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38 Cards in this Set
- Front
- Back
Progression through the secretory pathway: With permissive temp: the secretory pathway is active and _ of the IMP-GFP can be easily followed. fig 14.2
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transmission
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Yeast to genetically define the pathway: there are temp sensitive _ mutations and by alternating the temp to non-permissive then _ is blocked. fig 14.4
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sec
secretion |
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Progression through the secretory pathway with yeast: _ _ sys complement the yeast analysis. fig 14.5
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in vitro
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Vesicle traffic: there is a _ put on proteins to cause vesicle formation and eventually _. There are 6 basic components of coated vesicle: fig 14.6a
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coat
budding GTP-binding protein v-SNARE protein membrane cargo protein membrane cargo-receptor protein coat proteins |
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Vesicle traffic: coat is lost prior to _ with the membrane. fusion is mediated by Inter-membrane proteins called _. There are 2 types: 2 fig 14.6b
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fusion
SNAREs v-SNARE-vesicle membrane t-SNARE- target membrane |
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Secretory Pathway has two major concepts: 2
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vesicles
cisternal progression |
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Dif coats for dif vesicles: _ control the coat assembly aka small _ _ proteins
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G-protein
coat protein GTPase switch |
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Table 14.1
COPII vesicle is used to move from _ to _-_. COPI vesicle is used to move from _-_ to _. Clathrin and adapter proteins move _-_ to _ or _ _ to _ etc |
ER to cis-golgi
cis-golgi to ER trans-golgi to endosome, PM to endosome |
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Dif coats for dif vesicles: COPII is ER to cis-golgi
_ is the G-protein and _ is the GEF using Ran cycle. _-_ mediates COPII coat assembly. fig 14.8 after GTP is added to Sar1 and Sec12 a _ _-terminus is exposed |
Sar1
Sec12 Sar1-GTP hydrophobic N- |
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Dif coats for dif vesicles: COPII is ER to cis-golgi
_is the GAP which is activated after coat is assembled. When active GAP converts (hydrolysis) _-_ to _-_ <-- medicates coat disassembly. FYI recruitment of _-_, _ _ proteins, and _ _ receptors by coat proteins. fig 14.8 |
Sec23
Sar1-GTP to Sar1-GDP v-SNARE, membrane cargo, membrane cargo |
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Vesicle fusion: trans-golgi to PM: Along with v-SNARE and t-SNARE, there is a lipid-anchored _-_ on membrane and G-protein aka _ on vesicle. VAMP is the v_SNARE. (_ _ _ _). fig 14.10
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SNAP-25
Rab vesicle associated membrane protein |
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Vesicle fusion: fig 14.10
_-_ mediates docking to Rab effector. SNARE complex forms: (3). membranes fuse through _ _ to Rab-GDP, soluble NSF/alpha-SNAP use _ to disassemble SNARE complexes |
Rab-GTP
v-SNARE, t-SNARE, SNAP-25 GTP hydrolysis ATP |
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Vesicle traffic bn rER and cis-Golgi compartments: fig 14.11
2 types of vesicles: _ - rER to cis-Golgi, _ coated vesicles _ - cis-golgi to rER, _ coated vesicles |
anterograde
COPII retrograde COPI |
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COPII: rER to Golgi anterograde transport:
COPII= Sec23/Sec24 plus Sec13/Sec31 dimers _-_ recruits coat dimer via Sec23 and coat dimer binds cargo or receptor (via _). Signal sequence is _ _. fig 14.12 |
Sar1-GTP
Sec24 diacidic tripeptide (DXE) |
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COPI: Golgi to rER retroograde transport: fig 14.13
G-protein for assembly is _-_. Cargo signal sequence is _ for membrane and _ soluble. the path recycles proteins for reuse like with: (3) |
ARF-GTP
KKXX and KDEL KDEL receptor, v-SNARE, folding protein |
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transport from cis to medial to trans occurs by _ _ not vesicles. fig 14.17
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cisternal progression
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After secretion, protein vesicle is transport to endosomes- _ and _ _ (AP) complexes (3)
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clarthrin
adaptor protein AP1, AP3, GGA |
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Overview of Pathway Transport:Anterograde
rER to cis Golgi with _ _ cis to medial to trans golgi with _ _ trans golgi to late endosomes with _ _ trans golgi to lysosomes with _ _ |
COPII vesicles
cisternal progression clathrin ves. Ap ves. |
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Overview of Pathway Transport:Retrograde:
cis-golgi to eER with _ _ trans to medial to cis-golgi with _ _ PM to late endosomes with _ _ |
COPI ves.
COPI ves. clathrin ves. |
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Clathrin coated vesicles: G-protein for assembly: _-_ with hydrolyzes GTP, adpter proteins are (3)
_ or _- trans-golgi to endosome _- PM to endosome _- trans-golgi to lysosome and trans-golgi to PM |
ARF-GTP
AP1 or GGA AP2 AP3 |
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A vesicle formation is complete with _ which forms a ring around the neck of the forming vesicle. _ _ contracts the ring to help with fusion. _ and _ don't use GTPase to pinch off vesicles. fig 14.19
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dynamin
GTP hydrolysis COPI and COPII |
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Dynamin is required for pinching off clathrin-coated vesicles. In the presence of GTP-gamma-S, a non-hydrolyzable GTP derivative, dynamin can/cannot pinch off vesicles so it just accumulates around neck. fig 14.20
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cannot
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The _ receptor directs proteins to lysosomes. It stands for _- # -_ and is added to _-linked oligosaccharides on some proteins (hydrolytic enzymes) in the _-golgi
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M6P
mannose-6-phosphate N-linked cis-golgi |
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The M6P receptor involves proteins that have specificity recognized by _ _ which is then removed and makes _ a sorting signal. fig 14.21
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GlcNAc phosphotransferase
M6P |
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The M6P receptor directs proteins to lysosomes. it binds to proteins and is incorporated into _-_-coated vesicles. this occurs in the _-golgi and at the _. After formation, the _ _ disassembles.
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clathrin-AP
trans-golgi and PM vesicle coat |
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The M6P receptor directs proteins to lysosomes. Vesicles fuse with late endosomes and the specificity comes from identity of _-_ and _-_. Acidic pH causes _ of M6P receptor and cargo. The receptor is recycles back into the _-golgi
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v-SNARES
t-SNARES dissociation trans-golgi |
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The M6P receptor directs proteins to lysosomes process. fig 17.23
1 _-_ bud forms vesicle 2 coat is _. 3 _ receptor binds with late endosome 4 either protein is sent to _ and M6P receptor is recycled. 5 M6P receptor located on PM collects cargo and forms _-_ _. 6 clathrin-coated vesicle is formed from _-_ _. 7 _ is removed to form late endosome which has a low pH. |
1clathrin-coated
2removed 3M6P 4lysosome 5clathrin-coated pit 6receptor-mediated endocytosis 7clathrin |
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Some proteins undergo _ _ after leaving the trans-golgi. e.g. proinsulin in budding vesicles and immature secretory vesicles and _ is present in mature vesicles. fig 14.23
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proteolytic processing
insulin |
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_ require proteolytic cleavage to yield active proteins. for lysosomal proteins, this occurs in _ _ and _. For secreted proteins, this occurs in the immature _ _. With _ _ usually has one N-terminal cleavage site. fig 14-24
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proproteins
endosomes, lysosomes secretory vescicles constitutive secretion |
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Proproteins require proteolytic cleavage to yield active proteins: regulated secretion usually involves _ _. (3) are involved in regulated secretion. fig 14.24
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multiple cuts
Chromogranin A, Chromogranin B, Secretogranin II |
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Regulated secretion: e.g. synaptic vesicles: vesicles accumulate near _. There is an increase in _ _ that leads to _ _ in specific proteins which then leads to vesicle fusion with PM
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PM
intracellular Ca+2 conformational changes |
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Sorting proteins to apical or basolateral membranes: most epithelial cell types: _-_ proteins sort to the apical membrane but its not a sorting signal. In thyroid cells, GPI is targeted to _ _. fig 14.25
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GPI-anchored
basolateral membrane |
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Transcytosis can move ligands across _ _. e.g. delivery of antibodies from mother's milk to baby by _-_ conformational changes.
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epithelial sheets
pH-mediated |
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fig 14.26 receptor-mediated endocytosis is similar to _ pathway. e.g. uptake of lipoprotein complexes (LDL). receptor and cargo are targeted to _ _. _ _ releases cargo aka acidification and receptor is _.
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M6P
late endosomes pH drops recycled |
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pH-dependent cargo release is mediated by _ _. fig 14.30 e.g. LDL receptor is _. His is _ to change pH.
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conformational change
ApoB-100 protonated |
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Specialized vesicles deliver cell components to the lysosome for _. Multivesicular pathway fig 14.32
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degradation
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Retroviruses apparently use the _ _ to bud from the PM: It uses a _-_ of a specific peripheral membrane proteins to target assembly of _ complex, which leads to vesicle formation. ATP hydrolysis by _ then disassembles complexes. fig 14.34
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multivesicular pathway
ESCRT Vsp4 |
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Specialized vesicles deliver cell components to the lysosome for degradation: _ _ involves entire organelles like peroxisomes and mitochondria. fig 14.35
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authophagic pathway
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