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Tom W. Knapman Victoria L. Morton Nicola J. Stonehouse Peter G. Stockley Alison E. Ashcroft 《Rapid communications in mass spectrometry : RCM》2010,24(20):3033-3042
We have combined ion mobility spectrometry–mass spectrometry with tandem mass spectrometry to characterise large, non‐covalently bound macromolecular complexes in terms of mass, shape (cross‐sectional area) and stability (dissociation) in a single experiment. The results indicate that the quaternary architecture of a complex influences its residual shape following removal of a single subunit by collision‐induced dissociation tandem mass spectrometry. Complexes whose subunits are bound to several neighbouring subunits to create a ring‐like three‐dimensional (3D) architecture undergo significant collapse upon dissociation. In contrast, subunits which have only a single neighbouring subunit within a complex retain much of their original shape upon complex dissociation. Specifically, we have determined the architecture of two transient, on‐pathway intermediates observed during in vitro viral capsid assembly. Knowledge of the mass, stoichiometry and cross‐sectional area of each viral assembly intermediate allowed us to model a range of potential structures based on the known X‐ray structure of the coat protein building blocks. Comparing the cross‐sectional areas of these potential architectures before and after dissociation provided tangible evidence for the assignment of the topologies of the complexes, which have been found to encompass both the 3‐fold and the 5‐fold symmetry axes of the final icosahedral viral shell. Such insights provide unique information about virus assembly pathways that could allow the design of anti‐viral therapeutics directed at the assembly step. This methodology can be readily applied to the structural characterisation of many other non‐covalently bound macromolecular complexes and their assembly pathways. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
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Zhengjie He Susan Laurens Xavier M. Mbianda Agnes M. Modro Tom A. Modro 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6-7):1689-1692
This work summarizes studies on the preparation, structure, and reactivity of a new heterocyclic system containing phosphorus and nitrogen: 2,8-disubstituted-2,5,8-triaza-1 u 5 -phosphabicyclo[3.3.0]octane 1-oxide (and 1-sulfide). 相似文献
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Receptors ferrocene–triazole–pyridine triads assembled with Zn(II) or Cd(II) metal cations behave as chemosensor molecules for HSO4 ? anions through electrochemical and optical channels: the redox peak of the ferrocene/ferrocenium redox couple is shifted cathodically by 72–53 mV, and a new absorption band appeared in the UV–vis spectrum upon complexation with the HSO4 ? anion. Association constants, detection limits and stoichiometries of the recognition processes have been determined, whereas 1H NMR experiments and density functional theory calculations are used to suggest the plausible binding mode taking place in the new supramolecular assembly formed. 相似文献
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