Majima E, Koike H, Hong Y M, Shinohara Y, Terada H
Faculty of Pharmaceutical Sciences, University of Tokushima, Japan.
J Biol Chem. 1993 Oct 15;268(29):22181-7.
The effects of the membrane-impermeable fluorescent sulfhydryl reagent eosin 5-maleimide (EMA) and the membrane-permeable sulfhydryl reagent N-ethylmaleimide (NEM) on ADP transport via the ADP/ATP carrier and their labeling sites in the carrier were studied in bovine heart submitochondrial particles. Of the 4 cysteine residues in the carrier, EMA labeled Cys159 very rapidly, Cys56 slowly, and Cys256 very slowly and did not label Cys128. Its labeling of Cys159 was associated with inhibition of the ADP transport, suggesting that the peptide segment containing Cys159 is involved in the transport of adenine nucleotides. In contrast to the very rapid binding of EMA to Cys159, NEM bound to Cys56 more slowly and labeled Cys159 and Cys256 much more slowly. Like EMA, it did not react with Cys128. The labeling of Cys56 with NEM also inhibited ADP transport. From these results, the locations of these cysteine residues in the ADP/ATP carrier are discussed in relation to the transport of adenine nucleotides mediated by the ADP/ATP carrier.
在牛心亚线粒体颗粒中,研究了膜不可渗透的荧光巯基试剂 eosin 5-马来酰亚胺(EMA)和膜可渗透的巯基试剂 N-乙基马来酰亚胺(NEM)对通过 ADP/ATP 载体的 ADP 转运及其在载体中的标记位点的影响。在载体的 4 个半胱氨酸残基中,EMA 非常快速地标记 Cys159,缓慢标记 Cys56,非常缓慢地标记 Cys256,且不标记 Cys128。其对 Cys159 的标记与 ADP 转运的抑制相关,表明含有 Cys159 的肽段参与腺嘌呤核苷酸的转运。与 EMA 非常快速地结合到 Cys159 相反,NEM 与 Cys56 的结合更慢,标记 Cys159 和 Cys256 更慢得多。与 EMA 一样,它不与 Cys128 反应。NEM 对 Cys56 的标记也抑制了 ADP 转运。根据这些结果,结合由 ADP/ATP 载体介导的腺嘌呤核苷酸转运,讨论了这些半胱氨酸残基在 ADP/ATP 载体中的位置。