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#coat proteins

2 public questions tagged with this topic.

The vesicle coat assembly process is initiated by:

Coat assembly regulated spatiotemporally to occur only at correct donor membranes and when cargo present ensuring energy not wasted. Initiating event activation of small GTPases Sar1 and ARF families from GDP cytosolic to GTP membrane state. Sar1 activated by Sec12 GEF integral ER protein exchanges GDP for GTP exposing amphipathic helix embedding ER leaflet inducing curvature recruiting Sec23-Sec24 heterodimer. Similarly ARF1 activated by GBF1 at ERGIC cis-Golgi and BIG1/2 at TGN upon membrane recruitment exposes myristoylated helix plus effector binding switch regions recruiting COPI coatomer heptamer or AP1/GGA clathrin adaptors beginning lattice nucleation. GTPases serve as membrane-anchored nucleation points; GDP form cytosolic inactive unable to bind coats. Direct clathrin triskelia binding membrane without adaptor or GTPase does not occur physiologically. ATP hydrolysis by NSF drives cis-SNARE disassembly post-fusion not coat initiation. Cargo phosphorylation may modulate adaptor affinity via casein kinase but nucleation itself requires active GTPase switch explaining sensitivity to fungal metabolite brefeldin A stabilizing abortive ARF-GDP-GEF complex and to non-hydrolyzable GTPgammaS locking coats on membranes preventing recycling and fusion competence.

Ref: Lee & Miller, Annu Rev Cell Dev Biol: Sar1 and ARF GTPases initiate coat assembly.

Which coat protein mediates retrograde transport from the Golgi to ER?

Retrieval pathways restoring escaped ER proteins and itinerant SNAREs rely on COPI coat protein complex I heptamer. COPI subunits alpha, beta, beta prime, gamma, delta, epsilon, zeta assemble 600 kDa coatomer. At Golgi cisternae and ERGIC tubules ARF1-GTP generated by GBF1 GEF recruits en bloc coatomer via gamma-beta-delta trunk interaction. Membrane deformation creates 50-60 nm vesicles containing cargo exposing KKXX or KXKXX dilysine motif at C-terminus binding WD40 propeller of alpha and beta prime COP subunits and KDEL receptor-cargo complexes where receptor tail contains KKXX-like signals. COPII comprising Sec23-24 and Sec13-31 does outward ER to Golgi leg recognizing di-acidic motifs, while clathrin plus AP1 AP2 GGA serves trans-Golgi-to-endosome and plasma-membrane-to-endosome routes sorting via tyrosine and dileucine. AP3 can function with clathrin or as non-clathrin coat for lysosomal membrane proteins. Pharmacologic blockade brefeldin A inhibits ARF GEF collapsing Golgi into ER within minutes by blocking COPI assembly. Hence COPI dedicated retrograde Golgi-to-ER carrier essential for ER proteostasis recycling SNAREs and maintaining Golgi enzyme gradients during cisternal maturation and homeostasis.

Ref: Alberts et al., MBC: COPI coat mediates retrograde Golgi-to-ER transport and retrieval.