4.7 Article

Collision Cross Sections for Structural Proteomics

期刊

STRUCTURE
卷 23, 期 4, 页码 791-799

出版社

CELL PRESS
DOI: 10.1016/j.str.2015.02.010

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资金

  1. Carl Trygger Foundation for Scientific Research
  2. Swedish Royal Academy of Sciences
  3. Helge Ax:son Johnson Foundation
  4. Swiss National Science Foundation
  5. BBSRC
  6. Royal Society University Research Fellowship
  7. Medical Research Council
  8. Biotechnology and Biological Sciences Research Council [BB/K004247/1]
  9. BBSRC [BB/J014346/1, BB/K004247/1] Funding Source: UKRI
  10. MRC [G1000819, MC_PC_13073] Funding Source: UKRI
  11. Biotechnology and Biological Sciences Research Council [BB/J014346/1, BB/K004247/1] Funding Source: researchfish
  12. Medical Research Council [G1000819, MC_PC_13073] Funding Source: researchfish

向作者/读者索取更多资源

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.

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