Montenarh M, Kohler M, Henning R
J Virol. 1986 Nov;60(2):761-4. doi: 10.1128/JVI.60.2.761-764.1986.
We investigated the formation of native complexes between simian virus 40 large T antigen and the cellular protein p53 (T-p53) by using simian virus 40 tsA58-transformed mouse fibroblasts (tsA58 F2b). We observed that newly synthesized p53 bound to all structural subclasses of large T antigen detectable on sucrose density gradients. This led to various intermediates of T-p53 complexes which converted within 2 h into typical mature aggregates. The final levels of stable T-p53 complexes seemed to be determined by p53 rather than by large T antigen.
我们利用猿猴病毒40 tsA58转化的小鼠成纤维细胞(tsA58 F2b)研究了猿猴病毒40大T抗原与细胞蛋白p53(T-p53)之间天然复合物的形成。我们观察到,新合成的p53与在蔗糖密度梯度上可检测到的大T抗原的所有结构亚类结合。这导致了T-p53复合物的各种中间体,它们在2小时内转化为典型的成熟聚集体。稳定的T-p53复合物的最终水平似乎由p53而非大T抗原决定。