Organometallic mechanism of action and inhibition of the 4Fe-4S isoprenoid biosynthesis protein GcpE (IspG)

摘要

We report the results of a series of chemical, EPR, ENDOR, and HYSCORE spectroscopic investigations of the mechanism of action (and inhibition) of GcpE, E-1-hydroxy-2-methyl-but-2-enyl-4-dipho-sphate (HMBPP) synthase, also known as IspG, an Fe_4S_4 cluster-containing protein. We find that the epoxide of HMBPP when reduced by GcpE generates the same transient EPR species as observed on addition of the substrate, 2-C-methyl-D-erythritol-2,4-cyc/o-dipho-sphate. ENDOR and HYSCORE spectra of these transient species (using ~2H, ~(13)C and ~(17)O labeled samples) indicate formation of an Fe-C-H containing organometallic intermediate, most likely a ferraoxetane. This is then rapidly reduced to a ferracyclopropane in which the HMBPP product forms an η~2-alkenyl π- (or π/σ) complex with the 4th Fe in the Fe_4S_4 cluster, and a similar "metallacycle" also forms between isopentenyl diphosphate (IPP) and GcpE. Based on this metallacycle concept, we show that an alkyne (propargyl) diphosphate is a good (K_i ～ 300 nM) GcpE inhibitor, and supported again by EPR and ENDOR results (a ~(13)C hyperfine coupling of ～7 MHz), as well as literature precedent, we propose that the alkyne forms another π/σ metallacycle, an η~2-alkynyl, or ferracyclo-propene. Overall, the results are of broad general interest because they provide new mechanistic insights into GcpE catalysis and inhibition, with organometallic bond formation playing, in both cases, a key role.