Brocard Cécile, Hartig Andreas
Max F Perutz Laboratories, University of Vienna, Department of Biochemistry, Dr. Bohrgasse 9, 1030 Vienna, Austria.
Biochim Biophys Acta. 2006 Dec;1763(12):1565-73. doi: 10.1016/j.bbamcr.2006.08.022. Epub 2006 Aug 24.
Originally, the peroxisomal targeting signal 1 (PTS1) was defined as a tripeptide at the C-terminus of proteins prone to be imported into the peroxisomal matrix. The corresponding receptor PEX5 initiates the translocation of proteins by identifying potential substrates via their C-termini and trapping PTS1s through remodeling of its TPR domain. Thorough studies on the interaction between PEX5 and PTS1 as well as sequence-analytic tools revealed the influence of amino acid residues further upstream of the ultimate tripeptide. Altogether, PTS1s should be defined as dodecamer sequences at the C-terminal ends of proteins. These sequences accommodate physical contacts with both the surface and the binding cavity of PEX5 and ensure accessibility of the extreme C-terminus. Knowledge-based approaches in applied Bioinformatics provide reliable tools to accurately predict the peroxisomal location of proteins not yet determined experimentally.
最初,过氧化物酶体靶向信号1(PTS1)被定义为蛋白质C末端的一个三肽,这类蛋白质易于被导入过氧化物酶体基质。相应的受体PEX5通过识别蛋白质的C末端潜在底物并通过其TPR结构域的重塑捕获PTS1来启动蛋白质的转运。对PEX5与PTS1之间相互作用以及序列分析工具的深入研究揭示了最终三肽上游更远的氨基酸残基的影响。总之,PTS1应被定义为蛋白质C末端的十二聚体序列。这些序列可与PEX5的表面和结合腔进行物理接触,并确保极端C末端的可及性。应用生物信息学中基于知识的方法提供了可靠的工具,可准确预测尚未通过实验确定的蛋白质的过氧化物酶体定位。