Subramanian A R, Rienhardt P, Kimura M, Suryanarayana T
Eur J Biochem. 1981 Oct;119(2):245-9. doi: 10.1111/j.1432-1033.1981.tb05600.x.
Escherichia coli ribosomal protein S1 and its mutant, shorter, form m1-S1 were cleaved at internal methionyl residues to yield, respectively, six and five fragments of Mr ranging from 1000 to 24000. Methods are described to isolate the fragments in pure form. Four of the fragments (designated F2a, F2b, F3 and F4) contain between 86 and 215 amino acids and are therefore as large as other ribosomal proteins. Fragment F2a, derived from the N-terminal region, has previously been shown to contain the major ribosome binding domain of S1 [S. Giorginis and A. R. Subramanian (1980) J. Mol. Biol. 141, 393--408]. Here we show that the RNA binding domain of S1 is essentially contained in F3 derived from the middle region of S1 and carrying the nonreactive--SH group. The reactive--SH group of S1, whose activity is modified by ligand binding, was localized in F2b, a fragment with little RNA binding capacity. The characteristic RNA binding domain and a weak ribosome binding domain of S1 have previously been localized in the large trypsin-resistent core S1-F1 [T. Suryanarayana and A. R. Subramanian (1979) J. Mol. Biol. 127, 41--54]. Together these data indicate that two of the key functional domain of S1 are located in two regions of the molecule separated by an open, exposed segment. The present study also revealed that the nonreactive--SH group of S1 becomes reactive in m1-S1 by the loss of the remote C-terminal region in the latter.
大肠杆菌核糖体蛋白S1及其较短的突变体m1-S1在内部甲硫氨酰残基处被切割,分别产生了6个和5个分子量在1000至24000之间的片段。文中描述了以纯形式分离这些片段的方法。其中4个片段(命名为F2a、F2b、F3和F4)包含86至215个氨基酸,因此与其他核糖体蛋白一样大。源自N端区域的片段F2a先前已被证明包含S1的主要核糖体结合结构域[S. Giorginis和A. R. Subramanian(1980年)《分子生物学杂志》141卷,393 - 408页]。在此我们表明,S1的RNA结合结构域基本上包含在源自S1中间区域且带有非反应性-SH基团的F3中。S1的反应性-SH基团,其活性因配体结合而改变,定位于F2b中,F2b是一个几乎没有RNA结合能力的片段。S1的特征性RNA结合结构域和较弱的核糖体结合结构域先前已定位于大的抗胰蛋白酶核心S1-F1中[T. Suryanarayana和A. R. Subramanian(1979年)《分子生物学杂志》127卷,41 - 54页]。这些数据共同表明,S1的两个关键功能结构域位于分子的两个区域,中间由一个开放的暴露片段隔开。本研究还表明,S1的非反应性-SH基团在m1-S1中由于后者远端C端区域的缺失而变得具有反应性。