Collision Cross Sections for Structural Proteomics

被引:214
作者
Marklund, Erik G. [1 ]
Degiacomi, Matteo T. [1 ]
Robinson, Carol V. [1 ]
Baldwin, Andrew J. [1 ]
Benesch, Justin L. P. [1 ]
机构
[1] Univ Oxford, Dept Chem, Phys & Theoret Chem Lab, Oxford OX1 3QZ, Oxon, England
基金
瑞士国家科学基金会; 英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
MOBILITY-MASS-SPECTROMETRY; GAS-PHASE PROTEINS; MACROMOLECULAR ASSEMBLIES; MOLECULAR-DYNAMICS; COMPLEXES; SCATTERING; BIOLOGY; IONS; RECOGNITION; DIFFUSION;
D O I
10.1016/j.str.2015.02.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ion mobility mass spectrometry (IM-MS) allows the structural interrogation of biomolecules by reporting their collision cross sections (CCSs). The major bottleneck for exploiting IM-MS in structural proteomics lies in the lack of speed at which structures and models can be related to experimental data. Here we present IMPACT (Ion Mobility Projection Approximation Calculation Tool), which overcomes these twin challenges, providing accurate CCSs up to 10 6 times faster than alternative methods. This allows us to assess the CCS space presented by the entire structural proteome, interrogate ensembles of protein conformers, and monitor molecular dynamics trajectories. Our data demonstrate that the CCS is a highly informative parameter and that IM-MS is of considerable practical value to structural biologists.
引用
收藏
页码:791 / 799
页数:9
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