X-ray solution scattering (SAXS) combined with crystallography and computation: defining accurate macromolecular structures, conformations and assemblies in solution.

X-ray solution scattering (SAXS) combined with crystallography and computation: defining accurate macromolecular structures, conformations and assemblies in solution.
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DOI:
10.1016/j.bpj.2010.12.409
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发表时间:
2011-02
影响因子:
6.1
通讯作者:
C. Putnam;M. Hammel;Greg L. Hura;J. Tainer
C. Putnam;M. Hammel;Greg L. Hura;J. Tainer
中科院分区:
生物学2区
文献类型:
--
作者:
C. Putnam;M. Hammel;Greg L. Hura;J. Tainer

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Protein, DNA, and RNA shape, assembly and interactions shapes, plus their detailed structural chemistry, encode key information regarding pathway choices and biological outcomes. We are developing SAXS combined with crystallography as a premiere tool for defining macromolecular conformations and connections suitable to join proteins to pathways and at the proteomic scale 1-2. Crystallography supplies unsurpassed structural detail for mechanistic analyses; however, it is restricted to describing conformations of macromolecules within crystal lattices. In principle, SAXS can provide reliable complementary data on small and large macromolecules 3. In practice, SAXS can be limited by problems in optimizing samples and analyses, which can be reduced or avoided. Our results on dynamic RNA, DNA, and protein complexes show that SAXS has great potential to provide accurate shapes, conformations, and assembly states in solution and inform biological functions in fundamental ways 4-5.