Neutralizing chimeric heavy-chain antibody targeting the L-HN domain of Clostridium botulinum neurotoxin type F.

BoNT/F Heavy-chain antibody L-HN domain Phage display library

Journal

Archives of toxicology
ISSN: 1432-0738
Titre abrégé: Arch Toxicol
Pays: Germany
ID NLM: 0417615

Informations de publication

Date de publication:
23 Sep 2024
Historique:
received: 07 07 2024
accepted: 10 09 2024
medline: 23 9 2024
pubmed: 23 9 2024
entrez: 23 9 2024
Statut: aheadofprint

Résumé

Botulinum toxin (BoNT) from Clostridium botulinum is the most toxic biotoxin known and is also an important bioterrorism agent. After poisoning, the only effective treatment is injection of antitoxin. However, neutralizing nanoantibodies are safer and more effective, representing a promising therapeutic approach. Therefore, it is important to obtain effective neutralizing nanoantibodies. Hence, the present study aimed to construct a phage antibody library by immunizing a camel and screening specific clones that bind to the L-HN domain of BoNT/F and constructing chimeric heavy-chain antibodies by fusing them with a human Fc fragment. The antibodies' affinity and in vivo neutralizing activities were evaluated. The results showed that 2 µg of F20 antibody could completely neutralize 20 × the median lethal dose (LD

Identifiants

pubmed: 39311906
doi: 10.1007/s00204-024-03869-1
pii: 10.1007/s00204-024-03869-1
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Kaiyue Sun (K)

Institute of Materia Medica, School of Pharmacy, North Sichuan Medical College, Nanchong, China.
Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Shudi Luo (S)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Yujia Jiang (Y)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Jiazheng Guo (J)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Xi Wang (X)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Kexuan Cheng (K)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Changyan Xu (C)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Yixiao Zhang (Y)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Chen Gao (C)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Jiansheng Lu (J)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Peng Du (P)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Yunzhou Yu (Y)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.

Rong Wang (R)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China. wangrong_8312@163.com.

Zhixin Yang (Z)

Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China. yy_xiao@126.com.

Chunyang Zhou (C)

Institute of Materia Medica, School of Pharmacy, North Sichuan Medical College, Nanchong, China. zhouchunyang@nsmc.edu.cn.

Classifications MeSH