Luo Lin, Xue Jing, Kwan Ann, Gamsjaeger Roland, Wielens Jerome, von Kleist Lisa, Cubeddu Liza, Guo Zhong, Stow Jennifer L, Parker Michael W, Mackay Joel P, Robinson Phillip J
From the Cell Signalling Unit, Children's Medical Research Institute, University of Sydney, New South Wales 2145, Australia, Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland 4072, Australia, IMB Center for Inflammation and Disease Research, University of Queensland, Brisbane, Queensland 4072, Australia.
From the Cell Signalling Unit, Children's Medical Research Institute, University of Sydney, New South Wales 2145, Australia.
J Biol Chem. 2016 Apr 29;291(18):9411-24. doi: 10.1074/jbc.M115.703108. Epub 2016 Feb 18.
Dynamin is a GTPase that mediates vesicle fission during synaptic vesicle endocytosis. Its long C-terminal proline-rich domain contains 13 PXXP motifs, which orchestrate its interactions with multiple proteins. The SH3 domains of syndapin and endophilin bind the PXXP motifs called Site 2 and 3 (Pro-786-Pro-793) at the N-terminal end of the proline-rich domain, whereas the amphiphysin SH3 binds Site 9 (Pro-833-Pro-836) toward the C-terminal end. In some proteins, SH3/peptide interactions also involve short distance elements, which are 5-15 amino acid extensions flanking the central PXXP motif for high affinity binding. Here we found two previously unrecognized elements in the central and the C-terminal end of the dynamin proline-rich domain that account for a significant increase in syndapin binding affinity compared with a previously reported Site 2 and Site 3 PXXP peptide alone. The first new element (Gly-807-Gly-811) is short distance element on the C-terminal side of Site 2 PXXP, which might contact a groove identified under the RT loop of the SH3 domain. The second element (Arg-838-Pro-844) is located about 50 amino acids downstream of Site 2. These two elements provide additional specificity to the syndapin SH3 domain outside of the well described polyproline-binding groove. Thus, the dynamin/syndapin interaction is mediated via a network of multiple contacts outside the core PXXP motif over a previously unrecognized extended region of the proline-rich domain. To our knowledge this is the first example among known SH3 interactions to involve spatially separated and extended long-range elements that combine to provide a higher affinity interaction.
发动蛋白是一种GTP酶,在突触小泡内吞过程中介导小泡裂变。其长的富含脯氨酸的C末端结构域包含13个PXXP基序,这些基序协调其与多种蛋白质的相互作用。Syndapin和内吞蛋白的SH3结构域与富含脯氨酸结构域N末端的称为位点2和位点3(Pro-786-Pro-793)的PXXP基序结合,而发动蛋白SH3结构域与靠近C末端的位点9(Pro-833-Pro-836)结合。在一些蛋白质中,SH3/肽相互作用还涉及短距离元件,这些元件是位于中央PXXP基序两侧的5-15个氨基酸的延伸序列,用于高亲和力结合。在这里,我们在发动蛋白富含脯氨酸结构域的中央和C末端发现了两个以前未被识别的元件,与之前单独报道的位点2和位点3 PXXP肽相比,这两个元件使syndapin结合亲和力显著增加。第一个新元件(Gly-807-Gly-811)是位点2 PXXP C末端一侧的短距离元件,它可能与SH3结构域RT环下方确定的一个凹槽接触。第二个元件(Arg-838-Pro-844)位于位点2下游约50个氨基酸处。这两个元件为syndapin SH3结构域提供了除了已描述的多聚脯氨酸结合凹槽之外的额外特异性。因此,发动蛋白/syndapin相互作用是通过富含脯氨酸结构域一个以前未被识别的延伸区域内核心PXXP基序之外的多个接触网络介导的。据我们所知,这是已知的SH3相互作用中第一个涉及空间上分离且延伸的远程元件组合以提供更高亲和力相互作用的例子。