Chavez L G, Scherage H A
Biochemistry. 1977 May 3;16(9):1849-56. doi: 10.1021/bi00628a014.
An immunological method is used to follow the folding of different portions of the reduced bovine pancreatic ribonuclease molecule during air oxidation. Antibodies that react specifically with segments 1-13, 31-79, and 80-124 of native ribonuclease, as they are folded, were purified by affinity chromatography, using antiserum to native ribonuclease and columns to which the ribonuclease fragments were attached. The kinetics of reaction between these prufied antibodies and refolded portions that are produced when reduced rebonuclease is oxidized by air demonstrate the presence of intermediate states of folding, and are consistent with folding of the anti-genic determinants in the order 80-124, 1-13, and 31-79. The relative stabilities of each of these segments to thermal denaturation in the native protein provide additional evidence that the native conformation of region 80-124 is a very stable one in the intact molecule. On the basis of these two types of evidence, it appears that segment 80-124 contains a nucleation site for the folding of the protein molecule.
一种免疫学方法被用于追踪还原型牛胰核糖核酸酶分子在空气氧化过程中不同部分的折叠情况。当天然核糖核酸酶的片段1 - 13、31 - 79和80 - 124折叠时,能与它们特异性反应的抗体通过亲和层析进行纯化,该方法使用针对天然核糖核酸酶的抗血清以及连接有核糖核酸酶片段的柱子。这些纯化后的抗体与还原型核糖核酸酶被空气氧化时产生的重新折叠部分之间的反应动力学证明了折叠中间态的存在,并且与抗原决定簇按80 - 124、1 - 13和31 - 79的顺序折叠相一致。这些片段在天然蛋白质中对热变性的相对稳定性提供了额外证据,表明在完整分子中80 - 124区域的天然构象非常稳定。基于这两类证据,似乎80 - 124片段包含蛋白质分子折叠的一个成核位点。