Cell and molec membrane enclosed organelles

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signal recognition particle
What does SRP stand for?
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ER signal sequence, ribosome
SRP binds to exposed __________ and __________.
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SRP
causes the slowing of protein synthesis (translation) done by the ribosome
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protein translocator
SRP-ribosome complex then binds to a SRP receptor in the ER membrane, and the SRP is released and the ribosome passes from the SRP receptor to a_______________ in the ER membrane. Protein synthesis then resumes and the translocator starts to transfer the growing polypeptide across the lipid bilayer
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What happens when SRP dissociates from the ER signal sequence and the ribosome?
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SRP binding
initiates targeting of ribosomes synthesizing inner-membrane proteins to the translocation pore of the membrane
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the SRP arrests protein synthesis to prevent protein synthesis being finished before targeting is complete and is responsible for targeting signal peptide-bearing proteins to be transported to the ER for secretion or to be used in the plasma membrane
Why is the SRP so important?
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ER
makes up more than half of the membrane of an average cell
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ER
consists of tubules and flattened sacs that extend throughout the cytosol (inside the membrane)
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interconnecting the ER
Tubules are responsible for _______________
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single internal space
The ER lumen is a __________
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ER lumen
an extensive network of membrane tubules, vesicles and flattened cisternae (sac-like structures)
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Making lipids for the mitochondria, peroxisomes, and membranes.
What are the main roles of the ER?
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ER
What makes transmembrane proteins and sequesters Ca++ from the cytosol?
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co-translational translocation
proteins are imported prior to the polypeptide chain being completed
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ER
ribosomes that synthesize proteins are attached directly to the _________
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ribosomes
What coats the surface of the ER?
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post-translational translocation
import proteins to other organelles or ER after synthesis of polypeptide chain is complete
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glycosylation, phosphorylation, and proteolysis
What are examples of post-translational modifications?
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smooth ER
transport vesicles to the Golgi, contain hepatocytes, and holds the enzymes that are required to make cholesterol
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to make lipids, steroid hormones, and detoxify harmful metabolic byproducts. It also acts as a storage facility for Ca++ within the cell.
What are the functions of the smooth ER?
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cytosol
Calcium is released into the ________ and the calcium pump then takes it up
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ER lumen
Calcium pump transports Ca++ from the cytosol into the _____________.
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because the ER serves as a reservoir for fast and specific calcium release
Why does the ER need calcium?
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Ca++
Some parts of the ER are designated for ________ only.
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sarcoplasmic reticulum
muscle cells that are type of modified ER for Ca++ storage
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myofibril contraction and relaxation
the release and uptake of Ca++ is triggered by ______________.
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to produce muscle contractions and relaxation
What is the function of myofibril?
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transmembrane proteins and water soluble proteins
what are the two types of proteins that go to the ER?
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transmembrane proteins are embedded in the lipid bilayer and water soluble proteins are located in the ER lumen
What is the difference between transmembrane proteins and water soluble proteins?
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both have ER signal sequence and both can stay in the ER or be transported
What do transmembrane proteins and water soluble proteins have in common?
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SRP
goes back and forth between the ER and the cytosol and binds to the signal sequence in the ER
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SRP receptor
in the ER membrane and it is able to recognize SRP
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SRP
___________ binds to the ER signal sequence and the ribosome.
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ribosome
SRP causes a pause in translation, so that the ___________ can bind before the polypeptide chain is completed and released into the cytosol.
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SRP-ribosome
bound by ER signal sequence and binds to the SRP receptor protein translocator
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translocator
SRP/ SRP receptor released from the ribosome, but the ribosome remains bound to the ___________ and the translocator will then insert the polypeptide chain into the membrane
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Translocon or translocator
acts as a channel through the hydrophobic membrane of the ER after the SRP has dissociated and translation is continued.
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translocon or translocator
The emerging polypeptide is threaded through the channel as an unfolded string of amino acids by the _________.
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in the ER
Where is the translocon or translocator located in the cell?
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ER membrane bound ribosomes and free ribosomes
What are the two populations of ribosomes?
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they differ in the proteins that they make
How are the two populations of ribosomes different?
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Membrane-bound ribosomes or ER bound organelles
are attached to the cytosolic side of the ER membrane and are engaged in the synthesis of proteins that are being concurrently translocated into the ER
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Free ribosomes
are unattached to any membrane and synthesize all other proteins encoded by the nuclear genome
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ER lumen
Proteins fold and assemble in the _______________, some of them stay in the ER whereas others leave the ER.
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they contain an ER retention signal with 4 amino acids at the C-terminus
What are ER resident proteins?
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they make sure proteins function properly to help other proteins fold and assemble correctly
What is the main function of ER resident proteins?
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protein disulfide isomerase
What is one example of an ER resident protein?
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What does protein disulfide isomerase do?
it catalyzes disulfide bonds
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ER translocator
polypeptide chain can pass through this aqueous channel with a translocon or translocator bound to it
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sec61 complex
a 4 subunit complex that makes up the translocator and generates gated channel
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because if it wasn't a gated channel, all of the Ca++ would leak out
Why is it important that the sec61 complex is a gated channel?
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a translocator and accessory components
What does a translocon consist of?
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polypeptides (it travels from the ribosome to the ER to complete protein synthesis)
What can perform co-translational or posttranslational delivery?
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post-translational translocation
_____________ feeds in the polypeptide into the ER.
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accessory proteins
What does a translocator require to feed the polypeptide chain into the ER?
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ATP hydrolysis (where you break down ATP into ADP)
Therefore, what has to happen for this feeding of the polypeptide chain into the ER to occur?
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ER
During each round of hydrolysis, the translocator pushes a portion of the polypeptide chain into the _________.
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BIP
accessory protein required to function with the translocator
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BIP
plays a major role in chaperoning newly synthesized proteins, and is responsible for maintaining the permeability barrier of the ER during protein translocation, targeting misfolded proteins for retrograde translocation so they can be degraded by the proteasome, contributing to ER calcium stores, and sensing stress in the ER to activate the unfolded protein response (UPR).
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ATP dependent
__________ cycles of BIP binding releases and drives unidirectional translocation
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peroxisomes
a single membrane organelle that does not contain DNA or ribosomes
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in the nucleus
What are all of the proteins encoded for the peroxisome?
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peroxisomes
contains oxidative enzymes that remove hydrogen atoms from organic substrates, therefore making them less acidic and harmful
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hydrogen peroxide
the oxidation reaction that takes place in the peroxisomes produces ______________.
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catalyze
uses H2O2 generated by this reaction to oxidize other substrates
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Peroxisomes
oxidize substrates to detoxify harmful molecules that enter the bloodstream
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liver and kidney cells
Where can peroxisomes be found in your body?
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peroxisomes
can convert excess H2O2 into H2O
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to breakdown fatty acids
What is the major function of peroxisomes?
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2 carbons
Peroxisomes shortens alkyl fatty acids ________ at a time?
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Actetyl CoA
Fatty acids are converted into what?
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plasmalogens
Peroxisomes catalyze the first set of reactions that generate _______________.
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plays a crucial role as endogenous antioxidants that protecting other phospholipids, lipids and lipoprotein particles from oxidative stress
What is the main function of a plasmalogen?
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myelin
Plasmalogens are the most abundant class of phospholipids in ____________.
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neuological disorders like Lorenzo's Oil
What do peroxisome disorders often lead to?
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Where do proteins enter the peroxisomes from?
cytosol and the ER
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peroxins
assist in the formation of peroxisomes by producing the membrane that separates the peroxisome from the rest of the cell and by importing enzymes into the peroxisome
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peroxin
soluble receptor protein in peroxisomes that recognize amino acid signal sequence
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What is the amino acid sequence that peroxins recognize?
Ser-Lys-Leu at the C-terminus
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ATP hydrolysis
What do peroxins require to work?
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peroxins
complex of 6 subunits that form a protein translocator in the peroxisome membrane
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pore
peroxins form a ________, so that proteins have to unfold to enter the membrane.
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delivered via ER-derived vesicles or translocated post-translationally straight from the cytosol
peroxisome proteins are either ....
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outer membrane of the mitochondria
transport into the mitochondria that involves the membrane being in contact with the cytosol
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inner membrane of the mitochondria
encloses the mitochondrial matrix space that forms extensive invaginations
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cristae
What are these extensive invaginations called?
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matrix
the inside compartment of the inner membrane
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intermembrane space
the space between the outer and inner membrane and is continuous with the cristae space
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DNA and ribosomes
the mitochondria has its own _______ and ________.
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they need to unfold
Why do proteins need to do to enter the mitochondria?
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TOM complex
transfers proteins across the outer membrane of the mitochondria
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SAM complex
helps proteins fold properly
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TIM complex
has two complexes (TIM23 and TIM 22) that act as receptors and components of channels
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TIM 22
transport soluble proteins into the matrix space and insert them into the inner membrane
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TIM 23
mediates the insertion of thesubclass of inner membrane proteins and assists them in transport of ADP, ATP, and phosphates in and out of the mitochondria.
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OTA complex
mediates insertion of the inner membrane proteins that are synthesized within the mitochondria
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No
Do prokaryotes have membrane-bound organelles?
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What is the cell membrane system composed of?
nucleus, ER, Golgi and plasma membrane
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DNA and ribosomes
Mitochondria and chloroplasts have their own ___________ and ______________.