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p8与前胸腺素α:团结就是力量。

p8 and prothymosin alpha: unity is strength.

作者信息

Malicet Cédric, Dagorn Jean Charles, Neira José Luis, Iovanna Juan L

机构信息

INSERM U.624, Stress Cellulaire, Marseille, France.

出版信息

Cell Cycle. 2006 Apr;5(8):829-30. doi: 10.4161/cc.5.8.2686. Epub 2006 Apr 17.

Abstract

p8 and prothymosin alpha 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/ProTalpha 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.

摘要

p8和原胸腺素α是两种具有抗凋亡活性的天然无结构蛋白。我们发现它们相互作用形成了一种结构稳定的一对一异源二聚体复合物。为了测试该异源二聚体是否具有先前赋予这两种蛋白的功能,我们监测了体外调节这两种蛋白浓度对细胞凋亡的影响。通过转染合适的载体实现过表达,并使用特异性小干扰RNA进行抑制。在所有条件下,细胞凋亡的抑制都与浓度最低的伙伴蛋白水平相关,这表明先前归因于每种蛋白的抗凋亡作用实际上由p8/原胸腺素α复合物承担,这两种蛋白单独时无活性。这些结果表明,归因于天然未折叠蛋白的功能实际上可能属于该蛋白所参与形成的多蛋白复合物。

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