| Literature DB >> 27743406 |
Kyung Ho Cho1, Orquidea Ribeiro2, Yang Du3, Elena Tikhonova4, Jonas S Mortensen5, Kelsey Markham4, Parameswaran Hariharan4, Claus J Loland5, Lan Guan4, Brian K Kobilka3, Bernadette Byrne2, Pil Seok Chae1.
Abstract
Detergents serve as useful tools for membrane protein structural and functional studies. Their amphipathic nature allows detergents to associate with the hydrophobic regions of membrane proteins whilst maintaining the proteins in aqueous solution. However, widely used conventional detergents are limited in their ability to maintain the structural integrity of membrane proteins and thus there are major efforts underway to develop novel agents with improved properties. We prepared mesitylene-cored glucoside amphiphiles (MGAs) with three alkyl chains and compared these agents with previously developed xylene-linked maltoside agents (XMAs) with two alkyl chains and a conventional detergent (DDM). When these agents were evaluated for four membrane proteins including a G protein-coupled receptor (GPCR), some agents such as MGA-C13 and MGA-C14 resulted in markedly enhanced stability of membrane proteins compared to both DDM and the XMAs. This favourable behaviour is due likely to the increased hydrophobic density provided by the extra alkyl chain. Thus, this study not only describes new glucoside agents with potential for membrane protein research, but also introduces a new detergent design principle for future development.Entities:
Keywords: amphiphile design; detergents; membrane proteins; protein solubilisation; protein stabilization
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Year: 2016 PMID: 27743406 PMCID: PMC5500206 DOI: 10.1002/chem.201603338
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236