Ludwig-Maximilians-Universität München, Department Biologie I, Plant Biochemistry, Grosshaderner Strasse 2-4, Planegg-Martinsried, Germany.
BMC Plant Biol. 2011 Sep 30;11:133. doi: 10.1186/1471-2229-11-133.
The Tic complex (Translocon at the inner envelope membrane of chloroplasts) mediates the translocation of nuclear encoded chloroplast proteins across the inner envelope membrane. Tic110 forms one prominent protein translocation channel. Additionally, Tic20, another subunit of the complex, was proposed to form a protein import channel - either together with or independent of Tic110. However, no experimental evidence for Tic20 channel activity has been provided so far.
We performed a comprehensive biochemical and electrophysiological study to characterize Tic20 in more detail and to gain a deeper insight into its potential role in protein import into chloroplasts. Firstly, we compared transcript and protein levels of Tic20 and Tic110 in both Pisum sativum and Arabidopsis thaliana. We found the Tic20 protein to be generally less abundant, which was particularly pronounced in Arabidopsis. Secondly, we demonstrated that Tic20 forms a complex larger than 700 kilodalton in the inner envelope membrane, which is clearly separate from Tic110, migrating as a dimer at about 250 kilodalton. Thirdly, we defined the topology of Tic20 in the inner envelope, and found its N- and C-termini to be oriented towards the stromal side. Finally, we successfully reconstituted overexpressed and purified full-length Tic20 into liposomes. Using these Tic20-proteoliposomes, we could demonstrate for the first time that Tic20 can independently form a cation selective channel in vitro.
The presented data provide first biochemical evidence to the notion that Tic20 can act as a channel protein within the chloroplast import translocon complex. However, the very low abundance of Tic20 in the inner envelope membranes indicates that it cannot form a major protein translocation channel. Furthermore, the independent complex formation of Tic20 and Tic110 argues against a joint channel formation. Thus, based on the observed channel activity of Tic20 in proteoliposomes, we speculate that the chloroplast inner envelope contains multiple (at least two) translocation channels: Tic110 as the general translocation pore, whereas Tic20 could be responsible for translocation of a special subset of proteins.
Tic 复合物(叶绿体内膜转位体)介导核编码的叶绿体蛋白穿过内膜的转运。Tic110 形成一个突出的蛋白转运通道。此外,复合物的另一个亚基 Tic20 被提议形成一个蛋白导入通道 - 要么与 Tic110 一起,要么独立于 Tic110。然而,目前还没有提供 Tic20 通道活性的实验证据。
我们进行了全面的生化和电生理学研究,以更详细地描述 Tic20,并更深入地了解其在叶绿体蛋白导入中的潜在作用。首先,我们比较了豌豆和拟南芥中 Tic20 和 Tic110 的转录本和蛋白水平。我们发现 Tic20 蛋白通常不太丰富,在拟南芥中尤为明显。其次,我们证明 Tic20 在内膜中形成一个大于 700 千道尔顿的复合物,明显与 Tic110 分开,以约 250 千道尔顿的二聚体形式迁移。第三,我们确定了 Tic20 在内膜中的拓扑结构,发现其 N 和 C 末端朝向基质侧。最后,我们成功地将过表达和纯化的全长 Tic20 重新组装到脂质体中。使用这些 Tic20-脂囊泡,我们首次证明 Tic20 可以在体外独立形成阳离子选择性通道。
所提供的数据首次提供了生化证据,证明 Tic20 可以作为叶绿体导入转位体复合物中的通道蛋白发挥作用。然而,Tic20 在内膜中的极低丰度表明它不能形成主要的蛋白转运通道。此外,Tic20 和 Tic110 的独立复合物形成反对联合通道形成。因此,基于在脂囊泡中观察到的 Tic20 通道活性,我们推测叶绿体内膜包含多个(至少两个)转运通道:Tic110 作为一般转运孔,而 Tic20 可能负责特殊蛋白质亚群的转运。