate transporters). ▪ Based on the direction of molecules it may be; ▪ a) Uniport: Transport of single type of molecule in one direction. ▪ B) Antiport: transport of molecules in opposite direction. 33H. SINGH
  • 34.  It is diffusion against concentration gradient from Low to high. Active transport by means of a protein transporter (protein pumps) with a specific binding site that undergoes a change through energy driven by ATP .  It may be: a) Primary Active transport: Transport against gradient in which energy(ATP) used directly. It requires carriers. e. g. sodium-potassium pump, calcium pump.  b) Secondary Active Transport: Transport against gradient in which energy (ATP) is used indirectly. Here tow or three molecules coupled e.g.NA-K and ATPase 34H. SINGH
  • 36.  Also called transport by vesicles formation, which involves formation of membrane bound vesicles.  It facilitates transport of macromolecules. Two Types: 1. Endocytosis : is when a cell ingests relatively larger contents than the single ions or molecules that pass through channels. It may be: a) Phagocytosis: engulfing of solid particles. b) Pinocytosis: engulfing of liquid particles. 2. Exocytosis : expulsing out of the molecules from the cell the cell membrane. The shape of the membrane itself changes to allow molecules to enter or exit the cell. 36H. SINGH
  • 37.  Passive osmosis and diffusion: transports gases (such as O2 and CO2) and other small molecules and ions  Transmembrane protein channels and transporters: transports small organic molecules such as sugars or amino acids  Endocytosis: transports large molecules (or even whole cells) by engulfing them  Exocytosis: removes or secretes substances such as hormones or enzymes 37H. SINGH
  • 38.  Some glycoprotein serve as identification tags that are specifically recognized by other cells.  Cells are able to recognize other through these tags.  Provide mechanisms for a cell to recognize itself and other cells of its particular individual organisms vs. non-self (foreign materials). 38H. SINGH
  • 39.  Membrane proteins of adjacent cell may be hooked together in various kinds of junction:  Plasmodesmata are junctions between plant cells, whereas animal cell contacts are carried out through tight junctions, gap junctions, and desmosomes.  A plasmodesma is a channel between the cell walls of two adjacent plant cells that allow materials to pass from the cytoplasm of one plant cell to the cytoplasm of an adjacent cell.  A tight junction is a watertight seal between two adjacent animal cells, which prevents materials from leaking out of cells.  Desmosomes connect adjacent cells when cadherins in the plasma membrane connect to intermediate filaments.  Gap junction (communicating junction), provide cytoplsamic channel for ions, nutrients and other substances that allow the cells to communicate. 39H. SINGH
  • 40.  Enzymatic activity ▪ Several enzymes in a membrane are ordered as a team that carries out sequential steps in metabolic pathway.  Signal transduction  The plasma membrane plays a critical role in the response of a cell to external stimuli such as a hormone, a process known as signal transduction.  Membranes possess receptor proteins that combine with specific molecules (ligands) or respond to other types of stimuli such as light or mechanical tension. 40H. SINGH
  • 41.  Microfilaments or other elements of the cytoskeleton may bonded to membrane proteins, a function that helps maintain cell shape and fixes the location of certain membrane proteins .  Protein that adhere to the ECM can coordinate extracellular and intracellular changes. (integrate changes occurring outside and inside the cell) Fibres of extracellular matrix (ECM) 41H. SINGH
  • 42.  Plasma Membranes are intimately involved in the processes by which one type of energy is converted to another type (energy transduction).  The most fundamental energy transduction occurs during photosynthesis when energy in sunlight is absorbed by membrane-bound pigments, converted into chemical energy, and stored in carbohydrates.  Membranes are also involved in the transfer of chemical energy from carbohydrates and fats to ATP. In eukaryotes, the machinery for these energy conversions is contained within membranes of chloroplasts and mitochondria. 42H. SINGH
  • 43.  The structure of Phospholipid responsible for the basic function of membranes as barriers between two aqueous compartments. Because the interior of the phospholipid bilayer is occupied by hydrophobic fatty acid chains, the membrane is impermeable to water-soluble molecules, including ions and most biological molecules. This protects all the components of the cell from the outside environment and allows separate activities to occur inside and outside the cell.  It also provides structural support to the cell. It tethers the cytoskeleton which is a network of protein filaments inside the cell that hold all the parts of the cell in place. 43H. SINGH
  • 44.  Plasma membranes are selectively permeable (or semi-permeable), meaning that only certain molecules can pass through them.  Water, oxygen, and carbon dioxide can easily travel through the membrane.  Generally, ions (e.g. sodium, potassium) and polar molecules cannot pass through the membrane; they must go through specific protein channels or pores in the membrane instead of freely diffusing through.  This way, the membrane can control the rate at which certain molecules can enter and exit the cell. 44H. SINGH
  • 45.  The plasma membrane may have extensions, such as whip-like flagella or brush-like cilia, that give it other functions.  In single-celled organisms, these membrane extensions may help the organisms to move.  In multicellular organisms, the extensions have different functions. 45H. SINGH
  • 46.  Plasma Membrane acts as physical barrier b/t extracellular environment and cytoplasm of the cell.  Gives the shape to the cell and protects the cell from external environment.  It is selectively permeable and hence regulates the transport of molecules. Lipid soluble molecules like O2 and CO2 and water can easily diffuse.  Different kinds of membrane proteins catalyze respective enzymatic activities  Participates in absorption, excretion and secretion.  It is responsible for intercellular communication.  It helps in maintaining the turgidity of the cell.  It serves as a receptor for various chemical stimuli such as amino acids, hormones, and sugars.  In certain unicellular organisms like amoeba, plasma membrane performs the function of ingestion of food (endocytosis) and locomotion too. It also facilitate exocytosis process  46H. SINGH
  • 47.  Cell membranes are dynamic (not static), fluid structure which held together by hydrophobic interactions.  Membrane fluidity can be affected by: a)The movement of phospholipids and some proteins. b) Phospholipids with unsaturated hydrocarbon tails maintain membrane fluidity at lower temperature. c) Length of fatty acyl chain. d) Presence of cholesterol/ sterol(plants). 47H. SINGH