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Insights into the Mechanistic Dichotomy of the Protein Farnesyltransferase Peptide Substrates CVIM and CVLS
- Yang, Yue, Wang, Bing, Ucisik, Melek
N., Cui, Guanglei, Fierke, Carol A., Merz, Kenneth M.
- Journal of the American Chemical Society 2012 v.134 no.2 pp. 820-823
- geranylgeranyl diphosphate synthase, isotopes, tritium
- Protein farnesyltransferase (FTase) catalyzes farnesylation of a variety of peptide substrates. ³H α-secondary kinetic isotope effect (α-SKIE) measurements of two peptide substrates, CVIM and CVLS, are significantly different and have been proposed to reflect a rate-limiting SN2-like transition state with dissociative characteristics for CVIM, while, due to the absence of an isotope effect, CVLS was proposed to have a rate-limiting peptide conformational change. Potential of mean force quantum mechanical/molecular mechanical studies coupled with umbrella sampling techniques were performed to further probe this mechanistic dichotomy. We observe the experimentally proposed transition state (TS) for CVIM but find that CVLS has a symmetric SN2 TS, which is also consistent with the absence of a ³H α-SKIE. These calculations demonstrate facile substrate-dependent alterations in the transition state structure catalyzed by FTase.