Rottensteiner Hanspeter, Kramer Achim, Lorenzen Stephan, Stein Katharina, Landgraf Christiane, Volkmer-Engert Rudolf, Erdmann Ralf
Institut für Physiologische Chemie, Ruhr-Universität Bochum, 44780 Bochum, Germany.
Mol Biol Cell. 2004 Jul;15(7):3406-17. doi: 10.1091/mbc.e04-03-0188. Epub 2004 May 7.
Targeting of peroxisomal membrane proteins (PMPs) is a multistep process that requires not only recognition of PMPs in the cytosol but also their insertion into the peroxisomal membrane. As a consequence, targeting signals of PMPs (mPTS) are rather complex. A candidate protein for the PMP recognition event is Pex19p, which interacts with most PMPs. However, the respective Pex19p-binding sites are ill-defined and it is currently disputed whether these sites are contained within mPTS. By using synthetic peptide scans and yeast two-hybrid analyses, we determined and characterized Pex19p-binding sites in Pex11p and Pex13p, two PMPs from Saccharomyces cerevisiae. The sites turned out to be composed of a short helical motif with a minimal length of 11 amino acids. With the acquired data, it proved possible to predict and experimentally verify Pex19p-binding sites in several other PMPs by applying a pattern search and a prediction matrix. A peroxisomally targeted Pex13p fragment became mislocalized to the endoplasmic reticulum in the absence of its Pex19p-binding site. By adding the heterologous binding site of Pex11p, peroxisomal targeting of the Pex13p fragment was restored. We conclude that Pex19p-binding sites are well-defined entities that represent an essential part of the mPTS.
过氧化物酶体膜蛋白(PMPs)的靶向是一个多步骤过程,不仅需要在细胞质中识别PMPs,还需要将它们插入过氧化物酶体膜。因此,PMPs的靶向信号(mPTS)相当复杂。Pex19p是PMP识别事件的一个候选蛋白,它与大多数PMPs相互作用。然而,各自的Pex19p结合位点尚不明确,目前对于这些位点是否包含在mPTS中存在争议。通过使用合成肽扫描和酵母双杂交分析,我们确定并表征了酿酒酵母的两个PMPs即Pex11p和Pex13p中的Pex19p结合位点。结果表明,这些位点由一个最短长度为11个氨基酸的短螺旋基序组成。利用所获得的数据,通过应用模式搜索和预测矩阵,有可能预测并通过实验验证其他几种PMPs中的Pex19p结合位点。在没有Pex19p结合位点的情况下,一个过氧化物酶体靶向的Pex13p片段会错误定位于内质网。通过添加Pex11p的异源结合位点,Pex13p片段的过氧化物酶体靶向得以恢复。我们得出结论,Pex19p结合位点是明确的实体,代表了mPTS的一个重要部分。