首页 | 本学科首页   官方微博 | 高级检索  
     


Membrane protein assembly into Nanodiscs
Authors:Timothy H. Bayburt
Affiliation:Department of Biochemistry, School of Molecular and Cellular Biology, University of Illinois, Urbana-Champaign, Urbana, IL 61801, United States
Abstract:Nanodiscs are soluble nanoscale phospholipid bilayers which can self-assemble integral membrane proteins for biophysical, enzymatic or structural investigations. This means for rendering membrane proteins soluble at the single molecule level offers advantages over liposomes or detergent micelles in terms of size, stability, ability to add genetically modifiable features to the Nanodisc structure and ready access to both sides of the phospholipid bilayer domain. Thus the Nanodisc system provides a novel platform for understanding membrane protein function. We provide an overview of the Nanodisc approach and document through several examples many of the applications to the study of the structure and function of integral membrane proteins.
Keywords:DDM, dodecylmaltoside   DMPC, dimyristoylphosphatidylcholine   DPPC, dipalmitoylphosphatidylcholine   MSP, membrane scaffold protein   OG, octylglucoside   PC, phosphatidylcholine   PL, phospholipid   POPC, 1-palmitoyl-2-oleoyl phosphatidylcholine   PS, phosphatidylserine   DOTAP, 1,2-dioleoyl-3-trimethylammonium-propane   PE, phosphatidylethanolamine   PG, phosphatidylglycerol   rHDL, reconstituted high density lipoprotein   SAXS, small angle X-ray scattering   SEC, size exclusion chromatography
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号