Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1938349 | Biochemical and Biophysical Research Communications | 2007 | 5 Pages |
Abstract
A primary cellular target of the clinical nitrogenous bisphosphonates is the isoprenoid biosynthetic pathway. Specifically these drugs inhibit the enzyme farnesyl pyrophosphate synthase and deplete cells of larger isoprenoids. Inhibition of this enzyme results in impaired processing of both farnesylated and geranylgeranylated proteins. We recently showed that isoprenoid-containing bisphosphonates such as digeranyl bisphosphonate inhibit protein geranylgeranylation and not farnesylation. Here, we show that this impairment results from potent and specific inhibition of geranylgeranyl pyrophosphate synthase, which leads to enhanced depletion of intracellular geranylgeranyl pyrophosphate relative to the nitrogenous bisphosphonate zoledronate.
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Authors
Andrew J. Wiemer, Huaxiang Tong, Kelly M. Swanson, Raymond J. Hohl,