Burstein Y, Schechter I
Proc Natl Acad Sci U S A. 1977 Feb;74(2):716-20. doi: 10.1073/pnas.74.2.716.
The mRNA molecules coding for mouse immunoglobulin light (L) chains direct the cell-free synthesis of precursors in which extra peptide segments precede the amino termini of the mature proteins. The results of amino acid sequence analyses of two precursors labeled with 20 radioactive amino acids enabled unambiguous determination of the complete primary structure of the extra piece segments. The complete sequences (and sizes) of the NH2-terminal extra pieces are: in MOPC-104E lambda1 L-chain precursor, Met-Ala-Trp-Ile-Ser-Leu-Ile-Leu-Ser-Leu-Leu-Ala-Leu-Ser-Ser-Gly-Ala-Ile-Ser (19 residues); in MOPC-41 kappa L-chain precursor, Met-Asp-Met-Arg-Ala-Pro-Ala-Gln-Ile-Phe-Gly-Phe-Leu-Leu-Leu-Leu-Phe-Pro-Gly-Thr-Arg-Cys (22 residues). The extra pieces in the precursors of MOPC-104E (lambda1), MOPC-41 (kappa), and MOPC-321 (kappa) L-chains differ extensively from each other in their amino acid sequence (65-73%). In addition to this sequence heterogeneity, the extra pieces are characterized by a high percentage of hydrophobic residues: 69% in the MOPC-104E lambda1 L-chain precursor (this report), 73-75% in the kappa L-chain precursors [Schechter, I. & Burstein, Y. (1976) Proc, Natl. Acad. Sci. USA 73, 3273-3277]. The marked hydrophobicity of the extra piece suggests that it may favor interaction of the precursor with cell membranes, in a manner similar to the function of the "hydrophobic domain" of membrane-bound proteins. We propose two possible targets for interaction: (i) the endoplasmic membranes, where the NH2-terminal extra piece is cleaved from the precursor to yield mature protein destined for secretion; (ii) the cell surface membrane, where the intact precursor is anchored by virtue of the hydrophobic extra piece to serve as the antigen-recognizing receptor.
编码小鼠免疫球蛋白轻(L)链的mRNA分子指导无细胞体系中前体的合成,在这些前体中,额外的肽段位于成熟蛋白氨基末端之前。对用20种放射性氨基酸标记的两种前体进行氨基酸序列分析的结果,使得能够明确确定额外片段的完整一级结构。氨基末端额外片段的完整序列(及大小)如下:在MOPC-104E λ1 L链前体中,Met-Ala-Trp-Ile-Ser-Leu-Ile-Leu-Ser-Leu-Leu-Ala-Leu-Ser-Ser-Gly-Ala-Ile-Ser(19个残基);在MOPC-41 κ L链前体中,Met-Asp-Met-Arg-Ala-Pro-Ala-Gln-Ile-Phe-Gly-Phe-Leu-Leu-Leu-Leu-Phe-Pro-Gly-Thr-Arg-Cys(22个残基)。MOPC-104E(λ1)、MOPC-41(κ)和MOPC-321(κ)L链前体中的额外片段在氨基酸序列上彼此差异很大(65%-73%)。除了这种序列异质性外,额外片段的特征还在于疏水残基的比例很高:在MOPC-104E λ1 L链前体中为69%(本报告),在κ L链前体中为73%-75%[谢克特,I.和伯斯坦,Y.(1976年)《美国国家科学院院刊》73,3273-3277]。额外片段的显著疏水性表明,它可能以前体与细胞膜相互作用的方式,类似于膜结合蛋白“疏水结构域”的功能。我们提出了两个可能的相互作用靶点:(i)内质膜,氨基末端额外片段在此从前体上裂解下来,产生注定要分泌的成熟蛋白;(ii)细胞表面膜,完整的前体凭借疏水的额外片段锚定在其上,作为抗原识别受体。