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#1
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| > CD and fluorescence give you information about secondary structure, not shape. I really mean shape: oval, globular, rod-like, straight, bent, etc.. No unfolding involved in transition between different "shapes" and probably little 2nd structure modification. No, crystallography or EM are not viable options. Carlo |
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#2
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| Carlo Zambonelli wrote: In that case, information on shape will be incomplete, but you may be able to get coarse figures like for example the ratio of the eliptical axes of a protein. In as far as conformational changes affect the molecular hydrodynamics of a protein small angle neutron or light scattering, analytical ultracentrifugation, gel filtration or native electrophoresis can follow them. Full interpretation however will not be possible without more detailed data on the endpoint-structures. |
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| change , detection , protein , proteinanalysis , shape |
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