Lagrange Magali, Charbonnier Sebastian, Orfanoudakis Georges, Robinson Philip, Zanier Katia, Masson Murielle, Lutz Yves, Trave Gilles, Weiss Etienne, Deryckere François
UMR7100, Ecole Supérieure de Biotechnologie de Strasbourg, Pole API, boulevard Sébastien Brant, 67412 Illkirch Cedex, France.
IGBMC, CNRS/INSERM/ULP, 1 rue Laurent Fries, BP 10142, 67404 Illkirch Cedex, France.
J Gen Virol. 2005 Apr;86(Pt 4):1001-1007. doi: 10.1099/vir.0.80607-0.
The E6 protein of cancer-associated human papillomavirus type 16 (16E6) binds to p53 and, in association with E6AP, promotes its degradation through the ubiquitin-proteasome pathway. The aim of this work was to develop monoclonal antibodies against 16E6 and to test their effect on the binding of 16E6 to p53 and E6AP, and on the degradation of p53. It was shown that an antibody directed against the N terminus of 16E6 inhibited E6AP-dependent binding to p53 and degradation of p53, whereas two different antibodies directed to the second zinc-binding domain of 16E6 reduced 16E6 E6AP-independent binding to p53 and binding to E6AP but not degradation of p53.
癌相关的人乳头瘤病毒16型(16E6)的E6蛋白与p53结合,并与E6AP一起,通过泛素-蛋白酶体途径促进其降解。这项工作的目的是开发针对16E6的单克隆抗体,并测试它们对16E6与p53和E6AP结合的影响,以及对p53降解的影响。结果表明,一种针对16E6 N端的抗体抑制了E6AP依赖的与p53的结合以及p53的降解,而两种针对16E6第二个锌结合结构域的不同抗体减少了16E6不依赖E6AP与p53的结合以及与E6AP的结合,但没有减少p53的降解。