Selective N-glycan editing on living cell surfaces to probe glycoconjugate function
文献类型:期刊论文
作者 | Tang, Feng1,2,3; Zhou, Mang1; Qin, Ken1,2; Shi, Wei1,2; Yashinov, Ansor1,2; Yang, Yang1; Yang, Liyun1; Guan, Dongliang1; Zhao, Lei1; Tang, Yubo1 |
刊名 | NATURE CHEMICAL BIOLOGY
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出版日期 | 2020-06-01 |
页码 | 15 |
ISSN号 | 1552-4450 |
DOI | 10.1038/s41589-020-0551-8 |
通讯作者 | Zhou, Mang(mzhou@simm.ac.cn) ; Huang, Wei(huangwei@simm.ac.cn) |
英文摘要 | Cell surfaces are glycosylated in various ways with high heterogeneity, which usually leads to ambiguous conclusions about glycan-involved biological functions. Here, we describe a two-step chemoenzymatic approach for N-glycan-subtype-selective editing on the surface of living cells that consists of a first 'delete' step to remove heterogeneous N-glycoforms of a certain subclass and a second 'insert' step to assemble a well-defined N-glycan back onto the pretreated glyco-sites. Such glyco-edited cells, carrying more homogeneous oligosaccharide structures, could enable precise understanding of carbohydrate-mediated functions. In particular, N-glycan-subtype-selective remodeling and imaging with different monosaccharide motifs at the non-reducing end were successfully achieved. Using a combination of the expression system of the Lec4 CHO cell line and this two-step glycan-editing approach, opioid receptor delta 1 (OPRD1) was investigated to correlate its glycostructures with the biological functions of receptor dimerization, agonist-induced signaling and internalization. |
WOS关键词 | CHEMOENZYMATIC SYNTHESIS ; IGG ANTIBODIES ; ACETYLGLUCOSAMINIDASE ; GLYCOSYLATION ; GLYCOPROTEINS ; MUTANTS ; IDENTIFICATION ; GLYCOPEPTIDES ; STRATEGY ; TRANSGLYCOSYLATION |
资助项目 | National Natural Science Foundation of China[21877116] ; National Science & Technology Major Project 'Key New Drug Creation and Manufacturing Program' of China[2018ZX09711002-006] ; China Postdoctoral Science Foundation[BX20180339] ; China Postdoctoral Science Foundation[2018M642120] |
WOS研究方向 | Biochemistry & Molecular Biology |
语种 | 英语 |
WOS记录号 | WOS:000537039100005 |
出版者 | NATURE PUBLISHING GROUP |
源URL | [http://119.78.100.183/handle/2S10ELR8/280004] ![]() |
专题 | 中国科学院上海药物研究所 |
通讯作者 | Zhou, Mang; Huang, Wei |
作者单位 | 1.Chinese Acad Sci, Ctr Biotherapeut Discovery Res, Shanghai Inst Mat Med, CAS Key Lab Receptor Res,CAS Ctr Excellence Mol C, Shanghai, Peoples R China 2.Univ Chinese Acad Sci, Beijing, Peoples R China 3.Univ Chinese Acad Sci, Sch Pharmaceut Sci & Technol, Hangzhou Inst Adv Study, Hangzhou, Peoples R China 4.East China Normal Univ, Inst Biomed Sci, Shanghai Key Lab Regulatory Biol, Shanghai, Peoples R China 5.East China Normal Univ, Sch Life Sci, Shanghai, Peoples R China |
推荐引用方式 GB/T 7714 | Tang, Feng,Zhou, Mang,Qin, Ken,et al. Selective N-glycan editing on living cell surfaces to probe glycoconjugate function[J]. NATURE CHEMICAL BIOLOGY,2020:15. |
APA | Tang, Feng.,Zhou, Mang.,Qin, Ken.,Shi, Wei.,Yashinov, Ansor.,...&Huang, Wei.(2020).Selective N-glycan editing on living cell surfaces to probe glycoconjugate function.NATURE CHEMICAL BIOLOGY,15. |
MLA | Tang, Feng,et al."Selective N-glycan editing on living cell surfaces to probe glycoconjugate function".NATURE CHEMICAL BIOLOGY (2020):15. |
入库方式: OAI收割
来源:上海药物研究所
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