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Anindita Bhadra
E-mail: abhadra@iiserkol.ac.in
A Generalized Cell
Proteins
Phospholipids
Phospholipids
Proteins
Hydrocarbon tails
1. Transport
2. Enzyme
3. Receptor sites
4. Intercellular junctions
5. Cell-cell recognition
6. Cytoskeletal and extracellular
matrix attachment
Other Molecules
Carbohydrates can be
associated with the exterior
surface of the membrane.
Cholesterol - stiffens the
membrane by connecting
phospholipids
Glycolipids - signal molecules
Glycoproteins - have an
attached chain of sugar
(antibodies)
Membrane Proteins
Channel Proteins: form small openings for molecules to
diffuse through
Carrier Proteins: regulate transport and diffusion
Receptor Proteins: molecular triggers that set off cell
responses (such as release of hormones or opening of
channel proteins)
Cell Recognition Proteins: Marker proteins that identify
the cell to other cells
Enzymatic Proteins: carry out metabolic reactions
Transport Proteins
Carrier proteins are peripharal proteins which do
not extend all the way through the membrane. They
bond and drag molecules through the bilipid layer
and release them on the opposite side, one at a time.
Transport Proteins
Symports also use the process of diffusion. In this case
a molecule that is moving naturally into the cell through
diffusion is used to drag another molecule into the cell.
For example, glucose hitches a ride with sodium.
Some proteins actively use energy from the ATPs in the cell to drag molecules
from area of low concentration to areas of high concentration (working directly
against diffusion) an example of this is the sodium/potassium pump. Here the
energy of a phosphate (shown in red) is used to exchange sodium atoms for
potassium atoms.
Marker Proteins
Marker proteins extend across the cell membrane
and serve to identify the cell.
The immune system uses these proteins to tell
friendly cells from foreign invaders.
They are as unique as fingerprints.
They play an important role in organ transplants. If the marker proteins on a
transplanted organ are different from those of the original organ the body will
reject it as a foreign invader.
Endocytosis
An important group of peripheral membrane proteins are water-soluble
enzymes that associate with the polar head groups of membrane phospholipids.
One well-understood group of such enzymes are the phospholipases, which
hydrolyze various bonds in the head groups of phospholipids.
These enzymes have an important role in the degradation of damaged or aged
cell membranes.
Large molecules that are manufactured in the cell are released through the cell
membrane by the reverse process, called exocytosis.
Endocytosis
The cell membrane can also
engulf structures that are much
too large to fit through the
pores in the membrane proteins.
This process is known as
endocytosis.
In this process the membrane
itself wraps around the particle
and pinches off a vesicle inside
the cell.
Cell Organelles
Anindita Bhadra
E-mail: abhadra@iiserkol.ac.in
Cytoskeleton
The cytoskeleton is a system of protein filaments in the cytoplasm of a eukaryotic
cell that gives the cell shape and the capacity for directed movement.
Intermediate filaments provide mechanical strength.
Microtubules determine the positions of membrane bound organelles and direct
intracellular transport.
Actin filaments determine the shape of the cells surface and are necessary for
whole-cell locomotion.
A large number of accessory proteins are associated with these filaments.
Cytoskeleton
Each type of cytoskeletal filament is constructed from smaller protein subunits.
The cell is able to build large cytoskeletal structures by the repetitive assembly of
large numbers of the small protein subunits.
Because these subunits are small, they can diffuse rapidly within cytoplasm,
whereas the assembled filaments cannot.
In this way, cells can undergo rapid structural reorganizations, disassembling
filaments at one site and reassembling them at another site far away
Cytoskeleton
Each type of cytoskeletal filament is constructed from smaller protein subunits.
The cell is able to build large cytoskeletal structures by the repetitive assembly of
large numbers of the small protein subunits.
Because these subunits are small, they can diffuse rapidly within cytoplasm,
whereas the assembled filaments cannot.
In this way, cells can undergo rapid structural reorganizations, disassembling
filaments at one site and reassembling them at another site far away
Endoplasmic Reticulum
The ER consists of membranous channels that wind through the cytoplasm.
It is the transport network for molecules targeted for certain modifications and
specific final destinations, as opposed to molecules that are destined to float
freely in the cytoplasm.
There are two types of ER, rough and smooth. Rough ER has ribosomes attached
to it, and smooth ER does not.
Rough ER produces proteins, smooth ER produces steroids.
Ribosomes
The ribosomes are the sites of protein synthesis in the cell.
They are mostly attached to the ER, but some are also free, in the cytoplasm.
A ribosome, formed from two subunits locking together, functions to:
(1) Translate encoded information from the cell nucleus provided by messenger
ribonucleic acid (mRNA),
(2) Link together amino acids selected and collected from the cytoplasm by
transfer ribonucleic acid (tRNA),
(3) Export the polypeptide produced to the cytoplasm where it will form a
functional protein.
Ribosomes
The proteins produced by the free ribosomes are mostly used within the cell,
while those produced by the ribosomes on the ER are transported out.
In a mammalian cell there can be as many as 10 million ribosomes.
Several ribosomes can be attached to the same mRNA strand, this structure is
called a polysome.
Ribosomes have only a temporary existence. When they have synthesised a
polypeptide the two sub-units separate and are either re-used or broken up.
Ribosomes
Ribosomes can join up amino acids at a rate of 200 per minute.
Ribosomes are organelles composed of ribosomal proteins (riboproteins) and
ribonucleic acids (ribonucleoproteins).
A eukaryotic ribosome is composed of ribosomal RNA and about 80 proteins
and has a molecular mass of about 4,200,000 Da.
Ribosomes are found in prokaryotic cells, eukaryotic cells, chloroplasts and
mitochondria.
Ribosomes
There are about 10 billion protein molecules in a mammalian cell and ribosomes
produce most of them.
The proteins and nucleic acids that form the ribosome sub-units are made in the
nucleolus and exported through nuclear pores into the cytoplasm.
The two sub-units are unequal in size and exist in this state until required for
use.
The larger sub-unit has mainly a catalytic function; the smaller sub-unit mainly a
decoding one.
Vesicles
Vesicles are double membrane bound sacs carrying different products from one
part of the cell to another.
They are often associated with the Golgi apparatus.
They also carry food, enzymes, waste products.
They are involved in storage, transport and phagocytosis.
Lysosomes and peroxisomes are two kinds of vesicles found in the cell.
Mitochondrion
The mitochondrion is the site of cellular respiration.
The mitochondrion is a double membrane bound structure filled with a fluid
matrix.
The outer membrane is selectively permeable, just like the cell membrane.
The inner membrane is folded inward to provide extra surfaces for cellular
respiration.
These folds are known as cristae.
Mitochondrion
The inner membrane is freely permeable only to oxygen, carbon dioxide, and
water.
The inter-membrane space has an important role in the primary function of
mitochondria, which is oxidative phosphorylation.
The matrix contains dissolved oxygen, water, carbon dioxide, the recyclable
intermediates that serve as energy shuttles, enzymes etc.
Mitochondria produce adenosine triphosphate (ATP) by systematically
extracting energy from nutrient molecules (substrates).
Vacuole
Vacuoles serve a variety of functions, including storage.
They have an irregular shape and are usually very large in plant cells, occupying
30 90% of the cell volume.
They contribute to the rigidity of the plant using water to develop hydrostatic
pressure.
They also store nutrient and non-nutrient chemicals and break down complex
molecules.
Nucleus
Most eukaryotic cells contain a nucleus, which is seen under the microscope as a
dark mass inside the cell.
The nucleus is surrounded by a double membrane, known as the nuclear
envelope.
A fluid-filled space or perinuclear space is present between the two layers of a
nuclear membrane.
The nuclear envelope is a highly regulated membrane barrier that allows the
compartmentalisation of the nucleus from the cytoplasm.
Nucleus
Nuclear pore complexes (NPCs) are large proteinaceous channels that perforate
the nuclear membrane and allow transport of molecules in and out of the
nucleus.
Nucleoplasm, also known as karyoplasm, is the matrix present inside the
nucleus.
Genes are located in chromosomes inside the nucleus.
The nucleus is the site of DNA replication and transcription.
Nucleus
The DNA is transcribed into premessenger RNA (premRNAs) inside the
nucleus. The mature mRNA after splicing is exported to the cytoplasm for
translation.
The clearest substructure in the nucleus in most eukaryotes is the nucleolus,
which is the site of rDNA transcription and ribosome biosynthesis.
The nucleolus is the largest structure in the cell nucleus.
The nucleolus has numerous other functions including assembly of signal
recognition particles, modification of transfer RNAs and sensing cellular stress.
Nucleus
The nucleolus disappears when a cell undergoes division and is reformed after
the completion of cell division.
Nuclear speckles are highly dynamic, irregularly shaped nuclear domains
enriched with premRNA splicing factors.
One of the earliest ideas about the evolution of the eukaryotic cell was that
organelles formed when the plasma membrane grew into the cell and started
walling off parts of the cell. This idea, called the autogenic hypothesis, may
correctly explain the origin of the nuclear membrane, endoplasmic reticulum,
and Golgi apparatus.
Nucleus
Exceptions to the rule:
Multinucleated cells: Mammalian skeletal muscle cells; plasmodia of slime
molds; metastatizing tumor cells.
Enucleated cells: Mammalian red blood cells.
Dolly was born from an enucleated oocyte!
Chromosomes
Chromosomes are packaged forms of DNA
inside the nucleus.
Chromosomes are not visible in the cells
nucleusnot even under a microscopewhen
the cell is not dividing.
Most knowledge of chromosomes comes from
observations of DNA during cell division.
The haploid human genome contains approximately 3 billion base pairs of DNA
packaged into 23 chromosomes.
Chromosomes
Each chromosome has a constriction point
called the centromere, which divides the
chromosome into two sections, or arms.
The short arm of the chromosome is labeled
the p arm. The long arm of the
chromosome is labeled the q arm.
The location of the centromere on each
chromosome gives the chromosome its
characteristic shape, and can be used to help
describe the location of specific genes.
Chromosomes
Histone proteins are involved in packaging chromosomal DNA into the
microscopic space of the eukaryotic nucleus.
The histone-DNA complex is known as chromatin.
Histones are a family of small, positively charged proteins termed H1, H2A,
H2B, H3, and H4. DNA is negatively charged, and thus binds to histones tightly.
The basic repeating structural (and functional) unit of chromatin is the
nucleosome, which contains eight histone proteins and about 146 base pairs of
DNA
Chromosomes
Histone proteins are not present in most prokaryotes.
Prokaryotes package their DNA by supercoiling.
Multiple proteins act together to fold and condense prokaryotic DNA. In
particular, one protein called HU, which is the most abundant protein in the
nucleoid, works with an enzyme called topoisomerase I to bind DNA and
introduce sharp bends in the chromosome, generating the tension necessary for
negative supercoiling.
Once the prokaryotic genome has been condensed, DNA topoisomerase I, DNA
gyrase, and other proteins help maintain the supercoils.