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• W2605958254 abstract "The biophysical analysis of dynamically formed multi-protein complexes in solution presents a formidable technical challenge. Sedimentation velocity (SV) analytical ultracentrifugation achieves strongly size-dependent hydrodynamic resolution of different size species, and can be combined with multi-component detection by exploiting different spectral properties or temporally modulated signals from photoswitchable proteins. Coexisting complexes arising from self- or hetero-associations that can be distinguished in SV allow measurement of their stoichiometry, affinity, and cooperativity. However, assemblies that are short-lived on the time-scale of sedimentation (t1/2 < 100 sec) will exhibit an as of yet unexplored pattern of sedimentation boundaries governed by coupled co-migration of the entire system. Here, we present a theory for multi-component sedimentation of rapidly interacting systems, which reveals simple underlying physical principles, offers a quantitative framework for analysis, thereby extending the dynamic range of SV for studying multi-component interactions" @default.
• W2605958254 created "2017-04-28" @default.
• W2605958254 creator A5016735960 @default.
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• W2605958254 date "2017-04-10" @default.
• W2605958254 modified "2023-09-27" @default.
• W2605958254 title "Sedimentation of rapidly interacting multicomponent systems" @default.
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