Uncovering the Protein Translocon at the Chloroplast Inner Envelope Membrane

被引:285
作者
Kikuchi, Shingo [1 ]
Bedard, Jocelyn [1 ]
Hirano, Minako [2 ]
Hirabayashi, Yoshino [1 ]
Oishi, Maya [1 ]
Imai, Midori [1 ]
Takase, Mai [1 ]
Ide, Toru [2 ]
Nakai, Masato [1 ]
机构
[1] Osaka Univ, Inst Prot Res, Lab Regulat Biol React, Suita, Osaka 5650871, Japan
[2] Grad Sch Creat New Photon Ind, Nishi Ku, Hamamatsu, Shizuoka 4311202, Japan
基金
日本学术振兴会;
关键词
IMPORT MACHINERY; IN-VIVO; TIC20; CHANNEL; ARABIDOPSIS; FORMS; BIOGENESIS; COMPONENTS; APPARATUS; COMPLEX;
D O I
10.1126/science.1229262
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chloroplasts require protein translocons at the outer and inner envelope membranes, termed TOC and TIC, respectively, to import thousands of cytoplasmically synthesized preproteins. However, the molecular identity of the TIC translocon remains controversial. Tic20 forms a 1-megadalton complex at the inner membrane and directly interacts with translocating preproteins. We purified the 1-megadalton complex from Arabidopsis, comprising Tic20 and three other essential components, one of which is encoded by the enigmatic open reading frame ycf1 in the chloroplast genome. All four components, together with well-known TOC components, were found stoichiometrically associated with different translocating preproteins. When reconstituted into planar lipid bilayers, the purified complex formed a preprotein-sensitive channel. Thus, this complex constitutes a general TIC translocon.
引用
收藏
页码:571 / 574
页数:4
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