Development Center of Plant Germplasm Resources, College of Life Sciences, Shanghai Normal University, Shanghai, 200234, China.
Shanghai Key Laboratory of Plant Molecular Sciences, College of Life Sciences, Shanghai Normal University, Shanghai, 200234, China.
Nat Commun. 2024 Apr 10;15(1):3122. doi: 10.1038/s41467-024-46863-y.
In chloroplasts, insertion of proteins with multiple transmembrane domains (TMDs) into thylakoid membranes usually occurs in a co-translational manner. Here, we have characterized a thylakoid protein designated FPB1 (Facilitator of PsbB biogenesis1) which together with a previously reported factor PAM68 (Photosynthesis Affected Mutant68) is involved in assisting the biogenesis of CP47, a subunit of the Photosystem II (PSII) core. Analysis by ribosome profiling reveals increased ribosome stalling when the last TMD segment of CP47 emerges from the ribosomal tunnel in fpb1 and pam68. FPB1 interacts with PAM68 and both proteins coimmunoprecipitate with SecY/E and Alb3 as well as with some ribosomal components. Thus, our data indicate that, in coordination with the SecY/E translocon and the Alb3 integrase, FPB1 synergistically cooperates with PAM68 to facilitate the co-translational integration of the last two CP47 TMDs and the large loop between them into thylakoids and the PSII core complex.
在叶绿体中,具有多个跨膜结构域(TMD)的蛋白质插入类囊体膜通常以共翻译的方式发生。在这里,我们对一种被命名为 FPB1(PsbB 生物发生 1 的促进因子)的类囊体蛋白进行了表征,该蛋白与之前报道的因子 PAM68(光合作用受影响突变体 68)一起参与辅助 CP47 的生物发生,CP47 是光系统 II(PSII)核心的一个亚基。核糖体图谱分析显示,当 CP47 的最后一个 TMD 片段从核糖体隧道中出现时,fpb1 和 pam68 中的核糖体停滞增加。FPB1 与 PAM68 相互作用,这两种蛋白质都与 SecY/E 和 Alb3 以及一些核糖体成分共免疫沉淀。因此,我们的数据表明,FPB1 与 SecY/E 转运体和 Alb3 整合酶协调合作,协同 PAM68 促进最后两个 CP47 TMD 及其之间的大环共翻译整合到类囊体和 PSII 核心复合物中。