Journal article
A crystallographic investigation of phosphoantigen binding to isopentenyl pyrophosphate/dimethylallyl pyrophosphate isomerase
Journal of the American Chemical Society, Vol.127(2), pp.536-537
01/19/2005
DOI: 10.1021/ja040207i
PMID: 15643873
Abstract
We report the crystallographic structures of the potent phosphoantigens Phosphostim (the bromohydrin of isopentenyl pyrophosphate) and E-4-hydroxy-3-methyl-but-2-enyl pyrophosphate bound to the mevalonate pathway enzyme isopentenyl pyrophosphate/dimethylallyl pyrophosphate isomerase (IPPI). Racemic Phosphostim forms covalent complexes with IPPI: a 4-thioether with C67 and a 4-ester with E116. Only the E116 ester forms with the chiral species, S-Phosphostim, with the w.t. enzyme, while the C67 thioether forms with a mutant Y104F IPPI. The potent phosphoantigen HMBPP also binds to IPPI, but is only a weak ( approximately 50 muM) inhibitor. These results strongly support an SN2 reaction for inhibition of IPPI by Phosphostim, in contrast to the SN1 or concerted type of reaction found with epoxide inhibitors, which react at C-3, and are of general interest in the context of the development of novel mevalonate pathway inhibitors. They also provide clues as to the nature of the binding site of synthetic phosphoantigens in gammadelta T cell activation. In particular, both bromohydrin and epoxy phosphoantigens are potent, irreversible inhibitors of IPPI while HMBPP is only a weak inhibitor, ruling out an IPPI or IPPI-like target for HMBPP in gammadelta T cell activation.
Details
- Title: Subtitle
- A crystallographic investigation of phosphoantigen binding to isopentenyl pyrophosphate/dimethylallyl pyrophosphate isomerase
- Creators
- Johan Wouters - Institute de Recherche Wiame and Laboratoire de Microbiologie, Universite Libre de Bruxelles, 1 Avenue E. Gryson, 1070 Bruxelles, BelgiumFenglin YinYongcheng SongYonghui ZhangYamina OudjamaVictor StalonLouis DroogmansCraig T MoritaEric Oldfield
- Resource Type
- Journal article
- Publication Details
- Journal of the American Chemical Society, Vol.127(2), pp.536-537
- DOI
- 10.1021/ja040207i
- PMID
- 15643873
- ISSN
- 0002-7863
- eISSN
- 1520-5126
- Grant note
- EB00271 / NIBIB NIH HHS AR045504 / NIAMS NIH HHS GM50694 / NIGMS NIH HHS
- Language
- English
- Date published
- 01/19/2005
- Academic Unit
- Internal Medicine
- Record Identifier
- 9984094754302771
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