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用于结构蛋白质组学的碰撞截面。

Collision cross sections for structural proteomics.

机构信息

Department of Chemistry, Physical & Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, Oxfordshire, OX1 3QZ, UK.

Department of Chemistry, Physical & Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, Oxfordshire, OX1 3QZ, UK.

出版信息

Structure. 2015 Apr 7;23(4):791-9. doi: 10.1016/j.str.2015.02.010. Epub 2015 Mar 19.

Abstract

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.

摘要

离子淌度质谱(IM-MS)通过报告其碰撞截面(CCS)来实现对生物分子的结构分析。在结构蛋白质组学中利用 IM-MS 的主要瓶颈在于缺乏将结构和模型与实验数据相关联的速度。在这里,我们提出了 IMPACT(离子淌度投影逼近计算工具),它克服了这两个挑战,提供了高达 10^6 倍于其他方法的准确 CCS。这使我们能够评估整个结构蛋白质组呈现的 CCS 空间,研究蛋白质构象的集合,并监测分子动力学轨迹。我们的数据表明,CCS 是一个高度信息丰富的参数,IM-MS 对结构生物学家具有相当大的实际价值。

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