4.6 Article

Rapid and selective detection of fatty acylated proteins using omega-alkynyl-fatty acids and click chemistry

Journal

JOURNAL OF LIPID RESEARCH
Volume 51, Issue 6, Pages 1566-1580

Publisher

ELSEVIER
DOI: 10.1194/jlr.D002790

Keywords

myristoylation; palmitoylation; mitochondria; membranes; enzymes

Funding

  1. CIHR [MOP 81248]
  2. AHFMR
  3. Alberta Cancer Research Institute
  4. University of British Columbia's Child & Family Research Institute
  5. Canadian Foundation for Innovation
  6. Michael Smith Foundation for Health Research
  7. National Institutes of Health [GM-58867, GM-31278]
  8. Robert A. Welch Foundation
  9. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM058867, R01GM031278, R37GM058867] Funding Source: NIH RePORTER

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Progress in understanding the biology of protein fatty acylation has been impeded by the lack of rapid direct detection and identification methods. We first report that a synthetic omega-alkynyl-palmitate analog can be readily and specifically incorporated into GAPDH or mitochondrial 3-hydroxyl-3-methylglutaryl-CoA synthase in vitro and reacted with an azido-biotin probe or the fluorogenic probe 3-azido-7-hydroxycoumarin using click chemistry for rapid detection by Western blotting or flat bed fluorescence scanning. The acylated cysteine residues were confirmed by MS. Second, omega-alkynyl-palmitate is preferentially incorporated into transiently expressed H- or N-Ras proteins (but not non-palmitoylated K-Ras), compared with omega-alkynyl-myristate or omega-alkynyl-stearate, via an alkali sensitive thioester bond. Third, omega-alkynyl-myristate is specifically incorporated into endogenous co- and posttranslationally myristoylated proteins. The competitive inhibitors 2-bromopalmitate and 2-hydroxymyristate prevented incorporation of omega-alkynyl-palmitate and omega-alkynyl-myristate into palmitoylated and myristoylated proteins, respectively. Labeling cells with omega-alkynyl-palmitate does not affect membrane association of N-Ras. Furthermore, the palmitoylation of endogenous proteins including H- and N-Ras could be easily detected using omega-alkynyl-palmitate as label in cultured HeLa, Jurkat, and COS-7 cells, and, promisingly, in mice. The omega-alkynyl-myristate and -palmitate analogs used with click chemistry and azido-probes will be invaluable to study protein acylation in vitro, in cells, and in vivo.-Yap, M. C., M. A. Kostiuk, D. D. O. Martin, M. A. Perinpanayagam, P. G. Hak, A. Siddam, J. R. Majjigapu, G. Rajaiah, B. O. Keller, J. A. Prescher, P. Wu, C. R. Bertozzi, J. R. Falck, and L. G. Berthiaume. Rapid and selective detection of fatty acylated proteins using omega-alkynyl-fatty acids and click chemistry. J. Lipid Res. 2010. 51: 1566-1580.

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