Development of Small Molecular Proteasome Inhibitors Using aCaenorhabditis elegansScreen

[摘要] We have developed a screening protocol to identify compounds with characteristics of small molecule proteasome inhibitors using the real-time analysis of theCaenorhabditis elegansgerm line.This screen is able to identify compounds that induce germ line phenotypes characteristic of a reduction in proteasome function such as changes in polarity, aberrant nuclear morphology, and stimulation of apoptosis. This basic protocol is amenable to a high throughput (96-well) format and has been used successfully to identify multiple compounds for further analysis based on structural elements from the naturally occurring compounds lactacystin and theβ-lactone homologs omuralide and salinosporamide A. The further development of this assay system should allow for the generation of novel small molecule proteasome inhibitors in a genetically tractable whole animal amenable to biochemical analysis.

[学科分类] 药学