Gillespie L L
J Biol Chem. 1987 Jun 15;262(17):7939-42.
Chemical cross-linking procedures have been employed to study possible interactions between components of the mitochondrial outer membrane and NH2-terminal signal sequences located in proteins destined for import into the organelle. A synthetic peptide comprising amino acids 1-27 of pre-ornithine carbamyltransferase (pOCT) was found to interact specifically with a mitochondrial polypeptide of apparent molecular size 30 kDa. Membrane fractionation and protease accessibility analyses indicated that the polypeptide, designated p30, is located in the outer membrane. Binding of the synthetic peptide to p30 was saturable and reversible; Scatchard analysis of the binding data revealed a dissociation constant of 2 X 10(-6) M and predicts that p30 constitutes 4-10% of the outer mitochondrial membrane protein. Mild trypsin digestion of the mitochondrial surface destroyed both the ability of p30 to cross-link to the signal peptide and the ability of the organelle to import pOCT. Neither parameter was affected, however, by pretreatment of mitochondria with 1 M KCl.
化学交联程序已被用于研究线粒体外膜成分与位于注定要导入该细胞器的蛋白质中的氨基末端信号序列之间可能的相互作用。发现一种包含鸟氨酸氨甲酰转移酶前体(pOCT)第1 - 27位氨基酸的合成肽与一种表观分子大小为30 kDa的线粒体多肽特异性相互作用。膜分级分离和蛋白酶可及性分析表明,该多肽命名为p30,位于外膜。合成肽与p30的结合是可饱和且可逆的;对结合数据的Scatchard分析显示解离常数为2×10⁻⁶ M,并预测p30占线粒体外膜蛋白的4 - 10%。对线粒体表面进行温和的胰蛋白酶消化会破坏p30与信号肽交联的能力以及该细胞器导入pOCT的能力。然而,用1 M KCl预处理线粒体对这两个参数均无影响。