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Screening and characterization of inhibitory vNAR targeting nanodisc-assembled influenza M2 proteins
Yu, Chuandi1,2; Ding, Wen3; Zhu, Lei; Zhou, Yuhang1,4; Dong, Yingkui1,5; Li, Ling1; Liu, Juanjuan; Wang, Yizhuo2; Li, Zehua2; Zhu, Lina2; Chen, FaJun; Ruan, Maosen; Qian, Dongming6; Wang, Yujuan; Wu, Bo; Xu, Huangtao; Li, Ming1,2; Bi, Yunchen7,8; Wang, Hao7,8; Wang, Weiqian9; Chao, Peng9; Xing, Lei1; Shen, Bing3; Dai, Han; Zha, Lisha4; Zhao, Hongxin1,6; Wang, Junfeng1,2,5
2023-01-20
发表期刊ISCIENCE
卷号26期号:1页码:21
通讯作者Zha, Lisha(zhalisha@ahau.edu.cn) ; Zhao, Hongxin(zhx@hmfl.ac.cn) ; Wang, Junfeng(junfeng@hmfl.ac.cn)
摘要Influenza A virus poses a constant challenge to human health. The highly conserved influenza matrix-2 (M2) protein is an attractive target for the development of a universal antibody-based drug. However, screening using antigens with subphysiological conformation in a nonmembrane environment significantly reduces the generation of efficient antibodies. Here, M2(1-46) was incorporated into nanodiscs (M2-nanodiscs) with M2 in a membrane-embedded tetrameric conformation, closely resembling its natural physiological state in the influenza viral envelope. M2-nanodisc generation, an antigen, was followed by Chiloscyllium plagiosum immunization. The functional vNARs were selected by phage display panning strategy from the shark immune library. One of the isolated vNARs, AM2H10, could specifically bind to tetrameric M2 instead of monomeric M2e (the ectodomain of M2 protein). Furthermore, AM2H10 blocked ion influx through amantadine-sensitive and resistant M2 channels. Our findings indicated the possibility of developing functional shark nanobodies against various influenza viruses by targeting the M2 protein.
DOI10.1016/j.isci.2022.105736
收录类别SCI
语种英语
资助项目Anhui Technologies Major Program[201903a07020026] ; Chinese Academy of Sciences[YZJJZX202004] ; Users with Excellence Program of Hefei Science Center,CAS[2020HSC-UE018] ; National Natural Science Foundation of China[41876168] ; Taishan Young Scholar Program of Shandong Province[tsqn201812108]
WOS研究方向Science & Technology - Other Topics
WOS类目Multidisciplinary Sciences
WOS记录号WOS:000901534700006
出版者CELL PRESS
WOS关键词INTEGRAL MEMBRANE-PROTEINS ; SINGLE-DOMAIN ; MONOCLONAL-ANTIBODY ; LIPID-BILAYERS ; A VIRUSES ; V-REGION ; SHARK ; CHANNEL ; GENERATION ; SELECTION
引用统计
被引频次:4[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/183261
专题实验海洋生物学重点实验室
通讯作者Zha, Lisha; Zhao, Hongxin; Wang, Junfeng
作者单位1.Chinese Acad Sci, Hefei Inst Phys Sci, High Magnet Field Lab, Key Lab High Magnet Field & Ion Beam Phys Biol, Hefei 230031, Anhui, Peoples R China
2.Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China
3.Anhui Med Univ, Sch Basic Med Sci, Hefei 230032, Anhui, Peoples R China
4.Anhui Agr Univ, Int Immunol Ctr, Hefei 230036, Anhui, Peoples R China
5.Anhui Univ, Inst Phys Sci & Informat Technol, Hefei 230039, Anhui, Peoples R China
6.Hefei China Sci Longwood Biol Technol Co Ltd, Hefei 230088, Anhui, Peoples R China
7.Chinese Acad Sci, Inst Oceanol, Ctr OceanMega Sci, CAS & Shandong Prov Key Lab Expt Marine Biol, Qingdao 266071, Shandong, Peoples R China
8.Pilot Natl Lab Marine Sci & Technol Qingdao, Marine Biol & Biotechnol Lab, Qingdao 266237, Shandong, Peoples R China
9.Chinese Acad Sci, Shanghai Adv Res Inst, Natl Facil Prot Sci Shanghai, Shanghai 201210, Peoples R China
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GB/T 7714
Yu, Chuandi,Ding, Wen,Zhu, Lei,et al. Screening and characterization of inhibitory vNAR targeting nanodisc-assembled influenza M2 proteins[J]. ISCIENCE,2023,26(1):21.
APA Yu, Chuandi.,Ding, Wen.,Zhu, Lei.,Zhou, Yuhang.,Dong, Yingkui.,...&Wang, Junfeng.(2023).Screening and characterization of inhibitory vNAR targeting nanodisc-assembled influenza M2 proteins.ISCIENCE,26(1),21.
MLA Yu, Chuandi,et al."Screening and characterization of inhibitory vNAR targeting nanodisc-assembled influenza M2 proteins".ISCIENCE 26.1(2023):21.
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