Affiliation:
1. Faculty of Chemistry Institute of Biological Chemistry University of Vienna Währinger Str. 38 1090 Vienna Austria
Abstract
AbstractStructure determination lies at the heart of many biochemical research programs. However, the “giants”: X‐ray diffraction, electron microscopy, molecular dynamics simulations, and nuclear magnetic resonance, among others, leave quite a few dark spots on the structural pictures drawn of proteins, nucleic acids, membranes, and other biomacromolecules. For example, structural models under physiological conditions or of short‐lived intermediates often remain out of reach of the established experimental methods. This account frames the possibility of including hyperpolarized, that is, dramatically signal‐enhanced NMR in existing workflows to fill these spots with detailed depictions. We highlight how integrating methods based on dissolution dynamic nuclear polarization can provide valuable complementary information about formerly inaccessible conformational spaces for many systems. A particular focus will be on hyperpolarized buffers to facilitate the NMR structure determination of challenging systems.
Subject
Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry
Cited by
5 articles.
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