Wilson D W, Whiteheart S W, Wiedmann M, Brunner M, Rothman J E
Program in Cellular Biochemistry and Biophysics, Rockefeller Research Laboratory, Sloan-Kettering Institute, New York 10021.
J Cell Biol. 1992 May;117(3):531-8. doi: 10.1083/jcb.117.3.531.
The N-ethylmaleimide sensitive fusion protein (NSF) is required for fusion of lipid bilayers at many locations within eukaryotic cells. Binding of NSF to Golgi membranes is known to require an integral membrane receptor and one or more members of a family of related soluble NSF attachment proteins (alpha-, beta-, and gamma-SNAPs). Here we demonstrate the direct interaction of NSF, SNAPs and an integral membrane component in a detergent solubilized system. We show that NSF only binds to SNAPs in the presence of the integral receptor, resulting in the formation of a multisubunit protein complex with a sedimentation coefficient of 20S. Particle assembly reveals striking differences between members of the SNAP protein family; gamma-SNAP associates with the complex via a binding site distinct from that used by alpha- and beta-SNAPs, which are themselves equivalent, alternative subunits of the particle. Once formed, the 20S particle is subsequently able to disassemble in a process coupled to the hydrolysis of ATP. We suggest how cycles of complex assembly and disassembly could help confer specificity to the generalized NSF-dependent fusion apparatus.
N - 乙基马来酰亚胺敏感融合蛋白(NSF)在真核细胞内的许多位置对于脂质双层的融合是必需的。已知NSF与高尔基体膜的结合需要一种整合膜受体以及一族相关可溶性NSF附着蛋白(α -、β - 和γ - SNAPs)中的一个或多个成员。在这里,我们在去污剂溶解系统中证明了NSF、SNAPs和一种整合膜成分之间的直接相互作用。我们表明,NSF仅在整合受体存在的情况下与SNAPs结合,从而形成沉降系数为20S的多亚基蛋白复合物。颗粒组装揭示了SNAP蛋白家族成员之间的显著差异;γ - SNAP通过与α - 和β - SNAPs不同的结合位点与复合物结合,α - 和β - SNAPs本身是该颗粒等效的、可替代的亚基。一旦形成,20S颗粒随后能够在与ATP水解偶联的过程中解离。我们提出复合物组装和解离的循环如何有助于赋予通用的NSF依赖性融合装置特异性。