Investigating macromolecules inside cultured and injected cells by in-cell NMR spectroscopy

被引:106
作者
Serber, Zach
Selenko, Philipp
Haensel, Robert
Reckel, Sina
Loehr, Frank
Ferrell, James E., Jr.
Wagner, Gerhard
Doetsch, Volker
机构
[1] Univ Frankfurt, Inst Biophys Chem, D-60438 Frankfurt, Germany
[2] Stanford Univ, Sch Med, Dept Chem & Syst Biol, Stanford, CA 94305 USA
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
关键词
D O I
10.1038/nprot.2006.181
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The noninvasive character of NMR spectroscopy, combined with the sensitivity of the chemical shift, makes it ideally suited to investigate the conformation, binding events and dynamics of macromolecules inside living cells. These 'in-cell NMR' experiments involve labeling the macromolecule of interest with a nonradioactive but NMR-active isotope (N-15 or C-13). Cellular samples are prepared either by selectively overexpressing the protein in suitable cells ( e. g., bacterial cells grown on isotopically labeled media), or by injecting isotopically labeled proteins directly into either cells or cell extracts. Here we provide detailed protocols for in-cell NMR experiments in the prokaryotic organism Escherichia coli, as well as eukaryotic cells and extracts employing Xenopus laevis oocytes or egg extracts. In-cell NMR samples with proteins overexpressed in E. coli can be produced within 13-14 h. Preparing Xenopus oocyte samples for in-cell NMR experiments takes 6-14 h depending on the oocyte preparation scheme and the injection method used.
引用
收藏
页码:2701 / 2709
页数:9
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