Structure and function of plasma membrane 2ICHHA PURAK
The presentation consists of 72 slides,describes following heads
DEFINITION : STRUCTURE OF PLASMA MEMBRANE
COMPONENTS OF PLASMA MEMBRANE ( (BIOCHEMICAL PROPERTIES)
LIPID BILAYER
PROTEINS
CARBOHYDRATES
CHOLESTEROL
MODELS EXPLAINING STRUCTURE OF BIO MEMBRANE
FLUID MOSAIC MODEL
MOBILITY OF MEMBRANE
GLYCOCALYX : GLYCOPROTEINS AND GLYCOLIPIDS
TRANSPORT OF IONS AND MOLECULES ACROSS PLASMA MEMBRANE
FUNCTIONS OF PLASMA MEMBRANE
DIVERSITY OF CELL MEMBRANES
SITE OF ATPASE ION CARRIER CHANNELS AND PUMPS-RECEPTORS
a deeply explained process of cell division, for understanding it thoroughly. i tried to put in all the information i knew and collected. i hope it is helpful or you.
Infer the significance of cell division.
Differentiate a DNA molecule, a chromosome, and a chromatid.
Characterize the phases of the cell cycle and their control points.
Describe the major events associated with stages of mitosis.
Explain the process of cytokinesis.
Learning Objectives
Describe the role of apoptosis in the life cycle of a cell.
Relate cancer as a result of the malfunction of the cell during the cell cycle.
Structure and function of plasma membrane 2ICHHA PURAK
The presentation consists of 72 slides,describes following heads
DEFINITION : STRUCTURE OF PLASMA MEMBRANE
COMPONENTS OF PLASMA MEMBRANE ( (BIOCHEMICAL PROPERTIES)
LIPID BILAYER
PROTEINS
CARBOHYDRATES
CHOLESTEROL
MODELS EXPLAINING STRUCTURE OF BIO MEMBRANE
FLUID MOSAIC MODEL
MOBILITY OF MEMBRANE
GLYCOCALYX : GLYCOPROTEINS AND GLYCOLIPIDS
TRANSPORT OF IONS AND MOLECULES ACROSS PLASMA MEMBRANE
FUNCTIONS OF PLASMA MEMBRANE
DIVERSITY OF CELL MEMBRANES
SITE OF ATPASE ION CARRIER CHANNELS AND PUMPS-RECEPTORS
a deeply explained process of cell division, for understanding it thoroughly. i tried to put in all the information i knew and collected. i hope it is helpful or you.
Infer the significance of cell division.
Differentiate a DNA molecule, a chromosome, and a chromatid.
Characterize the phases of the cell cycle and their control points.
Describe the major events associated with stages of mitosis.
Explain the process of cytokinesis.
Learning Objectives
Describe the role of apoptosis in the life cycle of a cell.
Relate cancer as a result of the malfunction of the cell during the cell cycle.
this presentation has detailed information on cell cycle. it includes steps as well as how the proteins take part in cell cycle.
i have also added information on some experiments that were carried out.
happy studying :)
Extra cellular matrix is recently being explored in connection with cancer , metastases and autoimmune disorders. It is prepared for the benefit of both UG and PG medical and dental students.
The sequence of events cell division, DNA replication and cell growth by which a cell duplicates its genome, eventually divides into two daughter cells is termed cell cycle.
this presentation has detailed information on cell cycle. it includes steps as well as how the proteins take part in cell cycle.
i have also added information on some experiments that were carried out.
happy studying :)
Extra cellular matrix is recently being explored in connection with cancer , metastases and autoimmune disorders. It is prepared for the benefit of both UG and PG medical and dental students.
The sequence of events cell division, DNA replication and cell growth by which a cell duplicates its genome, eventually divides into two daughter cells is termed cell cycle.
OVERVIEW OF CELL CYCLE
Explained in brief phases of cell cycle . Given a explanation of each phase in detail, also explained the significance of meiosis in brief.
The study of the cell cycle focuses on mechanisms that regulate the timing and frequency of DNA duplication and cell division. As a biological concept, the cell cycle is defined as the period between successive divisions of a cell. During this period, the contents of the cell must be accurately replicated.
The cell cycle is regulated by cyclins and cyclin-dependent kinases.
How long is one cell cycle?
Depends. Eg. Skin cells every 24 hours. Some bacteria every 2 hours. Some cells every 3 months. Cancer cells very short. Nerve cells never.
Programmed cell death:
Each cell type will only do so many cell cycles then die. (Apoptosis)
The sequence of events by which a cell duplicates its genome, synthesizes the other constituents of the cell and eventually divides into two daughter cells is termed cell cycle
ntry points of glucogenicamino acids after transamination
are indicated by arrows extended from circles
the key gluconeogenicenzymes are enclosed in double
bordered boxes. oated fashion. They are interdependent; each forms a strand in the web of life. Parasitology is
the science that deals with organisms living in the human body (the host) and the medical significance of
this host-parasite relationship.
ASSOCIATION BETWEEN PARASITE AND HOST
A parasite is a living organism, which takes its nourishment and other needs from ahost; the host is an
organism which supports the parasite. The hosts vary depending on whether they harbor the various
stages in parasitic development
DIFFERENT KINDS OF PARASITES
Ectoparasite – a parasitic organism that lives on the outer surface of its host, e.g. lice, ticks, mites etc.
Endoparasites parasites that live inside the body of their host, e.g. Entamoeba histolytica.
Obligate Parasite- This parasite is completely dependent on the host during a segment or all of its life
cycle, e.g. Plasmodium spp.
Facultative parasite – an organism that exhibits both parasitic and non-parasitic modes of living and
hence does not absolutely depend on the parasitic way of life but is capable of adapting to it if paced on
a host. E.g. Naegleria fowleri
Accidental parasite – when a parasite attacks an unnatural host and survives. E.g. Hymenolepis diminuta
(rat tapeworm).
Erratic parasite - is one that wanders in to an organ in which it is not usually found. E.g. Entamoeba
histolytica in the liver or lung of humans.
Most of the parasites which live in/on the body of the host do not cause disease (non-pathogenic
parasites). In Medical parasitology we focus on most of the disease causing (pathogenic) parasites.
However, understanding parasites which do not ordinariy produce disease in heathy
(immunocompetent) individuals but do cause illness in individuals with impaired defense mechanism
(opportunistic parasites) is becoming of paramount importance because of the increasing prevaence of
HIV/AIDS in our country.
DIFFERENT KINDS OF HOSTS
Definitive host – a host that harbors a parasite in the adult stage or where the parasite undergoes a
sexual method of reproduction.
Intermediate host - harbors the arval stages of the parasite or an asexual cycle of development takes
pace. In some cases, larval development is completed in two different intermediate hosts, referred to
as first and second intermediate hosts.
Paratenic host – a host that serves as a temporary refuge and vehicle for reaching an obligatory host,
usually the definitive host, i.e. it is not necessary for the completion of the parasites life cycle.
Reservoir host – a host that makes the parasite available for the transmission to another host and is
usually not affected by the infection.
Natural host a host that is naturally infected with certain species of parasite.
Accidental host – a host that is under normal circumstances not infected with th
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
2. Cell cycle
• The sequence of events by which a cell duplicates its genome, synthesizes
the other constituents of the cell and eventually divides into two daughter
cells is termed cell cycle.
• During the division of a cell, DNA replication and cell growth take place in
a organized way to ensure correct division and formation of progeny cells
containing whole genomes.
• Due to cell division , a new organism is formed from existing one,
multicellular organism grows up and emaciated body can be restored.
3. Types of cell division
• There are two types of cell division as mitosis and meiosis.
• Mitosis occurs in somatic cells and stem cells of the body whereas
meiosis occurs in germ cells.
• Before any type of cell division, the cell doubles up its chromosome
number present in its nucleus i.e. if chromosome number is 2n, it is
doubled up to 4n.
4. • A pair of each type of chromosome is present in 2n condition
whereas single chromosome of each type is present in n condition.
5.
6. Mitosis: Cell division phases
• The cell cycle is divided into two basic phases:
• l. Interphase
• II. M Phase (Mitosis phase)
• The interphase lasts more than 95% of the duration of cell cycle.
• The interphase, though called the resting phase, is the time during which the
cell is preparing for division by undergoing both cell growth and DNA
replication in an orderly manner.
• The interphase is divided into three further phases:
• l. G1 phase (Gap 1)
• II. S phase (Synthesis)
• III.G2 phase (Gap 2)
7. G1 phase
• G1 phase corresponds to the interval between mitosis and initiation
of DNA replication.
• During G1 phase the cell is metabolically active and continuously
grows but does not replicate its DNA.
8. S phase
• S or synthesis phase marks the period during which DNA
synthesis or replication takes place.
• During this time the amount of DNA per cell doubles. If the
initial amount of DNA is denoted as 2C then it increases to
4C.
• However, there is no increase in the chromosome number.
• In animal cells, during the S phase, DNA replication begins in
the nucleus, and the centriole duplicates in the cytoplasm.
9. G2 PHASE
• During the G2 phase, proteins are synthesized in preparation for
mitosis while cell growth continues.
10. G0 STAGE
• Some cells in the adult animals do not appear to exhibit division (e.g.,
heart cells) and many other cells divide only occasionally, as needed
to replace cells that have been lost because of injury or cell death.
• These cells that do not divide further exit G1 phase to enter an
inactive stage called quiescent stage (G0) of the cell cycle.
• Cells in this stage remain metabolically active but no longer
proliferate unless called on to do so depending on the requirement of
the organism.
11. M Phase
• The M Phase represents the phase when the actual cell division or
mitosis occurs, it is also called as equational division.
• The M Phase starts with the nuclear division, corresponding to the
separation of daughter chromosomes (karyokinesis) and usually ends
with division of cytoplasm (cytokinesis).
12. • Though for convenience mitosis has been divided into four stages of
nuclear division (karyokinesis).
• Prophase
• Metaphase
• Anaphase
• Telophase
13.
14. Prophase
• Chromosomal material condenses to form compact mitotic
chromosomes.
• Chromosomes are seen to be composed of two sister chromosomes
attached together at the centromere.
• Centrosome which had undergone duplication during interphase,
begins to move towards opposite poles of the cell.
• Each centrosome radiates out microtubules called asters. The two
asters together with spindle fibres forms mitotic apparatus.
• Cells at the end of prophase, when viewed under the microscope, do
not show Golgi complexes, endoplasmic reticulum, nucleolus and the
nuclear envelope.
15.
16. Metaphase
• Spindle fibres attach to kinetochores of chromosomes.
• Chromosomes are moved to spindle equator and get aligned along
metaphase plate through spindle fibres to both poles.
21. Telophase
• Chromosomes cluster at opposite spindle poles and their identity is
lost as discrete elements.
• Nuclear envelope develops around the chromosome clusters at each
pole forming two daughter nuclei.
• Nucleolus, Golgi complex and ER reform.
22.
23. Cytokinesis
• Cytokinesis is the physical process of cell division, which divides the
cytoplasm of a parental cell into two daughter cells.
• In an animal cell, this is achieved by the appearance of a furrow in the
plasma membrane. The furrow gradually deepens and ultimately joins in the
center dividing the cell cytoplasm into two.
• At the time of cytoplasmic division, organelles like mitochondria and plastids
get distributed between the two daughter cells.
• In some organisms karyokinesis is not followed by cytokinesis as a result of
which multinucleate condition arises leading to the formation of syncytium
(e.g., liquid endosperm in coconut).
• Mitosis is essential for growth of the body. Besides, it is necessary for
restoration of emaciated body, wound healing, formation of blood cells, etc.
24.
25. Meiosis
• Cell division that reduces the chromosome number by half results in the
production of haploid daughter cells called meiosis.
• Meiosis ensures the production of haploid phase in the life cycle of
sexually reproducing organisms whereas fertilisation restores the diploid
phase.
• Meiosis involves two sequential cycles of nuclear and cell division called
meiosis I and meiosis II but only a single cycle of DNA replication
26. • Meiosis is completed through two stages. Those two stages are
meiosis-I and meiosis-II.
• In meiosis-I, recombination / crossing over occur between
homologous chromosomes and thereafter those homologous
chromosomes (Not sister chromatids) are divided into two groups and
thus two haploid cells are formed.
27. MEOSIS –I
• Prophase I: Prophase of the first meiotic division is typically longer and
more complex when compared to prophase of mitosis.
• It has been further subdivided into the following five phases based on
chromosomal behavior,
• Leptotene
• Zygotene
• Pachytene
• Diplotene
• Diakinesis
28. • During leptotene stage the chromosomes become gradually visible
(CONDENSATION) under the light microscope.
• The compaction of chromosomes continues throughout leptotene.
zygotene
• During this stage chromosomes start pairing together and this process of
association is called synapsis. Such paired chromosomes are called
Homologous chromosomes.
• Chromosome synapsis is accompanied by the formation of complex
structure called synaptonemal complex.
• The complex formed by a pair of synapsed homologous chromosomes is
called a Bivalent or a tetrad.
29. Pachytene
• During this stage, the four chromatids of each bivalent chromosomes
becomes distinct and clearly appears as tetrads.
• This stage is characterized by the appearance of recombination nodules, the
sites at which crossing over occurs between non-sister chromatids of the
homologous chromosomes.
• Crossing over is the exchange of genetic material between two homologous
chromosomes.
30.
31. Diplotene
• This stage is recognised by the dissolution of the synaptonemal
complex and the tendency of the recombined homologous
chromosomes of the bivalents to separate from each other except at
the sites of crossovers.
• These X-shaped structures, are called chiasmata.
• In oocytes of some vertebrates, diplotene can last for months or
years.
32.
33. Diakinesis
• This is marked by terminalisation of chiasmata.
• During this phase the chromosomes are fully condensed and the
meiotic spindle is assembled to prepare the homologous
chromosomes for separation.
• By the end of diakinesis, the nucleolus disappears and the nuclear
envelope also breaks down.
• Diakinesis represents transition to metaphase.
34. Metaphase I
• The bivalent chromosomes align on the equatorial plate.
• The microtubules from the opposite poles of the spindle attach to the
kinetochore of homologous chromosomes.
35. Anaphase I
• The homologous chromosomes separate, while sister chromatids
remain associated at their centromeres.
36. Telophase I
• The nuclear membrane and nucleolus reappear, cytokinesis follows and
this is called as dyad of cells.
• Although in many cases the chromosomes do undergo some dispersion,
they do not reach the extremely extended state of the interphase
nucleus.
• The stage between the two meiotic divisions is called interkinesis and is
generally short lived.
• There is no replication of DNA during interkinesis. Interkinesis is
followed by prophase II, a much simpler prophase than prophase I.
37. Meiosis II
• Prophase II: Meiosis II is initiated immediately after cytokinesis, usually before
the chromosomes have fully elongated.
• In contrast to meiosis I, meiosis II resembles a normal mitosis. The nuclear
membrane disappears by the end of prophase II.
• The chromosomes again become compact.
• Metaphase II: At this stage the chromosomes align at the equator and the
microtubules from opposite poles of the spindle get attached to the
kinetochores of sister chromatids.
• Anaphase II: It begins with the simultaneous splitting of the centromere of
each chromosome (which was holding the sister chromatids together), allowing
them to move toward opposite poles of the cell by shortening of microtubules
attached to kinetochores.