Abstract
p8 and prothymosin α are two natively unstructured proteins with anti-apoptotic activity. We showed that their interaction results in the formation of a one-to-one heterodimer complex with stable structure. To test whether the heterodimer bears the function previously attributed to both proteins, we monitored the consequences on apoptosis of modulating in vitro the concentrations of both proteins. Overexpression was obtained by transfection of appropriate vectors and inhibition by using specific siRNAs. In all conditions inhibition of apoptosis correlated with the level of the partner with lowest concentration, demonstrating that the anti-apoptotic effect previously attributed to each proteins was in fact borne by the p8/ProTα complex, the two proteins, being individually inactive. These results show that the function attributed to a natively unfolded protein might actually belong to a multi-protein complex in which the protein of interest is engaged. ©2006 Landes Bioscience.
Author supplied keywords
Cite
CITATION STYLE
Malicet, C., Dagorn, J. C., Neira, J. L., & Iovanna, J. L. (2006, April 15). p8 and prothymosin alpha: Unity is strength. Cell Cycle. Taylor and Francis Inc. https://doi.org/10.4161/cc.5.8.2686
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.