Proteins are made up of
Amino Acids
How many types of amino acids are there?
20 amino acids
Amino acids are made up of 4 main things:
A carbon atom bonded to H
An amino group
A carboxyl group
An R group
1° primary structure of a protein
Amino acid sequence
2° secondary structure of a protein
Spirals or folds
3° tertiary structure of a protein
Complex 3-D shape that gives protein its function
4° quaternary structure of a protein
Some proteins need more than one piece to make the final protein
Enzyme
A type of protein that speeds up the rate of chemical reactions
Steps of how an enzyme works
Bring substrates together in a precise orientation at the active site
Binding to the active site
Destabilizes bonds in the substrates, allowing new bonds to form
R-groups that line the active site form temporary covalent bonds that assist with transfer of atoms from one reactant to another
A final product is formed and released
Induced Fit
The substrate induces a slight change in the shape of the enzyme that it can fit perfectly
Competitive inhibition
Occurs when a regulatory molecule directly blocks the active site
Blocks the active site so that the substrate can’t bind
Allosteric regulation
Occurs when a regulatory molecule binds somewhere other than the active site
Changes the shape of the enzyme so that the substrate can’t bind
How to reverse competitive inhibition
An increase in the substrate concentration can return enzyme activity to 100%
How to reverse allosteric inhibition
An increase in the substrate concentration can increase enzyme activity but it will not reach 100% unless there is no longer a regulatory molecule present
Metabolic pathway
A specific molecule is altered in a series of steps that results in a final product
Inside a cell what are 3 jobs of proteins
Enzymes facilitate chemical reactions inside the cell.
Cytoskeleton (microfilament protein) gives the cell its shape.
Microtubules facilitate chromosome movement during cellular division.
Between cells what are 3 jobs of proteins
Insulin relays a message to other cells.
The Na/K pump transports sodium out of the cell and potassium into the cell.
Hemoglobin carries oxygen to cells all over the body.
Primary structures of all proteins are manufactured by
ribosomes
Signal sequence
either the first few amino acids, or the last few amino acids in the chain
Chemical label
A chemical group added to a protein after it’s completely finished being manufactured, folded, and specialized
Endoplasmic Reticulum
formed from invaginations of the nuclear envelop
Proteins travel through __ and then bud off in __
Proteins travel through RER and then bud off in VESICLES
Vesicles fuse to the _
Golgi Apparatus
Proteins leave GA for the _ or bud of GA in _
Proteins leave GA for the CELL MEMBRANE or bud of GA in VESICLES
When proteins bud off GA in vesicles that become _
lysosomes
The endomembrane system_
The endomembrane system folds, specializes, packages, transports and receives (lipids and) proteins which have an ER signal sequence
Steps of Protein manufacture, specialization, packaging, transporting and receiving in the endomembrane system
A ribosome begins protein manufacture (in the cytoplasm)
The first few amino acids serve as the ER signal
The ER signal sequence binds to the signal recognition particle which pauses translation
The SRP binds to a receptor on the rough endoplasmic reticulum
The amino acid chain is threaded through the receptor into the RER
SRP detaches. Ribosome completes the primary structure . The amino acid chain is released
What happens in the RER (4 things)
After the SRP leaves, the ribosome completes the primary structure while its attached to the RER membrane
Once primary structure is completed the amino acid chain is released into the interior (lumen) of the RER
Proteins are folded inside the RER
Enzymes produce glycoproteins
Glycoproteins
Proteins with added carbohydrate side chains
What happens in the GA? (8 things)
Proteins bud off in vesicles composed of the ER membrane.
They fuse to the cis side (closest to the nucleus). Proteins flow inside.
Proteins are moved along the \n membranes of the GA, encountering different groups of enzymes at each step.
Proteins are modified and specialized by enzymes encountered in each cisternae (membrane section).
Many receive chemical labels.
Once proteins reach the trans side those with chemical labels bud off in vesicles.
Vesicles carrying lysosome proteins develop into lysosomes
Proteins without chemical labels are released from the GA and travel to the cell membrane
What happens in the lysosome? (3 things)
Vesicles that have budded off from the GA and are carrying lysosome proteins develop into lysosomes
Lysosomes digest foreign materials that have been brought into the cell.
The resulting macromolecules are recycled to make new materials.
The Cell Theory
All life is composed of one or more cells...the cell is the basic unit of life. \n All cells arose from other cells
Prokaryote
Unicellular organisms (bacteria, archaea)
No membrane bound organelles Contain ribosomes
Non-membrane bound nucleoid
Does not have mitochondria
DNA is circular and can be arranged in one chromosome
Small size
Some have flagellum which helps it move
Some have fimbriae which help it attach
Eukaryote
Multicellular organisms (animals, plants, fungi, protists)
Membrane bound organelles in cell (ER, GA, lysomes)
Membrane bound nucleus
Mitochondria/chloroplast
DNA is linear and arranges in multiple chromosomes
Large size
Desmosomes (animals) and plasmodesmata (plants)
How are prokaryotes and eukaryotes related?
Eukaryotes and Archaea share more distinct features suggesting they inherited them from a recent common ancestor
The Theory of Endosymbiosis
A bacteria got inside of an archaea cell and that bacteria evolved into the mitochondria and chloroplast
Development of The Theory of Endosymbiosis
First proposed in 1905 but was ignored for several decades
In 1967 Lynn Margulis published a paper about it and was net with intense criticism
Her idea that cooperation (between the proto-eukaryote and engulfed prokaryote) could be a driving force of evolution was counter to the prevailing ideas of the time that only competition was important.
Regardless of the opposition, evidence for her hypothesis began to mount
Are prokaryotic cells compartmentalized?
No
Meaning that there are no organelles. \n Everything is just floating around inside the cell without any separation
Are eukaryotic cells compartmentalized?
Yes
Meaning that there are organelles.
Most things are separated from each other
Cell Attachment
Molecules that attach one cell to another are often proteins that span \n the cell membrane and extracellular matrix.
Cells attach to each other temporarily to perform a function or attach \n semi-permanently to form a tissue
The extracellular matrix (of animal cell)
Surrounds the outside of the cell membrane
Composition of extracellular matrix is unique to cell type
Composition of the extracellular matrix (of animal cell)
Proteoglycans-proteins with lots of cards attached. Protects cell
Collagen-rope-like protein. Provides strength and form
Integrins-span the cell membrane. Connects the inside of the cell to the ECM
Specifics of the composition unique to the cell type
Cell Communication
A signal sent from one cell has to recognize and bind to the correct receiving cell
Signals (hormone or neurotransmitter) can be proteins or other molecules
Receptors are proteins that are on or inside the cell membrane of receiving cells
The signal will fit perfectly into the receptor
Neurotransmitters
Travel through nerve cells in the nervous system to reach their destination.
Fast response
Hormone
Travel in blood to reach their destination
Slow response
Nucleic aicids consist of
nucleotides
Nucleotides are…
polar
Nucleotides are composed of (3 things)
Phosphate group
Nitrogenous base
Sugar: deoxyribose in DNA and ribose in RNA
RNA
Sugar is ribose
Single stranded96
DNA
Sugar is deoxyribose
Double Stranded
Double helix
RNA is __ reactive than DNA
RNA is MORE reactive than DNA
DNA sequence
the order of nucletides
dictates the order of amino acids for the resulting protein
5’ end
phosphate attached to the 5’ carbon on the sugar
3’ end
3’ carbon on the sugar
Antiparallel
2 nucleotides are arranged opposite in orientation to each other
When 2 nucleotides are bonded
Mitosis
Cell replication to create identical cells
One cell divides into 2 diploid daughter cells
dealing with a nuclear membrane & multiple chromosomes require mitosis to have more steps than binary fission
Meiosis
Cell replication to create haploid gamete
One cell divides into 2 daughter cells and then the 2 daughter cells each divide
The result is 4 haploid daughter cells
Replication bubble
forms during DNA synthesis
Replication fork
Y-shaped region where the parental strands are separated
where active DNA synthesis takes place
Steps of DNA replication
DNA helicase breaks the hydrogen bonds between the nucleotides in that location & opens the double helix so that the two strands separate at the replication fork. \n The unwinding of DNA strands should create twists further down the helix, but \n topoisomerase binds to relieve twisting forces.
Single-strand DNA-binding proteins attach to the separated strands to prevent them from snapping back into a double helix
Primase lays down primer on both strands
An RNA strand about 10 ribonucleotides long
Forms complementary base pairs with the DNA template strand
DNA polymerase α or ε synthesizes the leading strand by attaching nucleotides to the 3’ OH ends of the primer and extending it
DNA polymerase δ synthesizes the lagging strand and replaces primers with \n deoxyribonucleotides
DNA helicase
breaks the hydrogen bonds between the nucleotides in that location & opens the double helix so that the two strands separate at the replication fork
Topoisomerase
binds to relieve twisting forces
Leading strand
strand that is synthesized towards the fork
synthesis is straightforward
Lagging strand
strand that is synthesized away from the fork
causes gaps in synthesis
Direction of synthesis
3’ to 5’ on template strand
5’ to 3’ on daughter strand
Primase
lays down primer on both strands
Why primase adding primer is necessary
DNA polymerase can only \n add nucleotides to a free OH \n group, it can only extend a \n pre-existing strand... but when DNA strands are separated there are no free OH groups
Primase provides the free 3’ OH \n group that DNA polymerase \n needs to start adding nucleotides
DNA polymerase α or ε
synthesizes the leading strand by attaching nucleotides to the 3’ OH ends of the primer and extending it
DNA polymerase δ
synthesizes the lagging strand and replaces primers with deoxyribonucleotides
Ligase
seals the gaps between the Okazaki Fragments
endonuclease
Removes the RNA when DNA pol δ gets to the end of its new \n daughter strand and bumps up against the older daughter strand, thus dislodging the old primer
Okazaki Fragments
Fragments of new daughter \n DNA
Lagging strand
Proofreading
Fixes mistakes in DNA synthesis.
DNA polymerase fixes its own mistakes
A newly added base that is not paired correctly creates misalignment.
DNA polymerase’s active site can identify misalignment. Once detected, DNA polymerase will pause.
DNA polymerase has exonuclease activity – it will remove the mismatched nucleotide. Then replace it with the correct one.
Mismatch Repair
Fixes mistakes in DNA synthesis not repaired by proofreading
A mismatch is detected \n immediately after DNA synthesis is finished.
Proteins and enzymes cut out the mismatch
DNA polymerase returns to add the correct nucleotides.
DNA ligase seals the breaks.
Nucleotide excision repair
Fixes DNA damaged by UV light
UV light from the sun or tanning beds can cause a covalent bond to form between adjacent pyrimidine bases within the same strand. This causes a kink.
Protein complexes detect the \n kink, remove the section of DNA containing the kink.
DNA polymerase adds in the \n nucleotides and ligase seals the breaks.
Binary Fission
Cellular cloning
asexual reproduction by a separation of the body into two new bodies
Cell Cycle
Interphase (G1, S, G2)
Mitosis (PMAT)
Cytokinesis
PMAT
Prophase (DNA condenses into chromosome)
Prometaphase (The nuclear envelope disintegrates)
Metaphase (The chromosomes are lined up in middle)
Anaphase (Sister chromatids pulled apart)
Telophase (2 nuclei form)
G1
DNA is uncondensed (chromatin). The cell is fulfilling its function. It is \n “deciding” to replicate (longest phase)
S phase
DNA replicates
G2 phase
The cell grows to prepare for M phase
Sister Chromatids
Homologous chromosome and identical copy
Made through replication
Homologous Chromosomes
A chromosome pair
Prophase
DNA condenses into compact chromosomes
The spindle apparatus forms - produces mechanical forces that move replicated chromosomes during early mitosis and pull sister chromatids apart in late mitosis. It is composed of microtubule proteins.
Prometaphase
The nuclear envelope disintegrates.
Kinesin and dynein motor proteins attach to the kinetochores at the centromere and walk the chromosomes up and down the microtubules, until they reach the middle of the spindle.
Metaphase
The chromosomes are lined up at the metaphase plate. \n The microtubules overlap in the middle of the cell creating a pole-to-pole connection
Anaphase
The cohesion that holds sister chromatids together splits.
Sister chromatids are pulled apart by the depolymerization of the \n microtubules.
Because sister chromatids are pulled apart, homologous \n chromosomes end up together in the new cells.
The two poles of the spindle are pushed and pulled farther apart by specialized proteins.
Telophase
The spindle microtubules are fully depolymerized to remove the spindle. Sister chromatids reach the opposite poles. \n The nuclear envelope re-forms around each set of chromosomes. \n Once two independent nuclei have formed, mitosis is complete.
Cytokinesis
Cytoplasm is divided equally between the two new cell regions.
Then, cytoskeletal fibers form the contractile ring which pinches the cell into two new cells
G1 Checkpoint
Cell size is adequate
Nutrients are sufficient
Social signals are present
DNA is undamaged
G2 Checkpoint
Chromosomes have replicated successfully
DNA is undamaged
Activated MPF is present
M-phase checkpoints
chromosomes have attached to spindle apparatus
chromosomes have properly segregated and MPF is absent
Regulator molecule
active at checkpoints
prevent the division of cells that are damaged or are in poor condition
Apoptosis
Programed death of cell (dignified)
Cyclins
work by binding enzymes called cyclin dependent kinases
prompt the movement of cells from one phase to the next
When cyclin binds to Cdk
Cyclin activates Cdk
Guides it to a specific set of proteins for phosphorylation.
M phase promoting factor
Composed of Cdk and M cyclin.
When the concentration of M cyclin is high enough it causes the formation of MPF.
Then, the kinase subunit catalyzes the phosphorylation of other proteins to start M phase.
Anaphase-promoting \n complex/cyclosome
MPF activates APC/C during anaphase.
APC/C adds a small protein tag, ubiquitin, to its targets.
Molecules tagged with ubiquitin get destroyed.
Thus, APC/C destroys proteins, stopping their function