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    Biochemistry. 2009 Jan 20;48(2):226-34.

    Protein nuclear magnetic resonance under physiological conditions.

    Pielak GJ, Li C, Miklos AC, Schlesinger AP, Slade KM, Wang GF, Zigoneanu IG.

    Department of Chemistry, Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina 27599, USA. gary_pielak@unc.edu

    Erratum in:

    • Biochemistry. 2009 Sep 29;48(38):9170.

    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.

    PMID: 19113834 [PubMed - indexed for MEDLINE]

    PMCID: 2645539

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