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Sci. STKE, 31 October 2006
Vol. 2006, Issue 359, p. re14
[DOI: 10.1126/stke.3592006re14]
REVIEWS
Palmitoylation of Ligands, Receptors, and Intracellular Signaling Molecules
Marilyn D. Resh*
Cell Biology Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, Box 143, New York, NY 10021, USA.
Abstract:
Palmitate, a 16-carbon saturated fatty acid, is attached to more than 100 proteins. Modification of proteins by palmitate has pleiotropic effects on protein function. Palmitoylation can influence membrane binding and membrane targeting of the modified proteins. In particular, many palmitoylated proteins concentrate in lipid rafts, and enrichment in rafts is required for efficient signal transduction. This Review focuses on the multiple effects of palmitoylation on the localization and function of ligands, receptors, and intracellular signaling proteins. Palmitoylation regulates the trafficking and function of transmembrane proteins such as ion channels, neurotransmitter receptors, heterotrimeric guanine nucleotidebinding protein (G protein)coupled receptors, and integrins. In addition, immune receptor signaling relies on protein palmitoylation at many levels, including palmitoylated co-receptors, Src family kinases, and adaptor or scaffolding proteins. The localization and signaling capacities of Ras and G proteins are modulated by dynamic protein palmitoylation. Cycles of palmitoylation and depalmitoylation allow H-Ras and G protein subunits to reversibly bind to and signal from different intracellular cell membranes. Moreover, secreted ligands such as Hedgehog, Wingless, and Spitz use palmitoylation to regulate the extent of long- or short-range signaling. Finally, palmitoylation can alter signaling protein function by direct effects on enzymatic activity and substrate specificity. The identification of the palmitoyl acyltransferases has provided new insights into the biochemistry of this posttranslational process and permitted new substrates to be identified.
Palmitoylation of Cytoskeleton Associated Protein 4 by DHHC2 Regulates Antiproliferative Factor-mediated Signaling.
S. L. Planey, S. K. Keay, C.-O. Zhang, and D. A. Zacharias (2009)
Mol. Biol. Cell
20, 1454-1463
|Abstract »|Full Text »|PDF »
2-Bromopalmitate and 2-(2-hydroxy-5-nitro-benzylidene)-benzo[b]thiophen-3-one inhibit DHHC-mediated palmitoylation in vitro.
B. C. Jennings, M. J. Nadolski, Y. Ling, M. B. Baker, M. L. Harrison, R. J. Deschenes, and M. E. Linder (2009)
J. Lipid Res.
50, 233-242
|Abstract »|Full Text »|PDF »
CSS-Palm 2.0: an updated software for palmitoylation sites prediction.
J. Ren, L. Wen, X. Gao, C. Jin, Y. Xue, and X. Yao (2008)
Protein Eng. Des. Sel.
21, 639-644
|Abstract »|Full Text »|PDF »
Rapid detection, discovery, and identification of post-translationally myristoylated proteins during apoptosis using a bio-orthogonal azidomyristate analog.
D. D. O. Martin, G. L. Vilas, J. A. Prescher, G. Rajaiah, J. R. Falck, C. R. Bertozzi, and L. G. Berthiaume (2008)
FASEB J
22, 797-806
|Abstract »|Full Text »|PDF »
Identification of palmitoylated mitochondrial proteins using a bio-orthogonal azido-palmitate analogue.
M. A. Kostiuk, M. M. Corvi, B. O. Keller, G. Plummer, J. A. Prescher, M. J. Hangauer, C. R. Bertozzi, G. Rajaiah, J. R. Falck, and L. G. Berthiaume (2008)
FASEB J
22, 721-732
|Abstract »|Full Text »|PDF »
Control of Inward Rectifier K Channel Activity by Lipid Tethering of Cytoplasmic Domains.
D. Enkvetchakul, I. Jeliazkova, J. Bhattacharyya, and C. G. Nichols (2007)
J. Gen. Physiol.
|Abstract »|Full Text »|PDF »
Cellular palmitoylation and trafficking of lipidated peptides.