Terao K, Uchiumi T, Kobayashi Y, Ogata K
Biochim Biophys Acta. 1980 Jan 24;621(1):72-82. doi: 10.1016/0005-2795(80)90063-x.
(1) The 40-S ribosomal subunits of rat liver were treated with a bifunctional cross-linking reagent, dimethyl suberimidate. Cross-linked protein-protein dimers were separated by two-dimensional acrylamide gel electrophoresis. The stained cross-linked complexes within the gel were radioiodinated without the elution of proteins from the gel and were cloven into the original monomeric protein constituents by ammonolysis. The proteins in each dimer were finally identified by two-dimensional acrylamide gel electrophoresis of the cloven monomeric proteins, followed by radioautography of the stained gel. (2) The molecular weights of cross-linked complexes were determined by SDS-polyacrylamide gel electrophoresis and were compared with those of their constituent proteins. (3) The following dimers were proposed from these results: S3-S12 (S3 or S3a-S11), S4-S12 (S3b-S11, S5-S7 (S4-S6), S5-S22 (S4-S23 or S24), S6-S8 (S5-S7), S8-S16 (S7-S18), S17-S21 (S16--S19) and S22A-S22B (S23-S24), designated according to our numbering system [1]. The designations according to the proposed uniform nomenclature [2] are described in parentheses.
(1) 用双功能交联剂辛二酰亚胺二甲酯处理大鼠肝脏的40-S核糖体亚基。通过二维丙烯酰胺凝胶电泳分离交联的蛋白质-蛋白质二聚体。凝胶内染色的交联复合物在不将蛋白质从凝胶上洗脱的情况下进行放射性碘化,然后通过氨解裂解成原来的单体蛋白质成分。通过对裂解后的单体蛋白质进行二维丙烯酰胺凝胶电泳,随后对染色凝胶进行放射自显影,最终鉴定每个二聚体中的蛋白质。(2) 通过SDS-聚丙烯酰胺凝胶电泳测定交联复合物的分子量,并与其组成蛋白质的分子量进行比较。(3) 根据这些结果提出了以下二聚体:S3-S12(S3或S3a-S11)、S4-S12(S3b-S11)、S5-S7(S4-S6)、S5-S22(S4-S23或S24)、S6-S8(S5-S7)、S8-S16(S7-S18)、S17-S21(S16-S19)和S22A-S22B(S23-S24),按照我们的编号系统[1]命名。括号中为根据提议的统一命名法[2]的名称。