Kessler F, Blobel G
Laboratory of Cell Biology, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10021, USA.
Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7684-9. doi: 10.1073/pnas.93.15.7684.
We report the molecular cloning of import intermediate associated protein (IAP) 100, a 100-kDa protein of the chloroplast protein import machinery of peas. IAP100 contains two potential alpha-helical transmembrane segments and also behaves like an integral membrane protein. It was localized to the inner chloroplast envelope membrane. Immunoprecipitation experiments using monospecific anti-IAP100 antibodies and a nonionic detergent-generated chloroplast lysate gave the following results. (i) The four integral membrane proteins of the outer chloroplast import machinery were not coprecipitated with IAP100 indicating that the inner and outer membrane import machineries are not coupled in isolated chloroplasts. (ii) the major protein that coprecipitated with IAP100 was identified as stromal chaperonin 60 (cpn60); the association of IAP100 and cpn60 was specific and was abolished when immunoprecipitation was carried out in the presence of ATP. (iii) In a lysate from chloroplasts that had been preincubated for various lengths of time in an import reaction with radiolabeled precursor (pS) of the small subunit of Rubisco, we detected coimmunoprecipitation of IAP100, cpn60, and the imported mature form (S) of precursor. Relative to the time course of import, coprecipitation of S first increased and then decreased, consistent with a transient association of the newly imported S with the chaperonin bound to IAP100. These data suggest that IAP100 serves in recruiting chaperonin for folding of newly imported proteins.
我们报道了输入中间相关蛋白(IAP)100的分子克隆,它是豌豆叶绿体蛋白输入机制中的一种100 kDa蛋白。IAP100包含两个潜在的α - 螺旋跨膜片段,并且表现得像一种整合膜蛋白。它定位于叶绿体内膜。使用单特异性抗IAP100抗体和非离子去污剂处理产生的叶绿体裂解物进行免疫沉淀实验,得到了以下结果。(i)叶绿体外部输入机制的四种整合膜蛋白没有与IAP100共沉淀,这表明在分离的叶绿体中内膜和外膜输入机制没有耦合。(ii)与IAP100共沉淀的主要蛋白被鉴定为基质伴侣蛋白60(cpn60);IAP100和cpn60的结合是特异性的,并且在ATP存在下进行免疫沉淀时这种结合被消除。(iii)在与放射性标记的核酮糖-1,5-二磷酸羧化酶小亚基前体(pS)进行输入反应中预孵育了不同时长的叶绿体裂解物中,我们检测到IAP100、cpn60和前体的输入成熟形式(S)的共免疫沉淀。相对于输入的时间进程,S的共沉淀先增加然后减少,这与新输入的S与结合到IAP100的伴侣蛋白的短暂结合一致。这些数据表明IAP100在招募伴侣蛋白以折叠新输入的蛋白质方面发挥作用。