Robust, high-throughput solution structural analyses by small angle X-ray scattering (SAXS).
Robust, high-throughput solution structural analyses by small angle X-ray scattering (SAXS).
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DOI:
10.1038/nmeth.1353
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发表时间:
2009-08
期刊:
影响因子:
48
通讯作者:
Tainer, John A.
中科院分区:
文献类型:
--
作者:
Hura, Greg L.;Menon, Angeli L.;Hammel, Michal;Rambo, Robert P.;Poole, Farris L., II;Tsutakawa, Susan E.;Jenney, Francis E., Jr.;Classen, Scott;Frankel, Kenneth A.;Hopkins, Robert C.;Yang, Sung-jae;Scott, Joseph W.;Dillard, Bret D.;Adams, Michael W. W.;Tainer, John A.
We present an efficient pipeline enabling high-throughput analysis of protein structure in solution with small angle X-ray scattering (SAXS). Our SAXS pipeline combines automated sample handling of microliter volumes, temperature and anaerobic control, rapid data collection, data analysis, and couples structural analysis with automated archiving. We subjected 50 representative proteins, mostly from Pyrococcus furiosus, to this pipeline, revealing that 30 were multimeric structures in solution. SAXS analysis allowed us to distinguish aggregated and unfolded proteins, define global structural parameters and oligomeric states for most samples, identify shapes and similar structures for 25 unknown structures, and determine envelopes for 41 proteins. We believe that high throughput SAXS is an enabling technology that may change the way that structural genomics research is done.
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