Chemistry Publications

Title

Membrane Protein Structural Insights from Chemical Labeling and Mass Spectrometry

Document Type

Article

Publication Date

6-2010

Journal

Analyst

Volume

135

Issue

6

First Page

1191

Last Page

1200

URL with Digital Object Identifier

http://dx.doi.org/10.1039/b924805f

Abstract

Membrane proteins play a central role in virtually all biological processes, and they represent important drug targets. Unfortunately, the application of traditional high-resolution methods such as X-ray crystallography and NMR spectroscopy to membrane proteins remains challenging. This article reviews alternative approaches that involve chemical labeling and mass spectrometry (MS) for gaining insights into membrane protein structure, function, and interactions. Hydrogen/deuterium exchange MS represents an interesting avenue for exploring biomolecular conformations and dynamics, but thus far this technique has not been widely adopted for membrane protein studies. The main focus of this article is on the use of labeling agents that introduce covalent modifications in solvent-accessible protein regions. While it is possible to monitor the occurrence of single-site modifications using traditional biochemical methods or optical spectroscopy, the use of MS greatly enhances the scope and potential of this approach because multiple tagging events can be detected in parallel. The traditional bottom-up workflow of these studies involves the digestion of a chemically labeled membrane protein by a specific protease such as trypsin. This is followed by chromatographic separation of the resulting peptides and on-line electrospray ionization MS. The application of tandem MS allows pinpointing the exact locations of chemical modifications. A particularly exciting aspect is the applicability of covalent labeling techniques to membrane protein within their natural lipid environment, or even inside living cells. Some of these concepts will be illustrated using the oxidative labeling of bacteriorhodopsin as an example, but numerous other labeling agents and protein systems are being highlighted as well. It is hoped that this review will stimulate further developments in the characterization of membrane proteins.