Breese K, Friedrich T, Figge J
Department of Microbiology, Immunology & Molecular Genetics, Albany Medical College, New York 12208.
In Vitro Cell Dev Biol Anim. 1993 Dec;29A(12):952-5. doi: 10.1007/BF02634234.
Simian virus 40 (SV40) large T antigen (T), a potent dominant oncogene product, forms a specific complex with the human retinoblastoma protein (pRb), a cellular growth suppressor. We have used a recombinant pRb fusion protein (GST-Rb) in combination with extracts from a line of SV40-transformed human lung cells (WI-26 VA4) to develop a simple, non-radioactive assay to rapidly screen for competitive inhibitors of T/pRb binding. We illustrate the use of the assay by demonstrating that several short peptides containing the signature sequence, Leu-X-Cys-X-Glu, can inhibit T/pRb complex formation. In contrast, peptides containing the related motif, Leu-X-Glu-X-Glu, including two peptides derived from the transcription factor E2F, are inactive in this assay. These results show that Glu cannot substitute for Cys in the Leu-X-Cys-X-Glu motif. This assay will facilitate the identification of agents that are inhibitors of T/pRb complex formation and that might exert effects on cellular growth regulation.
猴病毒40(SV40)大T抗原(T)是一种强大的显性癌基因产物,可与细胞生长抑制因子人视网膜母细胞瘤蛋白(pRb)形成特异性复合物。我们使用重组pRb融合蛋白(GST-Rb)与一株SV40转化的人肺细胞(WI-26 VA4)的提取物相结合,开发了一种简单的非放射性检测方法,用于快速筛选T/pRb结合的竞争性抑制剂。我们通过证明几种含有特征序列Leu-X-Cys-X-Glu的短肽可以抑制T/pRb复合物的形成来说明该检测方法的用途。相比之下,含有相关基序Leu-X-Glu-X-Glu的肽,包括两种源自转录因子E2F的肽,在该检测中无活性。这些结果表明,在Leu-X-Cys-X-Glu基序中,Glu不能替代Cys。该检测将有助于鉴定作为T/pRb复合物形成抑制剂且可能对细胞生长调节产生影响的试剂。