Chiral and Structural Analysis of Biomolecules Using Mass Spectrometry and Ion Mobility-Mass Spectrometry

被引:42
|
作者
Enders, Jeffrey R. [2 ,3 ]
Mclean, John A. [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Dept Chem, Stevenson Ctr 7330, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Vanderbilt Inst Chem Biol, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Vanderbilt Inst Integrat Biosyst Res & Educ, Nashville, TN 37235 USA
关键词
chirality; mass spectrometry; ion mobility; ion mobility-mass spectrometry; structural separations; peptide; protein; VIBRATIONAL CIRCULAR-DICHROISM; RAMAN OPTICAL-ACTIVITY; FUNCTIONAL THEORY CALCULATIONS; LIQUID-CHROMATOGRAPHIC SEPARATION; ELECTROSPRAY-IONIZATION; GAS-PHASE; NONCOVALENT INTERACTIONS; PROTEIN-STRUCTURE; ENANTIOSELECTIVE COMPLEXATION; ABSOLUTE-CONFIGURATIONS;
D O I
10.1002/chir.20806
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This report describes the strategies for gas-phase chiral and structural characterization of biomolecules using mass spectrometry (MS) and ion mobility-MS (IM-MS) techniques. Because both MS and IM-MS do not directly provide chiral selectivity, methodologies for adding a chiral selector are discussed in the context of (i) host-guest (H-G) associations, (ii) diastereomeric collision-induced dissociation (CID) methods, (iii) ion-molecule reactions, and (iv) the kinetic method. MS techniques for the analysis of proteins and protein complexes are briefly described. New advances in performing rapid 2D gas-phase separations on the basis of IM-MS are reviewed with a particular emphasis on the different forms of IM instrumentation and how they are used for chiral and/or structural biomolecular studies. This report is not intended to be a comprehensive review of the field, but rather to underscore the contemporary techniques that are commonly or increasingly being used to complement measurements performed by chiroptical methodologies. Chirality 21:E253-E264, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:E253 / E264
页数:12
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