Sievers Susanne
Department of Microbial Physiology and Molecular Biology, Institute for Microbiology, University of Greifswald, Greifswald, Germany.
Methods Mol Biol. 2018;1841:21-33. doi: 10.1007/978-1-4939-8695-8_3.
This protocol represents a detailed instruction how to prepare protein samples in order to raise mass spectrometry-based identification and quantification rates with respect to the challenging class of membrane proteins. This will increase comprehensiveness of global proteome studies on the one hand but could also be of interest for researchers targeting specific membrane proteins or membrane protein sequences on the other hand. The protocol is a composite of two parts, one focusing on the identification of protein sequences exterior to a cellular membrane (loops of integral membrane proteins, peripheral membrane proteins), and the other part targeting primarily protein domains spanning the lipid bilayer. The feasibility of the protocol, as it is described here, was originally shown for the gram-positive pathogenic bacterium Staphylococcus aureus but should be applicable to any kind of membrane protein.
本方案提供了详细的指导说明,介绍了如何制备蛋白质样品,以便在针对具有挑战性的膜蛋白类别时提高基于质谱的鉴定和定量率。一方面,这将提高全球蛋白质组研究的全面性;另一方面,对于针对特定膜蛋白或膜蛋白序列的研究人员来说也可能具有重要意义。该方案由两部分组成,一部分侧重于鉴定细胞膜外部的蛋白质序列(整合膜蛋白的环、外周膜蛋白),另一部分主要针对跨越脂质双层的蛋白质结构域。此处所述方案的可行性最初是在革兰氏阳性病原菌金黄色葡萄球菌中得到验证的,但应该适用于任何种类的膜蛋白。