Ch3 CELL
Ch3 CELL
of Organization
LEARNING OUTCOMES
Integral
membrane
proteins are
embedded in
membranes
(amphipathic).
Peripheral May extend all
proteins are on the the way through
surface of cell (transmembrane)
membranes.
PROTEINS OF THE CELL MEMBRANE
Proteins determine most of the membrane’s specific functions.
SIX major functions performed by membrane proteins:
1. Enzymes (catalyzes intracellular or extracellular reaction)
2. Transport (ion channel or transporter)
3. Receptors for signaling molecules
4. Cell-cell recognition
5. Intercellular junctions
CARBOHYDRATES OF THE PLASMA MEMBRANE
Carbohydrates are found on the glycocalyx (calyx = “husk” or “pod”), an
extensive “sugary” coat on the outer surface of the cell membrane
The glycocalyx functions in cell
recognition, cell signaling, cell-cell
adhesion, cell protection, and increases
moisture around the cell (glycocalyx
attracts water)
Carbohydrates attach to some proteins
(forming glycoproteins) and lipids (forming
glycolipids)
MEMBRANE PERMEABILITY
50 50
40 40
30 30
20 20
10 10
0 0
left right left right
Under diffusion, will solutes move down/with (from high to low concentration) or
up/against (from low to high concentration) their concentration gradient?
PRINCIPLE OF DIFFUSION
Diffusion is the movement of solutes from an area of high solute concentration
to an area of low solute concentration;
Each substance moves down its own concentration gradient independently of
other solutes
FACTORS AFFECTING DIFFUSION RATE
The rate (speed) of diffusion will be affected by:
1. Steepness of the concentration gradient (faster when gradient is steeper)
2. Temperature (faster when warmer)
3. Mass of diffusing particle (faster when smaller)
4. Surface area of membrane doing the diffusion (faster when larger)
5. Distance over which diffusion must occur (faster when small/when the
two areas are closer to one another)
These factors will be important when we discuss respiration later on!
FACILITATED DIFFUSION USES TRANSPORT
PROTEINS
These proteins span the membrane and allow
diffusion across the membrane of solutes that are
too polar or highly charged
Each transport protein is specific to one or a few
closely related solutes.
Some are channels (for diffusion of ions) and
others are carriers (for diffusion of glucose,
fructose, galactose and some vitamins)
The number of channels or carriers present affect
rates of facilitated diffusion
ACTIVE TRANSPORT
End point of diffusion: 50/50 split of particles on either side of the membrane
50
across a membrane against their
40
concentration gradients?
30
20
ACTIVE TRANSPORT
10
0
left right Requires energy
Active transport can be powered directly via ATP → primary transport
Active transport can be powered via harnessing the flow of another solute down
its concentration gradient → secondary transport
PRIMARY ACTIVE TRANSPORT
ATP is hydrolysed to ADP + P, causing a carrier protein to change shape
EXAMPLE: THE NA+/K+ PUMP
Maintains a low concentration of Na+ inside the cell (pumps Na+ out) and a
high concentration of K+ inside the cell (pumps K+ in) → ‘salty banana’
Uses 40% of cellular ATP (65% in neurons)
Operates continually
SECONDARY ACTIVE TRANSPORT (CO-TRANSPORT)
A form of active transport that involves energy, but does not DIRECTLY
involve ATP → ATP is used INDIRECTLY
One solute flowing down its
concentration gradient (usually Na+) is
used to drag in or push out a second
solute against its concentration gradient
Symporters are molecules that
move two solutes in the same direction
Antiporters are molecules that
move two solutes in opposite directions
PASSIVE VS. ACTIVE TRANSPORT
Passive transport
Includes diffusion AND facilitated diffusion
▪ Does NOT require energy
▪ Solutes move down their concentration gradient
▪ May or may not require a membrane protein
Active transport
▪ Requires energy
▪ Solutes are pumped against their concentration
gradient
▪ Requires a membrane protein
TRANSPORT OF MOLECULES IN VESICLES
Functions:
1. Establishes and maintains cell shape
2. Provides mechanical strength
3. Locomotion
4. Chromosome separation during cell
division
5. Intracellular transport of organelles
CYTOSKELETON
The cytoskeleton is
comprised of 3 types
of fibers:
1. Microfilaments,
2. Intermediate
filaments,
3. Microtubules
MICROFILAMENTS
Composed of double-twisted filaments of actin and
myosin
▪ Help generate movement
▪ Muscle contraction
▪ Cell division
▪ Cell locomotion
▪ Found in microvilli
Compare
and contrast
cilia and
flagella
CENTROSOME/CENTRIOLES
The centrosome is a microtubule
organizing centre
▪ Consists of a pair of centrioles
and pericentriolar matrix
All the cells in your body contain the same 46 chromosomes and therefore, the same
genes
However, different cell types have unique structures and functions
How can this be if they all have the same genes?
Different sets of genes are turned on or off in different cells
▪ If a gene is turned on → transcribed into mRNA → translated into protein
▪ If a gene is turned off → no mRNA transcribed → no protein produced
CENTRAL DOGMA = PROTEINS ARE PRODUCED FROM DNA
Protein synthesis is a 2 step event:
DNA Protein
1 2
Transcription Translation
in Nucleus in Cytoplasm
TRANSCRIPTION OF DNA TO RNA
Genetic information encoded in DNA is copied
onto a strand of RNA
1. RNA polymerase binds to the promoter
▪ RNA polymerase is an enzyme that makes an
RNA polymer
2. RNA nucleotides are added complementary to
one strand of DNA
▪ DNA molecule is ‘unzipped’
▪ RNA nucleotides that fit with the DNA are
added one at a time
3. RNA polymerase detaches at the
terminator sequence
RNA EDITING/ SPLICING
There are segments of the RNA transcript that will be
cut out (introns) and segments that are destined to be
turned into amino acid sequence (exons)
4. Introns in pre-mRNA are cut out (RNA splicing)
5. Exons are pasted together and form the mRNA -
code for the protein
RNA transcript can be spliced many different ways
(introns sometimes left in) which results in different
proteins (how we can have 10000 genes but millions of
different proteins)
TRANSLATION
The mRNA strand is read by a ribosome,
which then assembles the appropriate amino
acids into a protein
THE GENETIC CODE
The sequence of nucleotides determines
the sequence of amino acids along a
polypeptide chain.
MITOSIS MEIOSIS
Somatic cell division → When body ▪ Reproductive cell division →
cells divide and 1 cell splits into 2 cells Production of gametes (eggs and
▪ Results in an increase in the number of sperm)
body cells ▪ Parents cells have 2 sets of 23
▪ Produces 2 daughter cells that are chromosomes (diploid); each
identical to the parent cell daughter cell has one set of 23
▪ Nuclear division = mitosis chromosomes (haploid)
▪ Cytoplasmic division = cytokinesis ▪ Nuclear division = meiosis (2
successive nuclear divisions)
▪ Cytoplasmic division = cytokinesis
SOMATIC CELL CYCLE
The somatic cell cycle
consists of interphase and
the mitotic phase (cell
division)
SOMATIC CELL CYCLE:
INTERPHASE
Interphase (G1, S, G2)
▪ Vast majority of a cell’s life
▪ All processes occur except cell division
Centromeres line up at
the exact center of the
mitotic spindle
(metaphase plate or
equatorial plane)
46 chromosomes
lined up (92
chromatids in
total)
MITOSIS: ANAPHASE
Separation of sister
chromatids at their
centromeres
Movement of the two
sister chromatids
toward opposite
poles of the cell
MITOSIS: TELOPHASE
Presence of a cleavage furrow
Chromosomes uncoil and revert to
chromatin
Nuclear envelope reforms
CYTOPLASMIC DIVISION
Cytokinesis: Division of
cytoplasm and organelles.
The process begins in late
anaphase or early telophase
with the formation of a
cleavage furrow.
MITOSIS
Your challenge: a
memorable memory
aid to remember these
stages
LEARNING OUTCOMES
23 PAIRS of
chromosomes
lined up
MEIOSIS I – ANAPHASE I AND TELOPHASE I
Anaphase I: the members of each homologous pair separate, with one
member of each pair moving to an opposite pole of the cell.
Telophase I and cytokinesis: similar to telophase and cytokinesis of mitosis.
Each resulting cell is haploid; contains only 23 chromosomes – one of each starting pair.
MEIOSIS II
Meiosis II consists of prophase II,
metaphase II, anaphase II, and
telophase II