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ER, Golgi, Peroxisomes, Endosomes, Lysosomes, Signal Transduction

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Answer
Which of the following is incorrectly matched: A. rough ER and protein synthesis B. terminal glycosylation and Golgi C. Ca storage and smooth ER D. secretory vesicle shipping and cis-Golgi network E. transitional vesicle formation and rough ER   D. secretory vesicle shipping and cis-Golgi network  
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What makes up the endomembrane system?   ER, Golgi, lysosomes, and endosomes  
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Which of the following is not part of the endomembrane system: A. ER B. endosomes C. lysosomes D. peroxisomes E. Golgi   D. peroxisomes  
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A protein can be glycosylated and translated at the same time.   True  
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Flippases aid in attaching oligosaccharides to proteins.   False  
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Calreticulin binds to improperly folded proteins and targets them for degredation.   False  
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Transfer of oligosaccharides to proteins always occurs in ER lumen.   False  
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In receptor-mediated endocytosis, dynamin inhibition would prevent vesicle formation.   True  
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In receptor-mediated endocytosis, coated pits would form in the absence of adapter proteins as long as clathrin was present.   False  
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In receptor-mediated endocytosis, a coated vesicle can fuse with endosomes.   False  
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In receptor-mediated endocytosis, a ligand can bind to any receptor as long as it's on the cell surface.   False  
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Which of the following is not part of the vesicle-sorting pathway: A. v-SNARE B. Golgin C. m-SNARE D. Rab GTPase E. Syntaxin   C. m-SNARE  
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Syntaxin   type of v-SNARE  
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Golgin   type of tethering protein  
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Labeled protein seen only in ER   protein contains RXR (Arg-X-Arg) retention tag  
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Anterograde pathway through endomembrane system   rough ER -> cis-Golgi network -> trans-Golgi network -> plasma membrane  
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The smooth ER is enriched in glycogen-6-phosphatase which helps break down glycogen.   False--glucose-6-phosphatase  
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What is the oligosaccharide carrier in glycosylation called?   dolichol phosphate  
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Zymogen granules are part of constitutive secretory pathway.   False  
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GTP-bound SarI recruits and binds COP I proteins for vesicle coat formation.   False--SarI goes with COP II, COP I goes with ARF  
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Step #1 of lysosomal protein targeting   N-glycosylation  
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Step #2 of lysosomal protein targeting   transition vesicle formation  
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Step #3 of lysosomal protein targeting   mannose phosphorylation  
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Step #4 of lysosomal protein targeting   receptor binding  
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Step #5 of lysosomal protein targeting   increase in lumen [H+]  
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The continuous secretion of mucus from epithelial cells in your intestines is an example of what type of exocytosis?   constitutive/continuous secretion/exocytosis  
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Where are glycosyl transferases found?   in Golgi  
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What do glycosyl transferases do?   transfer oligosaccharides to glycoproteins (goes with glucan synthatase)  
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Which is needed for synthesis of proteins in ER: A. KDEL tag B. cytosolic ribosome C. SRP D. cytosolic ribosome and KDEL tag E. SRP and cytosolic ribosome   E. SRP and cytosolic ribosome  
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Functions of the ER   "production line": protein synthesis, lipid synthesis, and membrane synthesis  
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Transitional elements (TEs)   help transport "packages" from ER to Golgi  
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_______ is recruited by an ER signal sequence on a cytoplasmic ribosome, and then binds to rough ER so protein synthesis can continue.   SRP  
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Step #1 of protein modification and degredation   glycosylation produces glycoproteins  
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glycosylation   the attachment of carbohydrate chains to proteins  
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glycoproteins   proteins with carbohydrate chains  
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Step #2 of protein modification and degredation   protein folding and assembly  
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Step #3 of protein modification and degredation   ER-associated degredation (ERAD)  
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ER-associated degredation (ERAD)   improperly folded proteins are exported for degredation  
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hydroxylation   OH groups are added to make drugs/toxins more soluble (less toxic)  
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monooxygenase   in cytochrome P-450, the enzyme involved in hydroxylation  
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aryl hydrocarbon hydroxylases   in cyt P-450, the enzymes that targets polycyclic hydrocarbons  
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Carbohydrate metabolism in smooth ER Step #1   glucose stored as glycogen (glucose polymer)  
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Carbohydrate metabolism in smooth ER Step #2   glycogen is broken down into glucose-1-phosphate  
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Carbohydrate metabolism in smooth ER Step #3   glucose-1-phosphate is made into glucose-6-phosphate  
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Carbohydrate metabolism in smooth ER Step #4   glucose-6-phosphatase removes the phosphates from glucose-6-phosphate to make glucose  
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sarcoplasmic reticulum   smooth ER found in muscle cells involved in muscle contraction/relaxation  
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HMG-CoA reductase   enzyme crucial for cholesterol synthesis target for statin drugs that try to lower cholesterol  
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smooth ER functions   detoxification, carbohydrate metabolism, calcium storage, and biosynthesis of steroids  
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________ and _________ are the main components of membranes   phospholipids and cholesterols  
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What membranes are produced in the ER?   all except mitochondria, chloroplast, and peroxisome membranes  
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phospholipid translocators   flippases, aid in flip-flop/transverse diffusion  
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Cis-Golgi Network (CGN)   faces ER, "recieving"  
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Golgi medial cisternae   middle, contains lumen, "sorting and processing"  
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Trans-Golgi Network (TGN)   opposite side of CGN, "shipping"  
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Golgi Stationary Cisternae Model   each compartment of the Golgi is stationary, and shuttle vesicles transport between cis and trans  
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Golgi Cisternae Maturation Model   compartments of the Golgi are transient and dynamic  
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anterograde transport   ER -> Golgi -> plasma membrane  
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retrograde transport   plasma membrane -> Golgi -> ER  
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Where does protein glycosylation occur?   ER and Golgi  
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N-glycosylation   linkage of sugar molecules  
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O-glycosylation   attachment of carbohydrates to molecules  
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Where does glycosylation begin?   ER membrane  
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glycosylation in ER membrane step #1   biosynthesis and processing of carbohydrate chains  
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glycosylation in ER membrane step #2   identification and removal of misfolded proteins  
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glycosylation in ER membrane step #3   attachment of carbohydrate chain to protein  
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glycosylation in Golgi step #1   addition or removal of carbohydrate chains  
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dolichol phosphate   olgigosaccharide carrier in ER lumen  
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calnexin (CNX)   membrane-bound protein involved in protein folding  
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calreticulin (CRT)   soluble protein involved in protein folding  
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UDP-glucose glycoprotein transferase (UGGT)   enzyme that binds to improperly folded proteins to signal to CNX or CRT that they need fixed  
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glucan synthetases   enzymes that produce olgiogosaccharides from monosaccharides in the ER  
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glycosyl transferases   enzymes that attach carbohydrate groups to proteins in the ER  
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________are found in localized proteins.   retention tags  
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RXR   retention tag Arg-X-Arg  
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________bind to Golgi receptors and transport a protein back to the ER.   retrieval tags  
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KDEL   retrieval tag Lys-Asp-Glu-Leu  
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KKXX   retrieval tag Lys-Lys-X-X  
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Where are hydrolytic enzymes found?   within lysosomes  
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_______is a type of vacuole that becomes a secretory vesicle.   condensation vacuole (CV)  
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_______are mature secretory vesicles that form from CVs   zymogen granules (ZG)  
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Secretory pathway to plasma membrane   rough ER -> Golgi -> aggregate into CV -> CV becomes ZG as more aggregate -> secretion  
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Constitutive secretion is_______.   continuous  
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In __________ ___________, secretory vesicles accumulate until an extracellular signal is recieved.   regulated secretion  
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Exocytosis is transport ______ cell.   out of  
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Endocytosis is transport _____ cell.   into  
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________-________ is regulated exocytosis that responds to ____ within a cell, and is found in the smooth ER.   calcium-triggered, [Ca]  
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______ ______ is exocytosis at very specific sites in the plasma membrane, and is found in nerve cells.   polarized secretion  
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"cellular eating"/intake of large particles   phagocytosis  
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_____ _____ are indigestible materials left in lysosomes that can be expelled into the cytoplasm, and accumulation of it can determine cellular aging. Macrophages also transport these to the immune system to help the body recognize and fight infections.   residual bodies  
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autophagy   organelle digestin/recycling  
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autophagosome   lysosome used in autophagy  
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macrophagy   autophagy of large organelles  
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What are the causes of lysosomal storage diseases?   the accumulation of polysaccharides or lipids in organs, and/or missing digestive enzymes  
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The accumulation of glycogen in different organs (liver, heart, skeletal muscle) is the cause of ____ ____ ____.   Type II Glycogenosis  
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The accumulation of gangliosides (lipids) in the brain causes ____-____ ____.   Tay-Sachs Disease  
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The accumulation of glycosaminoglyccans in ECM causes ___ ___ ___ ___.   Hurler and Hunter Syndrome  
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peroxisomes   single membrane-bound organelles not derived from ER  
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catalase   enzyme found in peroxisomes that breaks down hydrogen peroxide  
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oxidase   enzyme found in peroxisomes that makes hydrogen peroxide  
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peroxidases   both oxidize and break down hydrogen peroxide  
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reactive oxygen species   hydrogen peroxide, O2-, OH+  
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Beta (B) oxidation   fatty acid oxidation in peroxisomes, and produces acetyl CoA/succinyl CoA for Krebs cycle  
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aminotransferases   move amino groups around on molecules  
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leaf peroxisomes   close to mitochondria and chloroplasts, involved in photorespiration  
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glyoxysomes   convert fats/fatty acids to sugars/sucrose, and are present in fat-storage tissues (endosperm), and they become peroxisomes as plants mature and no longer need the endosperm  
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peroxisome biogenesis   replication of peroxisomes  
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peroxin   trans-membrane protein that helps bring in catalases  
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peroxisome targeting sequence   SKL (Ser-Lys-Len)/PTS-1 found at end of a protein  
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Vm   resting membrane potential, -60 mV for most cells  
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electrical excitability   the response to stimuli resulting in changes in the Vm (action potential), and it is rapid and reversible  
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electroneutrality   in solution, for each ion, A, ther is an equal amount of oppositely charged ions, B  
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current   the movement of the ions  
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electrical potential (voltage)   "opposites attract"  
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selective permeability: Na+/K+ pumps   ion channels control what goes in and out of cell  
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cation channel leakage   some ions go in/out that should not  
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electrochemical equilibrium   forces that pull cations out = forces that pull them in  
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Nerst Equation   shows relationship between ion gradient and equilibrium potential for a selectively permeable membrane, but only considers one ion  
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net charge inside cell   negative  
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net charge outside cell   positive  
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repolarization   K+ flows out of cell (outflux)/Vm becomes more negative  
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depolarization   Nat+ flows into cell (influx)/Vm becomes more positive  
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Goldman Equation   considers all ions and relative permeability  
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multimeric voltage-gated channels   K+ channels made up of 4 proteins  
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monomeric voltage-gated channels   Nat+ channels made up of 1 protein  
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inactivating particle   helps regulate voltage-gated channels  
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voltage sensor   detects signal and tells channel to open or close, S4  
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____-____ ____ uses specific receptors that are found on the outer surface of the plasma membrane.   receptor-mediated endocytosis  
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Step #1 in receptor-mediated endocytosis   ligands bind to receptors on outer surface of plasma membrane  
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coated pits   specialized membrane regions that serve as sites for collection and internalization of receptor-ligand complexes  
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Step #2 in receptor-mediated endocytosis   receptor-ligand complexes encounter coated pits  
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Step #3 in receptor-mediated endocytosis   accumulation of receptor-ligand complexes triggers accumulation of additional proteins (adaptor proteins, clathrin, and dynamin) on cytosolic surface of plasma membrane  
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Step #4 in receptor-mediated endocytosis   invagination of plasma membrane continues until it pinches off and forms a coated vesicle  
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Step #5 in receptor-mediated endocytosis   clathrin coat is released to leave the vesicle uncoated  
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Step #6 in receptor-mediated endocytosis   coat proteins and dynamin are recycled to plasma membrane, and become available for formation of new vesicles while uncoated vesicle is able to fuse with an early endosome  
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desenstitization   EGF receptor internalization leads to the cell becoming less receptive to EGF  
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early endosomes   sites for the sorting and recycling of extra-cellular material brought into the cell by endocytosis  
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ATP-dependent proton pump   found in the endosomal membrane and maintains the lower pH  
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transcytosis   a pathway that takes extracellular material from one side of the cell (endocytosis) to the opposite side (exocytosis)  
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fluid-phase endocytosis   a cltahrin-independent endocytic pathway that takes in extracellular fluid  
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clathrin   coat protein that goes with AP1, AP2, and ARF; vesicles involved in selective transport of proteins from TGN to endosomes and in the endocytosis of receptor-ligand complexes from the plasma membrane  
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COPI   coat protein that goes with ARF; facilitate retrograde transport of proteins from Golgi to ER, Golgi and cisternae  
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COPII   coat protein that goes with Sar I; involved in transport of material from ER to Golgi  
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Caveolae   small invaginations of plasma membrane characterized by protein caveolin; type of lipid raft rich in cholesterol and shipgolipids  
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triskelions   a multimeric protein composed of three large polypeptides and three small polypeptides radiating from a central vertex; component of clathrin coats  
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adapter protein (AP)   component of clathrin coats; ensure that appropriate macromolecules are converted in coated pits, mediate attachment of clathrin to proteins embedded in plasma membrane  
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dynnamin   a cytosolic GTPase required for coated pit constriction and closing of the budding vesicle  
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uncoating ATPase   essential for uncoating mechanism  
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ADP ribosylation factor (ARF)   small GTP-binding protein, mediates COPI protein  
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SNARE hypothesis   the proper sorting and targeting of vesicles in eukaryotic cells involves two families of SNARE/SNAP receptor proteins (v and t-SNARE) found on transport vesicles and target membranes  
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v-SNARE (vesicle-SNAP receptors)   found on transport vesicles, complementary with t-SNARES so that vesicles can recognize and fuse with target membrane  
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t-SNARE (target-SNAP receptors)   found on target membranes, complementary with v-SNARES so that vesicles can recognize and fuse with target membrane  
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Rab GTPases   facilitates membrane fusion by locking complementary t-SNARE and v-SNARE together  
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N-ethylmaleimide-sensitive factor (NSF)   mediates release of v and t-SNARES of donor and target membranes along with SNAPs  
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soluble NSF attachment proteins (SNAPs)   mediate release of v and t-SNARES of donor and target membranes along with NSF  
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tethering proteins   act over longer distances and provide specificity by connecting vesicles to target membranes before v-SNARE/t-SNARE interactions; two main types: coiled-coil proteins, multisubunit complexes  
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golgins   coiled-coil proteins used in initial recognition of COPI or COPII coated vesicles to Golgi  
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What do conserved oligomeric Golgis (COG), Goldi-associated retrograde proteins (GARP), and transport protein particles (TRAPP) have in common?   they are multisubunit tethering complexes implicated in the initial recognition and specificity of vesicle-target membrane interaction  
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inactivating particles   block channel pore so gate will not open until it receives a signal telling it to leave  
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action potential   significant depolarization and repolarization of neuronal plasma membrane  
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threshold potential   the upper limit of Vm that induces the action potential; point where large change in voltage occurs  
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propagation   the transfer of the action potential through nerves  
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resting potential   voltage gates are closed  
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subthreshold depolarization   blips of activity due to leakage that do not cause action potentials because threshold is not reached  
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depolarization phase   cell has increased permeability to Na+  
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depolarization stimulus   takes voltage to threshold and Na+ rushes into the cell  
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repolarization phase   peak membrane potential is reached, and Na+ channels are inactivated while K+ channels open  
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absolute refractory period   no more depolarization occurs  
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hyperpolarization phase   Na+ channels remain inactivated while K+ channels remain open and voltage goes below membrane potential before voltage goes back up to membrane potential and both gates close  
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relative refactory period   hyperpolarization occurs  
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axon hillock   has lots of Na+ channels, where action potential has to hit before it can rapidly continue down the axon  
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passive spread   action potential in the cell body because Na+ and K+ channels are not as efficiently distributed  
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nerve impulse   transmission and propagation of action potential along axon  
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myelin sheath   insulates axon at specific points to allow faster and farther propagation, made of Schwann cells  
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Nodes of Ranvier   where Schwann cells taper off, where action potentials are triggered on the axon  
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saltatory propagation   happens with myelin insulated axon, faster than continuous propagation  
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synapse   space between two adjacent neurons  
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electrical synapses   have gap junctions to connect neurons to help propagate signal  
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chemical synapse   synaptic cleft separates neurons, so neurotransmitters are needed to propagate signal  
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connexon   made of connex in subunits (proteins) that make up pore/channels between neurons  
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synaptic vesicles   contain neurotransmitters that bind to postsynaptic membrane receptors in exocytosis  
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ionotropic receptors   neurotransmitter acts as ligand and binds to receptor to open channel (direct)  
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metabotropic receptors   neurotransmitter binds to receptor and receptor signals for the channel to open (indirect)  
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excitatory receptor   depolarization of presynaptic neuron when neurotransmitter binds  
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inhibitory receptor   hyperpolarization when neurotransmitter binds  
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necessary properties of neurotransmitters   elicit appropriate response in synaptic cleft, occur naturally in presynaptic neuron, released at correct time  
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acetylcholine   type of neurotransmitter found in CNS, PNS, neuromuscular junctions that binds to cholinergic synapses  
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catecholamines   neurotransmitters that are derivitives of tyrosine synthesized in the adrenal gland, and bind to adrenergic synapses  
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dopamine   type of catecholamine neurotransmitter that is generally excitatory  
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norepinephrine   type of catecholamine neurotransmitter that is generally excitatory  
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seratonin   neurotransmitter that is a derivitive of tryptophan found in the CNS (controls sleep, memory, mood, appetite), and can be excitatory or inhibitory  
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amino acid neurotransmitters   glycine (inhibitory), glutamate (excitatory)  
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neuropeptides   neurotransmitters that are short chains of amino acids that can be inhibitory or excitatory and have longer lasting effects (enkephalines, pain perception)  
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synaptotagmin   Calcium sensor that tells vesicles when to go  
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nicotinic acetylcholine receptor (nAchR)   causes depolarization when 2 acetylcholine binds to alpha subunits  
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GABA receptor   causes hyperpolarization when gamma-aminobutyric acid binds  
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types of inactivation of neurotransmitters after release   degredation, re-uptake  
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temporal summation   signals from one neuron until action potential is made  
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spatial summation   take signals from many neurons to make action potential  
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Secretion of neurotransmitter step #1   action potential in bouton -> depolarization  
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Secretion of neurotransmitter step #2   depolarization -> voltage-gated calcium channel opens  
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Secretion of neurotransmitter step #3   calcium rushes into bouton (further depolarization) -> secretion  
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Secretion of neurotransmitter step #4   reserve vesicles move up for next action potential/diffusion of neurotransmitter across synaptic cleft to receptors on dendrite or soma  
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Secretion of neurotransmitter step #5   binding of neurotransmitters to receptors -> ion channels open  
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Secretion of neurotransmitter step #6   if threshold potential is reached in post synaptic neuron -> AP in post synaptic cell  
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