Chen D, Schnell D J
Department of Biological Sciences, Rutgers, The State University of New Jersey, Newark, New Jersey 07102, USA.
J Biol Chem. 1997 Mar 7;272(10):6614-20. doi: 10.1074/jbc.272.10.6614.
IAP34 is a 34-kDa component of the outer membrane complex that mediates the initial stages of protein import into chloroplasts (Seedorf, M., Waegemann, K., and Soll, J. (1995) Plant J. 7, 401-411; Kessler, F., Blobel, G., Patel, H. A., and Schnell, D. J. (1994) Science 266, 1035-1039). We have investigated the targeting and insertion of IAP34 at the outer envelope membrane. The analyses of IAP34 deletion mutants and hybrid proteins (consisting of regions of IAP34 fused to the soluble IgG-binding domain of staphylococcal protein A) suggest that the transmembrane domain and C-terminal tail of IAP34 contain information essential but not sufficient for targeting to the outer membrane. Treatment of chloroplasts with exogenous proteases does not affect IAP34 insertion, indicating that targeting does not require surface-exposed receptors at the envelope. GTP or GDP is required for maximal integration of IAP34 into the outer membrane. The GTP/GDP requirement is attributed to the intrinsic GTP binding activity of IAP34 because GTP/GDP binding-deficient mutants are defective in outer membrane insertion. On the basis of these observations, we propose that IAP34 is targeted to the chloroplast by a C-terminal signal and efficiently integrated into the outer membrane by conformation-induced insertion upon GTP/GDP binding.
IAP34是外膜复合物的一个34千道尔顿的组分,它介导蛋白质导入叶绿体的初始阶段(Seedorf, M., Waegemann, K., and Soll, J. (1995) Plant J. 7, 401 - 411; Kessler, F., Blobel, G., Patel, H. A., and Schnell, D. J. (1994) Science 266, 1035 - 1039)。我们研究了IAP34在外膜的靶向和插入过程。对IAP34缺失突变体和杂交蛋白(由IAP34的区域与葡萄球菌蛋白A的可溶性IgG结合结构域融合而成)的分析表明,IAP34的跨膜结构域和C末端尾巴包含靶向到外膜所必需但不充分的信息。用外源蛋白酶处理叶绿体不会影响IAP34的插入,这表明靶向不需要包膜上表面暴露的受体。IAP34最大程度地整合到外膜需要GTP或GDP。对GTP/GDP的需求归因于IAP34固有的GTP结合活性,因为GTP/GDP结合缺陷型突变体在外膜插入方面存在缺陷。基于这些观察结果,我们提出IAP34通过C末端信号靶向到叶绿体,并在结合GTP/GDP时通过构象诱导插入有效地整合到外膜中。