Synthesis and Enzymatic Phosphorylation of a Photoactivatable Dolichol Analogue

Diego Grassi, V. Lippuner, Markus Aebi, Josef Brunner, A. Vasella

Journal of the American Chemical Society · 1997 · 27 citations · 22 references

Concepts

Abstract

The synthesis of the photochemical probes 6 and 7 is described. These photoprobes are analogues of dolichol and dolichol phosphate, obligatory intermediates in the N -linked glycosylation pathway in the endoplasmic reticulum. The synthesis of 6 and 7 follows a new strategy. It involves the sequential alkylation of a monoterpenoid hydroxysulfonyl dianion with allyl chlorides. The photoreactive group, a 3-(trifluoromethyl)-3-aryldiazirine, was connected to the hydroxylated methyl group of the β-prenyl unit of the fully assembled polyprenyl chain. The photoactivatable dolichol analogue 6 is a substrate for dolichol kinase from yeast membranes, an essential enzyme involved in the N -linked glycosylation pathway.

References

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