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J Biol Chem. 2016 Oct 28;291(44):23305-23317. Epub 2016 Sep 14.

Generation of a Mutant Mucor hiemalis Endoglycosidase That Acts on Core-fucosylated N-Glycans.

Author information

1
From the Graduate School of Biostudies, Kyoto University, Kyoto 606-8502, Japan, tkatoh@lif.kyoto-u.ac.jp.
2
From the Graduate School of Biostudies, Kyoto University, Kyoto 606-8502, Japan.
3
the Host-Microbe Interaction Research Laboratory and.
4
the Research Institute for Bioresources and Biotechnology, Ishikawa Prefectural University, Nonoichi, Ishikawa 921-8836, Japan, and.
5
Tokyo Chemical Industry Co., Ltd., 6-15-9 Toshima, Kita-ku, Tokyo 114-0003, Japan.

Abstract

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.

KEYWORDS:

Endo-M; N-linked glycosylation; core fucose; endo-β-N-acetylglucosaminidase; glycoconjugate; glycoprotein; glycosidase; glycoside hydrolase; transglycosylation

PMID:
27629418
PMCID:
PMC5087746
DOI:
10.1074/jbc.M116.737395
[Indexed for MEDLINE]
Free PMC Article

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