Synthesis and Effect of Nonhydrolyzable Xanthosine Triphosphate Derivatives on Prenylation of Rab5D136N
- 1Department of Pharmacology and Molecular Toxicology, University of Massachusetts Medical School, Worcester, Massachusetts 01655 (I.Y., G.E.W.), and 2Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts 02115 (J.Y.P., M.W.-R.)
Abstract
A novel and convenient method for nucleoside triphosphate synthesis was applied to the preparation of potentially nonhydrolyzable xanthosine triphosphate derivatives. The N-methylimidazolide of xanthosine 5′-monophosphate reacted rapidly with methylenediphosphonic acid and imidodiphosphonic acid to give xanthosine 5′-(β,γ-methylene)triphosphate and xanthosine 5′-(β,γ-imido)triphosphate, respectively, in good yields. Both compounds inhibited the xanthosine-diphosphate-dependent prenylation of a mutant of Rab5, Rab5D136N, the nucleotide specificity of which had been converted from GTP to xanthosine triphosphate. The results indicate that xanthosine 5′-(β,γ-methylene)triphosphate and xanthosine 5′-(β,γ-imido)triphosphate bound to the mutant protein with similar affinities and were not hydrolyzed under the assay conditions. These novel derivatives may be useful tools for the study of the role of individual GTPases mutated to xanthosine triphosphate specificity in the background of other GTP-binding proteins.
Footnotes
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Send reprint requests to: George E. Wright, Ph.D., Department of Pharmacology and Molecular Toxicology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655. E-mail: wright{at}icarus.ummed.edu
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This work was supported by American Cancer Society Research Grant CB-15 to M.W.-R., who is an established investigator of the American Heart Association.
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I. Y. and J. Y. P. contributed equally to this article.
- Abbreviations:
- XDP
- xanthosine diphosphate
- XMPPCH2P
- xanthosine 5′-(β,γ-methylene)triphosphate
- XMPPNHP
- xanthosine 5′-(β,γ-imido)triphosphate
- XMP
- xanthosine monophosphate
- XTP
- xanthosine triphosphate
- TEAB
- triethylammonium bicarbonate buffer
- DMF
- N,N-dimethylformamide
- HR
- high-resolution
- FAB
- fast-atom bombardment
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- Received July 25, 1996.
- Accepted September 25, 1996.
- The American Society for Pharmacology and Experimental Therapeutics
