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ACS Cent Sci. 2020 Apr 22;6(4):573-588. doi: 10.1021/acscentsci.0c00080. Epub 2020 Apr 10.
2
Design and Performance of a Second-Generation Surface-Induced Dissociation Cell for Fourier Transform Ion Cyclotron Resonance Mass Spectrometry of Native Protein Complexes.第二代用于傅里叶变换离子回旋共振质谱分析天然蛋白复合物的表面诱导解吸池的设计与性能。
Anal Chem. 2019 Nov 5;91(21):14049-14057. doi: 10.1021/acs.analchem.9b03746. Epub 2019 Oct 22.
3
Relative interfacial cleavage energetics of protein complexes revealed by surface collisions.通过表面碰撞揭示蛋白质复合物的相对界面断裂能。
Proc Natl Acad Sci U S A. 2019 Apr 23;116(17):8143-8148. doi: 10.1073/pnas.1817632116. Epub 2019 Apr 3.
4
Surface-Induced Dissociation of Noncovalent Protein Complexes in an Extended Mass Range Orbitrap Mass Spectrometer.在扩展质量范围轨道阱质谱仪中表面诱导的非共价蛋白质复合物的解离。
Anal Chem. 2019 Mar 5;91(5):3611-3618. doi: 10.1021/acs.analchem.8b05605. Epub 2019 Feb 12.
5
Topological Analysis of Transthyretin Disassembly Mechanism: Surface-Induced Dissociation Reveals Hidden Reaction Pathways.转甲状腺素蛋白解组装机制的拓扑分析:表面诱导的解离揭示了隐藏的反应途径。
Anal Chem. 2019 Feb 5;91(3):2345-2351. doi: 10.1021/acs.analchem.8b05066. Epub 2019 Jan 28.
6
Localization of Protein Complex Bound Ligands by Surface-Induced Dissociation High-Resolution Mass Spectrometry.通过表面诱导解吸高分辨质谱定位蛋白质复合物结合配体。
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7
Surface-Induced Dissociation of Protein Complexes in a Hybrid Fourier Transform Ion Cyclotron Resonance Mass Spectrometer.在混合傅里叶变换离子回旋共振质谱仪中,蛋白质复合物的表面诱导解离。
Anal Chem. 2017 Jan 3;89(1):895-901. doi: 10.1021/acs.analchem.6b03986. Epub 2016 Dec 15.
8
Dynamics of Protonated Peptide Ion Collisions with Organic Surfaces: Consonance of Simulation and Experiment.质子化肽离子与有机表面的碰撞动力学:模拟与实验的一致性
J Phys Chem Lett. 2016 Aug 18;7(16):3142-50. doi: 10.1021/acs.jpclett.6b00978. Epub 2016 Aug 2.
9
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Surface-Induced Dissociation of Homotetramers with D2 Symmetry Yields their Assembly Pathways and Characterizes the Effect of Ligand Binding.具有D2对称性的同四聚体的表面诱导解离产生其组装途径并表征配体结合的影响。
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倾斜表面和离子地毯阵列用于 SID。

A Tilted Surface and Ion Carpet Array for SID.

出版信息

J Am Soc Mass Spectrom. 2020 Feb 5;31(2):458-462. doi: 10.1021/jasms.9b00009. Epub 2019 Dec 24.

DOI:10.1021/jasms.9b00009
PMID:32031394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7203677/
Abstract

The development of native mass spectrometry (MS) has provided structural biologists an additional tool to probe the structures of large macromolecular systems. Surface-induced dissociation (SID) is one activation method used within tandem MS experiments that has proven useful in interrogating the connectivity and topology of biologically-relevant protein complexes. We present here the use of a tilted surface and ion carpet array within a new SID device design, enabling decreased dimensions along the ion path and fewer lenses to tune. This device works well in fragmenting ions of both low (peptides) and high (protein complexes) . Results show that the ion carpet array, while enabling simplification of the back-end of the device, has deficiencies in product collection and subsequently signal at higher SID energies when fragmenting protein complexes. However, the use of the tilted surface is advantageous as an effective way to shorten the device and reduce the number of independent voltages.

摘要

本土质谱(MS)的发展为结构生物学家提供了另一种工具,用于探测大型大分子系统的结构。表面诱导解离(SID)是串联 MS 实验中使用的一种激活方法,它在研究生物相关蛋白质复合物的连接和拓扑结构方面非常有用。我们在这里介绍了在新的 SID 设备设计中使用倾斜表面和离子地毯阵列,这使得沿离子路径的尺寸减小,并且需要调整的透镜更少。该设备在碎裂低(肽)和高(蛋白质复合物)离子时都能很好地工作。结果表明,虽然离子地毯阵列能够简化设备的后端,但在碎裂蛋白质复合物时,在产物收集方面存在缺陷,进而在更高的 SID 能量下信号强度降低。然而,倾斜表面的使用是一种有效的缩短设备和减少独立电压数量的方法。