Department of Pediatrics, WA Bernbaum Center for Cystic Fibrosis Research, Case Western Reserve University, Cleveland, Ohio 44106, USA.
J Biol Chem. 2013 Jul 5;288(27):19900-14. doi: 10.1074/jbc.M113.477877. Epub 2013 May 20.
Mucin type O-glycosylation is initiated by a large family of polypeptide GalNAc transferases (ppGalNAc Ts) that add α-GalNAc to the Ser and Thr residues of peptides. Of the 20 human isoforms, all but one are composed of two globular domains linked by a short flexible linker: a catalytic domain and a ricin-like lectin carbohydrate binding domain. Presently, the roles of the catalytic and lectin domains in peptide and glycopeptide recognition and specificity remain unclear. To systematically study the role of the lectin domain in ppGalNAc T glycopeptide substrate utilization, we have developed a series of novel random glycopeptide substrates containing a single GalNAc-O-Thr residue placed near either the N or C terminus of the glycopeptide substrate. Our results reveal that the presence and N- or C-terminal placement of the GalNAc-O-Thr can be important determinants of overall catalytic activity and specificity that differ between transferase isoforms. For example, ppGalNAc T1, T2, and T14 prefer C-terminally placed GalNAc-O-Thr, whereas ppGalNAc T3 and T6 prefer N-terminally placed GalNAc-O-Thr. Several transferase isoforms, ppGalNAc T5, T13, and T16, display equally enhanced N- or C-terminal activities relative to the nonglycosylated control peptides. This N- and/or C-terminal selectivity is presumably due to weak glycopeptide binding to the lectin domain, whose orientation relative to the catalytic domain is dynamic and isoform-dependent. Such N- or C-terminal glycopeptide selectivity provides an additional level of control or fidelity for the O-glycosylation of biologically significant sites and suggests that O-glycosylation may in some instances be exquisitely controlled.
粘蛋白型 O-糖基化是由一大类多肽 N-乙酰半乳糖胺转移酶(ppGalNAcTs)启动的,这些酶将 α-GalNAc 添加到肽的丝氨酸和苏氨酸残基上。在 20 个人类同工型中,除了一个之外,其他所有同工型都由两个球形结构域通过一个短的柔性接头连接而成:一个催化结构域和一个蓖麻毒素样凝集素碳水化合物结合结构域。目前,催化结构域和凝集素结构域在肽和糖肽识别和特异性中的作用仍不清楚。为了系统研究凝集素结构域在 ppGalNAcT 糖肽底物利用中的作用,我们开发了一系列含有单个 GalNAc-O-Thr 残基的新型随机糖肽底物,该残基位于糖肽底物的 N 或 C 末端附近。我们的结果表明,GalNAc-O-Thr 的存在和 N 或 C 末端位置可能是决定不同同工型整体催化活性和特异性的重要因素。例如,ppGalNAcT1、T2 和 T14 优先 C 末端的 GalNAc-O-Thr,而 ppGalNAcT3 和 T6 优先 N 末端的 GalNAc-O-Thr。几个转移酶同工型,如 ppGalNAcT5、T13 和 T16,相对于非糖基化对照肽,具有同等增强的 N 或 C 末端活性。这种 N 或 C 末端选择性可能是由于凝集素结构域对糖肽的弱结合,其相对于催化结构域的取向是动态的且依赖于同工型。这种 N 或 C 末端糖肽选择性为生物相关位点的 O-糖基化提供了额外的控制或保真度水平,并表明 O-糖基化在某些情况下可能受到精细控制。