Fane B, Villafane R, Mitraki A, King J
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
J Biol Chem. 1991 Jun 25;266(18):11640-8.
Suppressor mutations which alleviate the defects in folding mutants of the P22 gene 9 tailspike protein have recently been isolated (Fane, B. and King, J. (1991) Genetics 127, 263-277). The starting folding defects were in missense polypeptide chains generated by host amino acid insertions at different amber mutant sites. Fragments of genes carrying the amber mutations with and without their independently isolated suppressor mutations were cloned and sequenced. The parental nonsense mutations were located at Q45, K122, E156, W202, W207, Y232, and W365. Their conformational suppressors were single amino acid substitutions at a limited set of sites, V84 greater than A, V331 greater than A, and A334 greater than V. The V331 greater than A or A334 greater than V suppressors were independently recovered starting with different mutant sites suggesting that they acted by some global or general mechanism. When the V331 greater than A and A334 greater than V mutations were crossed into well-characterized temperature-sensitive folding (tsf) mutants at various sites in the tailspike protein, they suppressed all of the eight tsf mutants tested. Since the tsf defects destabilize folding intermediates rather than the native conformation, this result implies that the suppressors act in the folding pathway. Strains carrying the isolated suppressor mutations displayed no obvious phenotypic defect and formed native biologically active tailspikes. Thus, these single amino acid substitutions have striking influences on the efficiency of intracellular chain folding, without causing functional defects in the native protein.
最近分离出了抑制突变,这些突变可缓解P22基因9尾刺蛋白折叠突变体中的缺陷(法内,B.和金,J.(1991年)《遗传学》127卷,263 - 277页)。起始的折叠缺陷存在于宿主在不同琥珀突变位点插入氨基酸所产生的错义多肽链中。携带琥珀突变及其独立分离出的抑制突变的基因片段被克隆并测序。亲本无义突变位于Q45、K122、E156、W202、W207、Y232和W365。它们的构象抑制子是在一组有限位点上的单氨基酸替换,V84突变为A、V331突变为A以及A334突变为V。从不同突变位点开始独立获得了V331突变为A或A334突变为V的抑制子,这表明它们通过某种全局或通用机制起作用。当将V331突变为A和A334突变为V的突变引入尾刺蛋白不同位点特征明确的温度敏感折叠(tsf)突变体中时,它们抑制了所测试的所有八个tsf突变体。由于tsf缺陷使折叠中间体而非天然构象不稳定,这一结果意味着抑制子在折叠途径中起作用。携带分离出的抑制突变的菌株没有表现出明显的表型缺陷,并形成了天然的生物活性尾刺。因此,这些单氨基酸替换对细胞内链折叠效率有显著影响,而不会在天然蛋白中造成功能缺陷。