Katoh Toshihiko, Katayama Takane, Tomabechi Yusuke, Nishikawa Yoshihide, Kumada Jyunichi, Matsuzaki Yuji, Yamamoto Kenji
From the Graduate School of Biostudies, Kyoto University, Kyoto 606-8502, Japan,
From the Graduate School of Biostudies, Kyoto University, Kyoto 606-8502, Japan.
J Biol Chem. 2016 Oct 28;291(44):23305-23317. doi: 10.1074/jbc.M116.737395. Epub 2016 Sep 14.
Endo-β-N-acetylglucosaminidase M (Endo-M), an endoglycosidase from the fungus Mucor hiemalis, is a useful tool for chemoenzymatic synthesis of glycoconjugates, including glycoprotein-based therapeutics having a precisely defined glycoform, by virtue of its transglycosylation activity. Although Endo-M has been known to act on various N-glycans, it does not act on core-fucosylated N-glycans, which exist widely in mammalian glycoproteins, thus limiting its application. Therefore, we performed site-directed mutagenesis on Endo-M to isolate mutant enzymes that are able to act on mammalian-type core-α1,6-fucosylated glycans. Among the Endo-M mutant enzymes generated, those in which the tryptophan at position 251 was substituted with alanine or asparagine showed altered substrate specificities. Such mutant enzymes exhibited increased hydrolysis of a synthetic α1,6-fucosylated trimannosyl core structure, whereas their activity on the afucosylated form decreased. In addition, among the Trp-251 mutants, the W251N mutant was most efficient in hydrolyzing the core-fucosylated substrate. W251N mutants could act on the immunoglobulin G-derived core-fucosylated glycopeptides and human lactoferrin glycoproteins. This mutant was also capable of transferring the sialyl glycan from an activated substrate intermediate (sialyl glyco-oxazoline) onto an α1,6-fucosyl-N-acetylglucosaminyl biotin. Furthermore, the W251N mutant gained a glycosynthase-like activity when a N175Q substitution was introduced and it caused accumulation of the transglycosylation products. These findings not only give insights into the substrate recognition mechanism of glycoside hydrolase family 85 enzymes but also widen their scope of application in preparing homogeneous glycoforms of core-fucosylated glycoproteins for the production of potent glycoprotein-based therapeutics.
内切-β-N-乙酰氨基葡萄糖苷酶M(Endo-M)是一种来自冬黑麂酶菌的内切糖苷酶,由于其转糖基化活性,它是化学酶法合成糖缀合物(包括具有精确确定糖型的基于糖蛋白的治疗药物)的有用工具。尽管已知Endo-M作用于各种N-聚糖,但它不作用于广泛存在于哺乳动物糖蛋白中的核心岩藻糖基化N-聚糖,因此限制了其应用。因此,我们对Endo-M进行了定点诱变,以分离能够作用于哺乳动物型核心α1,6-岩藻糖基化聚糖的突变酶。在产生的Endo-M突变酶中,第251位色氨酸被丙氨酸或天冬酰胺取代的那些酶表现出改变的底物特异性。这种突变酶对合成的α1,6-岩藻糖基化三甘露糖基核心结构的水解增加,而它们对去岩藻糖基化形式的活性降低。此外,在Trp-251突变体中,W251N突变体在水解核心岩藻糖基化底物方面最有效。W251N突变体可以作用于免疫球蛋白G衍生的核心岩藻糖基化糖肽和人乳铁蛋白糖蛋白。该突变体还能够将唾液酸聚糖从活化的底物中间体(唾液酸糖恶唑啉)转移到α1,6-岩藻糖基-N-乙酰氨基葡萄糖基生物素上。此外,当引入N175Q取代时,W251N突变体获得了类似糖合酶的活性,并导致转糖基化产物的积累。这些发现不仅深入了解了糖苷水解酶家族85酶的底物识别机制,还拓宽了它们在制备用于生产强效基于糖蛋白的治疗药物的核心岩藻糖基化糖蛋白的均匀糖型方面的应用范围。