CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences (CAS), Shanghai, China.
Subcell Biochem. 2024;104:425-458. doi: 10.1007/978-3-031-58843-3_16.
Glycosylphosphatidylinositol (GPI) anchoring of proteins is a ubiquitous posttranslational modification in eukaryotic cells. GPI-anchored proteins (GPI-APs) play critical roles in enzymatic, signaling, regulatory, and adhesion processes. Over 20 enzymes are involved in GPI synthesis, attachment to client proteins, and remodeling after attachment. The GPI transamidase (GPI-T), a large complex located in the endoplasmic reticulum membrane, catalyzes the attachment step by replacing a C-terminal signal peptide of proproteins with GPI. In the last three decades, extensive research has been conducted on the mechanism of the transamidation reaction, the components of the GPI-T complex, the role of each subunit, and the substrate specificity. Two recent studies have reported the three-dimensional architecture of GPI-T, which represent the first structures of the pathway. The structures provide detailed mechanisms for assembly that rationalizes previous biochemical results and subunit-dependent stability data. While the structural data confirm the catalytic role of PIGK, which likely uses a caspase-like mechanism to cleave the proproteins, they suggest that unlike previously proposed, GPAA1 is not a catalytic subunit. The structures also reveal a shared cavity for GPI binding. Somewhat unexpectedly, PIGT, a single-pass membrane protein, plays a crucial role in GPI recognition. Consistent with the assembly mechanisms and the active site architecture, most of the disease mutations occur near the active site or the subunit interfaces. Finally, the catalytic dyad is located ~22 Å away from the membrane interface of the GPI-binding site, and this architecture may confer substrate specificity through topological matching between the substrates and the elongated active site. The research conducted thus far sheds light on the intricate processes involved in GPI anchoring and paves the way for further mechanistic studies of GPI-T.
糖基磷脂酰肌醇(GPI)锚定蛋白是真核细胞中普遍存在的一种翻译后修饰。GPI 锚定蛋白(GPI-APs)在酶学、信号转导、调节和黏附过程中发挥着关键作用。超过 20 种酶参与 GPI 的合成、与靶蛋白的连接以及连接后的重塑。GPI 转酰胺酶(GPI-T)是一种位于内质网膜上的大型复合物,通过用 GPI 替换前蛋白的 C 末端信号肽来催化连接步骤。在过去的三十年中,人们对转酰胺反应的机制、GPI-T 复合物的组成、每个亚基的作用以及底物特异性进行了广泛的研究。最近的两项研究报告了 GPI-T 的三维结构,这是该途径的第一个结构。这些结构为组装提供了详细的机制,使以前的生化结果和亚基依赖性稳定性数据合理化。虽然结构数据证实了 PIGK 的催化作用,它可能使用类似半胱天冬酶的机制来切割前蛋白,但它们表明与之前提出的不同,GPAA1 不是一个催化亚基。这些结构还揭示了一个用于 GPI 结合的共享腔。有些出乎意料的是,单次跨膜蛋白 PIGT 在 GPI 识别中发挥着关键作用。与组装机制和活性位点结构一致,大多数疾病突变发生在活性位点或亚基界面附近。最后,催化二联体距离 GPI 结合位点的膜界面约 22 Å,这种结构可能通过将底物与伸长的活性位点进行拓扑匹配来赋予底物特异性。迄今为止的研究揭示了 GPI 锚定所涉及的复杂过程,并为进一步研究 GPI-T 的机制奠定了基础。