Transport through Cell Membrane including passive transport and Active transport ,special types of passive transport , Special types of active transport , Dynamic motors, lipid layer and Protein Layer
endocytosis and exocytosis is a procss of cell eating and drinnking. it is a mazor tool for self defence to an individual cell. there are some molecular mechanism for this process described in given notes.
This presentation contains the introduction to the structure of plasma membrane. This gives an insight into the biochemistry of the plasma membrane and the singer and nicholsan model.
General overview of Plasma/ Cell membrane.
Definition of Plasma/ Cell membrane
Structure of Plasma membrane
1. Sandwitch model ORDanielli- Davson Model
2. Fluid mosaic model
Plasma Membrane Proteins
Chemical Composition of Plasma/ Cell Membrane
Movement across the Cell Membrane
Channels through cell membrane
Fluid Mosaic Model The fluid mosaic model describes the structure of the plasma membrane as a mosaic of components —including phospholipids, cholesterol, proteins, and carbohydrates—that gives the membrane a fluid character. ... The proportions of proteins, lipids, and carbohydrates in the plasma membrane
endocytosis and exocytosis is a procss of cell eating and drinnking. it is a mazor tool for self defence to an individual cell. there are some molecular mechanism for this process described in given notes.
This presentation contains the introduction to the structure of plasma membrane. This gives an insight into the biochemistry of the plasma membrane and the singer and nicholsan model.
General overview of Plasma/ Cell membrane.
Definition of Plasma/ Cell membrane
Structure of Plasma membrane
1. Sandwitch model ORDanielli- Davson Model
2. Fluid mosaic model
Plasma Membrane Proteins
Chemical Composition of Plasma/ Cell Membrane
Movement across the Cell Membrane
Channels through cell membrane
Fluid Mosaic Model The fluid mosaic model describes the structure of the plasma membrane as a mosaic of components —including phospholipids, cholesterol, proteins, and carbohydrates—that gives the membrane a fluid character. ... The proportions of proteins, lipids, and carbohydrates in the plasma membrane
Transport across cell membrane by Dr. TehmasTehmas Ahmad
Lecture about Transport of different substances across cell membrane. Continued from last two lectures. Lecture delivered on 26-Jan-2018 to First Year MBBS students in Bannu Medical College, Bannu.
Transport across cell membrane, CELL MEMBRANERajshri Ghogare
Transport across cell membrane, Active transport, Active transport,
Types of passive transport-Diffusion, Filtration, Osmosis, Facilitated diffusion , Types of active transport antiport and symport
Introduction of blood include properties of blood, functions of blood, hematocrit value , serum, plasma, plasma proteins, composition of blood ,composition of plasma
vitamin classification with fat soluble and water soluble vitamins ,vitamin A sources ,digestion, absorption along with biochemical functions, Recommended Dietary Intake, Deficiency, Hypervitaminosis
Attention Deficit disorder with its etiology, types and pathophysiology clinical features, Diagnosis, Assessment, differential Diagnosis and treatment , Medical Treatment and prognosis
Training of neuro Patients during pandemic is essential .physiotherapy include Relaxation Techniques, Brain training and most important Home Programm,Balance Training aa=nd gait training ,Diet Plan
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
2. INTRODUCTION
• All the cells in the body must be supplied with essential substances like nutrients, water,
electrolytes, etc.
• Cells also must get rid of many unwanted substances like waste materials, carbon dioxide,
etc.
• The cells achieve these by means of transport mechanisms across the cell membrane.
• Structure of the cell membrane is well suited for the transport of substances in and out of the
cell.
• Lipids and proteins of cell membrane play an important role in the transport of various
substances between extracellular fluid (ECF) and intracellular fluid (ICF).
4. PASSIVE TRANSPORT
• Passive transport is the transport of substances along the concentration gradient
or electrical gradient or both (electrochemical gradient).
• It is also known as diffusion or downhill movement.
• It does not need energy.
• Diffusion is of two types, namely
• Simple diffusion : Simple diffusion of substances occurs either through lipid
layer or protein layer of the cell membrane.
• Facilitated diffusion: Facilitated diffusion occurs with the help of the carrier
proteins of the cell membrane.
• Thus, the diffusion can be discussed under three headings:
1. Simple diffusion through lipid layer
2. Simple diffusion through protein layer
3. Facilitated or carrier-mediated diffusion.
5. SIMPLE DIFFUSION THROUGH LIPID
LAYER
•Lipid layer of the cell membrane is permeable only
to lipid-soluble substances like oxygen, carbon
dioxide and alcohol.
•The diffusion through the lipid layer is directly
proportional to the solubility of the substances in
lipids
6.
7. SIMPLE DIFFUSION THROUGH
PROTEIN LAYER
• Protein layer of the cell membrane is permeable to water-soluble substances.
• Mainly, electrolytes diffuse through the protein layer.
Protein Channels or Ion Channels
• Throughout the central lipid layer of the cell membrane, there are some pores.
• Integral protein molecules of protein layer invaginate into these pores from either surface of
the cell membrane.
• Thus, the pores present in the central lipid layer are entirely lined up by the integral protein
molecules.
• These pores form the channels for the diffusion of water, electrolytes and other substances,
which cannot pass through the lipid layer, these are called protein channels for water-
soluble substances.
8. Types of Protein Channels or Ion Channels
• Each channel can permit only one type of ion to pass through it.
• Accordingly, the channels are named after the ions which diffuse through these
channels such as sodium channels, potassium channels, etc.
Regulation of the Channels
• Some of the protein channels are continuously opened and most of the
channels are always closed.
• Continuously opened channels are called ungated channels
• Closed channels are called gated channels. These channels are opened only
when required
9. Gated Channels
Gated channels are divided into three categories:
i. Voltage-gated channels
ii. Ligand-gated channels
iii. Mechanically gated channels.
10. Voltage-gated channels
•Voltage-gated channels are the channels which
open whenever there is a change in the electrical
potential.
•For example, in the neuromuscular junction, when
action potential reaches axon terminal, the calcium
channels are opened and calcium ions diffuse into
the interior of the axon terminal from ECF.
11. Ligand-gated channels
• Ligand-gated channels are the type of channels which open in the
presence of some hormonal substances.
• The hormonal substances are called ligands and the channels are
called ligand-gated channels.
• During the transmission of impulse through the neuromuscular
junction, acetylcholine is released from the vesicles.
• The acetylcholine moves through the presynaptic membrane
(membrane of the axon terminal) and reaches the synaptic cleft.
• Then, the acetylcholine molecules cause opening of sodium channels
in the postsynaptic membrane and sodium ions diffuse into the
neuromuscular junction from ECF.
12. Mechanically gated channels
• Mechanically gated channels are the channels which are
opened by some mechanical factors.
• Examples are, channels present in the pressure receptors
(Pacinian corpuscles) and the receptor cells (hair cells) of
organ of Corti and vestibular apparatus.
• When a Pacinian corpuscle is subjected to pressure, it is
compressed resulting in deformation of its core fiber.
• This deformation causes opening of sodium channel and
development of receptor potential
13. FACILITATED OR CARRIERMEDIATED
DIFFUSION
• It is the type of diffusion by which the water-soluble substances having larger
molecules are transported through the cell membrane with the help of a carrier
protein.
• By this process, the substances are transported across the cell membrane faster
than the transport by simple diffusion.
• Glucose and amino acids are transported by facilitated diffusion.
• Glucose or amino acid molecules cannot diffuse through the channels because the
diameter of these molecules is larger than the diameter of the channels.
• Molecule of these substances binds with carrier protein.
• Now, some conformational change occurs in the carrier protein.
• Due to this change, the molecule reaches the other side of the cell membrane
14. FACTORS AFFECTING RATE OF DIFFUSION
• Permeability of the Cell Membrane: Rate of diffusion is directly proportional to the
permeability of cell membrane.
• Temperature: Rate of diffusion is directly proportional to the body temperature.
• Concentration Gradient or Electrical Gradient of the Substance across the Cell
Membrane: Rate of diffusion is directly proportional to the concentration gradient or electrical
gradient of the diffusing substances across the cell membrane
• Solubility of the Substance: Diffusion rate is directly proportional to the solubility of
substances
• Thickness of the Cell Membrane: Rate of diffusion is inversely proportional to the thickness
of the cell membrane.
• Size of the Molecules: Rate of diffusion is inversely proportional to the size of the molecules
• Size of the Ions:Generally, rate of diffusion is inversely proportional to the size of the ions.
• Charge of the Ions:Greater the charge of the ions, lesser is the rate of diffusion.
15. SPECIAL TYPES OF PASSIVE
TRANSPORT
In addition to diffusion, there are some special types of passive transport, viz.
1. Bulk flow: Bulk flow is the diffusion of large quantity of substances from a region of high pressure to
the region of low pressure due to the pressure gradient of the substance across the cell membrane.
• Eg: exchange of gases across the respiratory membrane in lungs.
2. Filtration: Movement of water and solutes from an area of high hydrostatic pressure to an area of low
hydrostatic pressure is called filtration.
• Eg : glomeruli of kidneys
3. Osmosis:It is defined as the movement of water or any other solvent from an area of lower
concentration to an area of higher concentration of a solute, through a semipermeable membrane
• permits the passage of only water or other solvents but not the solutes.
16.
17. Osmotic Pressure
• Osmotic pressure is the pressure created by the solutes in a fluid.
• During osmosis, when water or any other solvent moves from the area of lower concentration to the area of higher
concentration, the solutes in the area of higher concentration get dissolved in the solvent.
• This creates a pressure which is known as osmotic pressure.
Reverse Osmotic Pressure
• Reverse osmosis is a process in which water or other solvent flows in reverse direction (from the area of higher
concentration to the area of lower concentration of the solute.
Colloidal Osmotic Pressure and Oncotic Pressure
• The osmotic pressure exerted by the colloidal substances in the body is called the colloidal osmotic pressure.
• And, the osmotic pressure exerted by the colloidal substances (proteins) of the plasma is known as oncotic pressure
Types of Osmosis
Osmosis across the cell membrane is of two types:
1. Endosmosis: Movement of water into the cell
2. Exosmosis: Movement of water out of the cell.
18. ACTIVE TRANSPORT
• Active transport is the movement of substances against the chemical or electrical or electrochemical
gradient.
• It is also called uphill transport.
• Active transport requires energy, which is obtained mainly by breakdown of high energy compounds like
adenosine triphosphate (ATP).
CARRIER PROTEINS OF ACTIVE TRANSPORT
1. Uniport: Carrier protein that carries only one substance in a single direction is called uniport.
2. Symport or antiport:Symport or antiport is the carrier protein that transports two substances at a time.
• Carrier protein that transports two different substances in the same direction is called symport or symport
pump.
• Carrier protein that transports two different substances in opposite directions is called antiport or antiport
pump.
19. MECHANISM OF ACTIVE TRANSPORT
When a substance to be
transported across the cell
membrane comes near the
cell,
combines with
the carrier
protein of the
cell
membrane
forms substance-protein
complex
complex moves
towards the inner
surface of the cell
membrane.
substance is
released
from the
carrier
proteins
same carrier protein moves back to the
outer surface of the cell membrane
and transport
another molecule of
the substance.
20. TYPES OF ACTIVE TRANSPORT
Active transport is of two types:
1. Primary active transport: Primary active transport is the type of transport
mechanism in which the energy is liberated directly from the breakdown of ATP. By this
method, the substances like sodium, potassium, calcium, hydrogen and chloride are
transported across the cell membrane.
2. Secondary active transport.
21. Primary Active Transport of Sodium
and Potassium: Sodium-Potassium
Pump
• Sodium and potassium ions are transported across the cell
membrane by means of a common carrier protein called sodium-
potassium (Na+-K+) pump
• Also called Na+-K+ ATPase pump or Na+-K+ ATPase.
• Transports sodium from inside to outside the cell and potassium from
outside to inside the cell.
• Present in all the cells of the body.
• Responsible for the distribution of sodium and potassium ions across
the cell membrane and the development of resting membrane
potential.
22. Structure of Na+-K+ pump
• Made up of two protein subunit molecules, an α-subunit with a molecular weight of
100,000 and a β-subunit with a molecular weight of 55,000.
• Transport of Na+ and K+ occurs only by α-subunit.
• The β-subunit is a glycoprotein the function of which is not clear.
• α-subunit of the Na+-K+ pump has got six sites:
i. Three receptor sites for sodium ions on the inner (towards cytoplasm) surface of
the protein molecule
ii. Two receptor sites for potassium ions on the outer (towards ECF) surface of the
protein molecule
iii. One site for enzyme adenosine triphosphatase (ATPase), which is near the sites
for sodium.
23. Mechanism of action of Na+-K+ pump
• Three sodium ions from the cell get attached to the receptor sites of sodium ions on the inner
surface of the carrier protein.
• Two potassium ions outside the cell bind to the receptor sites of potassium ions located on
the outer surface of the carrier protein .
• Binding of sodium and potassium ions to carrier protein activates the enzyme ATPase.
• ATPase causes breakdown of ATP into adenosine diphosphate (ADP) with the release of one
high energy phosphate.
• Now, the energy liberated causes some sort of conformational change in the molecule of the
carrier protein.
• Because of this, the outer surface of the molecule (with potassium ions) now faces the inner
side of the cell.
• And, the inner surface of the protein molecule (with sodium ions) faces the outer side of the
cell .
• Now, dissociation and release of the ions take place so that the sodium ions are released
outside the cell (ECF) and the potassium ions are released inside the cell (ICF)..
24. SECONDARY ACTIVE TRANSPORT
• Secondary active transport is the transport of a substance with sodium ion, by means of a
common carrier protein.
• When sodium is transported by a carrier protein, another substance is also transported by
the same protein simultaneously, either in the same direction (of sodium movement) or in the
opposite direction.
• Thus, the transport of sodium is coupled with transport of another substance.
Secondary active transport is of two types:
1. Cotransport
2. Counter transport.
25. Electrogenic activity of Na+-K+ pump
Na+-K+ pump moves three sodium ions outside the cell and two potassium ions inside cell.
Thus, when the pump works once,
There is a net loss of one positively charged ion from the cell.
Continuous activity of the sodium-potassium pumps causes
Reduction in the number of positively charged ions inside the cell
Leading to increase in the negativity inside the cell.
Electrogenic activity of Na+-K+ pump.
26. Transport of Calcium Ions
• Calcium is actively transported from inside to outside the cell by
calcium pump. Calcium pump is operated by a separate carrier
protein.
• Energy is obtained from ATP by the catalytic activity of ATPase.
• Calcium pumps are also present in some organelles of the cell such
as sarcoplasmic reticulum in the muscle and the mitochondria of all
the cells.
• These pumps move calcium into the organelles.
27. Transport of Hydrogen Ions
• Hydrogen ion is actively transported across the cell membrane by the carrier protein called
hydrogen pump.
• It also obtains energy from ATP by the activity of ATPase.
• The hydrogen pumps that are present in two important organs have some functional
significance.
1. Stomach: Hydrogen pumps in parietal cells of the gastric glands are involved in the formation
of hydrochloric acid
2. Kidney: Hydrogen pumps in epithelial cells of distal convoluted tubules and collecting ducts
are involved in the secretion of hydrogen ions from blood into urine
28. SECONDARY ACTIVE TRANSPORT
• Secondary active transport is the transport of a substance with sodium ion, by means of a
common carrier protein.
• When sodium is transported by a carrier protein, another substance is also transported by the
same protein simultaneously, either in the same direction (of sodium movement) or in the
opposite direction.
• Thus, the transport of sodium is coupled with transport of another substance.
Secondary active transport is of two types:
1. Cotransport
2. Counter transport.
29. Sodium Cotransport
• Sodium cotransport is the process in which, along with sodium, another substance
is transported by a carrier protein called symport.
• Energy for movement of sodium is obtained by breakdown of ATP.
• And the energy released by the movement of sodium is utilized for movement of
another substance.
• Substances carried by sodium cotransport are glucose, amino acids, chloride,
iodine, iron and urate.
Carrier protein for sodium cotransport
• Carrier protein for the sodium cotransport has two receptor sites on the outer
surface.
• Among the two sites, one is for binding of sodium and another site is for binding of
other substance.
30. Sodium cotransport of glucose
• One sodium ion and one glucose molecule from the ECF bind with the respective receptor
sites of carrier protein of the cell membrane.
• Now, the carrier protein is activated.
• It causes conformational changes in the carrier protein, so that sodium and glucose are
released into the cell
31. Sodium cotransport of amino acids
• Carrier proteins for the transport of amino acids are different
from the carrier proteins for the transport of glucose.
• For the transport of amino acids, there are five sets of
carrier proteins in the cell membrane.
• Each one carries different amino acids depending upon the
molecular weight of the amino acids.
• Sodium cotransport of amino acids also occurs during the
absorption of amino acids from the intestine and
reabsorption from renal tubule.
32. Sodium counter transport.
A. Na+ from ECF and H+ from ICF bind with carrier protein;
B. Conformational change occurs in the carrier protein;
C. Na+ enters ICF and H+ enters ECF.
Sodium cotransport and counter transport
by carrier proteins
33. Sodium Counter Transport
• Sodium counter transport is the process by which the substances are
transported across the cell membrane in exchange for sodium ions by
carrier protein called antiport.
• Various counter transport systems are:
i. Sodium-calcium counter transport: In this, sodium and calcium ions
move in opposite directions with the help of a carrier protein.
ii. Sodium-hydrogen counter transport: In this system, the hydrogen ions
are exchanged for sodium ions and this occurs in the renal tubular cells.
Other counter transport systems: Other counter transport systems are
sodium-magnesium counter transport, sodium-potassium counter transport,
calcium-magnesium counter transport, calcium-potassium counter transport,
chloride bicarbonate counter transport and chloride sulfate counter transport.
34. SPECIAL TYPES OF ACTIVE
TRANSPORT
• In addition to primary and secondary active transport
systems, there are some special categories of active
transport which are generally called the vesicular transport.
Special categories of active transport:
1. Endocytosis
2. Exocytosis
3. Transcytosis.
35. ENDOCYTOSIS
• Endocytosis is defined as a transport mechanism by which the macromolecules enter the
cell.
• Macromolecules (substances with larger molecules) cannot pass through the cell membrane
either by active or by passive transport mechanism.
• Such substances are transported into the cell by endocytosis.
Endocytosis is of three types:
1. Pinocytosis
2. Phagocytosis
3. Receptor-mediated endocytosis.
1. Pinocytosis
• Pinocytosis is a process by which macromolecules like bacteria and antigens are taken into
the cells.
• It is otherwise called the cell drinking.
36. Macromolecules (in the form of droplets of fluid)
bind to the outer surface of the cell membrane
ii. Now, the cell membrane evaginates around the
droplets
iii. Droplets are engulfed by the membrane
iv. Engulfed droplets are converted into vesicles and
vacuoles, which are called endosomes
v. Endosome travels into the interior of the cell
vi. Primary lysosome in the cytoplasm fuses with
endosome and forms secondary lysosome
vii. Now, hydrolytic enzymes present in the
secondary lysosome are activated resulting in
digestion and degradation of the endosomal
contents
37. Phagocytosis
• Phagocytosis is the process by which particles larger than the macromolecules are engulfed
into the cells.
• It is also called cell eating.
• Larger bacteria, larger antigens and other larger foreign bodies are taken inside the cell by
means of phagocytosis.
• Only few cells in the body like neutrophils, monocytes and the tissue macrophages show
phagocytosis.
• Among these cells, the macrophages are the largest phagocytic cells.
38. Mechanism of phagocytosis
i.When bacteria or
foreign body enters
the body, first the
phagocytic cell sends
cytoplasmic extension
(pseudopodium)
around bacteria or
foreign body
ii.Then, these
particles are engulfed
and are converted into
endosome like
vacuole.
Vacuole is very large
and it is usually called
the phagosome
iii. Phagosome travels
into the interior of cell
iv. Primary lysosome
fuses with this
phagosome and forms
secondary lysosome
v. Hydrolytic enzymes
present in the
secondary lysosome
are activated resulting
in digestion and
degradation of the
phagosomal contents
39. Receptor-mediated Endocytosis
• Receptor-mediated endocytosis is the transport of macromolecules with the help of a
receptor protein.
• Surface of cell membrane has some pits which contain a receptor protein called clathrin.
Together with a receptor protein (clathrin), each pit is called receptor-coated pit.
• These receptor-coated pits are involved in the receptormediated endocytosis
40. Mechanism of receptor-mediated
endocytosis
i. Receptor-mediated endocytosis is induced by substances like ligands
ii. Ligand molecules approach the cell and bind to receptors in the coated pits and form ligand
receptor complex
iii. Ligand-receptor complex gets aggregated in the coated pits.Then, the pit is detached from cell
membrane and becomes the coated vesicle.This coated vesicle forms the endosome
iv. Endosome travels into the interior of the cell. Primary lysosome in the cytoplasm fuses with
endosome and forms secondary lysosome
v. Now, the hydrolytic enzymes present in secondary lysosome are activated resulting in release of
ligands into the cytoplasm
vi. Receptor may move to a new pit of the cell membrane
41.
42. EXOCYTOSIS
• Exocytosis is the process by which the substances are expelled from the cell. In this process, the substances are
extruded from cell without passing through the cell membrane.
• This is the reverse of endocytosis.
Mechanism of Exocytosis
• Exocytosis is involved in the release of secretory substances from
cells.
• Secretory substances of the cell are stored in the form of secretory
vesicles in the cytoplasm.
• When required, the vesicles approach the cell membrane and get fused with the cell membrane.
• Later, the contents of the vesicles are released out of the cell .
Role of Calcium in Exocytosis
• Calcium ions play an important role during the release of some secretory substances such as neurotransmitters.
• The calcium ions enter the cell and cause exocytosis.
43. TRANSCYTOSIS
• Transcytosis is a transport mechanism in which an extracellular macromolecule enters
through one side of a cell, migrates across cytoplasm of the cell and exits through the other
side.
Mechanism of Transcytosis
• Cell encloses the extracellular substance by invagination of the cell membrane to form a
vesicle.
• Vesicle then moves across the cell and thrown out through opposite cell membrane by means
of exocytosis.
• Transcytosis involves the receptor-coated pits as in receptor-mediated endocytosis.
• Receptor protein coating the pits in this process is caveolin and not clathrin.
• Transcytosis is also called, vesicle trafficking or cytopempsis.
44. MOLECULAR MOTORS
MOLECULAR MOTORS
Molecular motors are the protein-based molecular machines that perform intracellular movements in response to
specific stimuli.
„FUNCTIONS OF MOLECULAR MOTORS
1. Transport of synaptic vesicles containing neurotransmitters from the nerve cell body to synaptic terminal
2. Role in cell division (mitosis and meiosis) by pulling the chromosomes
3. Transport of viruses and toxins to the interior of the cell for its own detriment.
„TYPES OF MOLECULAR MOTORS
Molecular motors are classified into three super amilies:
1. Kinesin
2. Dynein
3. Myosin.
45. Kinesin
• Kinesin transports substances by moving over the microtubules.
• Each kinesin molecule has two heads and a tail portion.
• One of the heads hydrolyses ATP to obtain energy.
• By utilizing this energy, the other head swings continuously causing
movement of the whole kinesin molecule .
• End portion of the tail carries the cargo (substances to be
transported).
• Kinesin is responsible for anterograde transport (transport of
substances towards the positive end of microtubule).
46. Dynein
•Dynein is almost similar to kinesin and
transports substances by moving over the
microtubules.
•But it is responsible for retrograde transport
(transport of substances towards the negative
end of microtubule).
47. Myosin
• Myosin transports substances by moving over micro
filaments.
• Myosins are classified into 18 types according to the amino
acid sequence.
• However, myosin II and V are functionally significant.
Myosin II is involved in
• muscle contraction .
• Myosin V is involved in transport of vesicles.