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pubmed-article:19764746pubmed:abstractTextWe present a procedure that supports the acquisition of (1)H-(15)N residual dipolar coupling (RDC) values for individual subunits in binary or ternary protein assemblies from a single experimental sample. Our method relies on asymmetric labeling of each subunit with the following scheme: species A uniformly with (15)N, species B uniformly with (15)N and (13)C, and species C uniformly with (15)N but selectively with (13)C' or (13)C(alpha). Because only a single sample is required, the approach obviates the need for preparing multiple samples and eliminates potential errors introduced from differences in sample conditions. Because numerous biological processes rely on protein assemblies or transient interactions, this method should be well suited for a wide range of future applications.lld:pubmed
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pubmed-article:19764746pubmed:authorpubmed-author:MarkleyJohn...lld:pubmed
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pubmed-article:19764746pubmed:dateRevised2011-7-26lld:pubmed
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pubmed-article:19764746pubmed:articleTitleOne-sample approach to determine the relative orientations of proteins in ternary and binary complexes from residual dipolar coupling measurements.lld:pubmed
pubmed-article:19764746pubmed:affiliationNational Magnetic Resonance Facility at Madison, Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706-1544, USA.lld:pubmed
pubmed-article:19764746pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19764746pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
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