The thylakoid membrane protein ALB3 associates with the cpSecY-translocase in Arabidopsis thaliana

被引:64
作者
Klostermann, E
Helling, ID
Carde, JP
Schünemann, D
机构
[1] Rhein Westfal TH Aachen, Inst Biol 3, D-52074 Aachen, Germany
[2] Univ Bordeaux, F-33883 Villenave Dornon, France
关键词
chloroplast; light-harvesting chlorophyll protein (LHCP); protein-protein interaction; protein translocation;
D O I
10.1042/BJ20021291
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The integration of light-harvesting chlorophyll proteins (LHCPs) into the thylakoid membrane requires the integral thylakoid membrane protein ALB3, a homologue of the bacterial cytoplasmic membrane protein YidC. In bacteria, YidC is associated with the SecY-translocase and facilitates the integration of Sec-dependent proteins into the plasma membrane. In addition, it is also involved in the insertion of Sec-independent proteins. In the present study we demonstrate, in Arabidopsis thaliana, that most ALB3 is a constituent of an oligomeric complex of approx. 180 kDa. In addition, we detected ALB3 in several higher-molecular-mass complexes (up to 700 kDa). Furthermore, we show that most ALB3 co-fractionates with cpSecY during gel-filtration analysis and blue native gel electrophoresis, suggesting an association of ALB3 with the cpSecY complex. A direct interaction of ALB3 with the cpSecY complex was demonstrated by co-immunoprecipitation experiments using digitonin-solubilized thylakoid membrane proteins and anti-cpSecY or anti-ALB3 antibodies. This result was further confirmed by electron microscopic co-immunolocalization of ALB3 and cpSecY. In addition, an association of ALB3 with the cpSecY complex was demonstrated directly by cross-linking experiments using the chemical crosslinker disuccinimidyl suberate.
引用
收藏
页码:777 / 781
页数:5
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