| Literature DB >> 19113834 |
Gary J Pielak1, Conggang Li, Andrew C Miklos, Alexander P Schlesinger, Kristin M Slade, Gui-Fang Wang, Imola G Zigoneanu.
Abstract
Almost everything we know about protein biophysics comes from studies on purified proteins in dilute solution. Most proteins, however, operate inside cells where the concentration of macromolecules can be >300 mg/mL. Although reductionism-based approaches have served protein science well for more than a century, biochemists now have the tools to study proteins under these more physiologically relevant conditions. We review a part of this burgeoning postreductionist landscape by focusing on high-resolution protein nuclear magnetic resonance (NMR) spectroscopy, the only method that provides atomic-level information over an entire protein under the crowded conditions found in cells.Entities:
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Year: 2009 PMID: 19113834 PMCID: PMC2645539 DOI: 10.1021/bi8018948
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162