Direct conversion of a general antibody to its catalytic antibody and corresponding applications -Importance and role of Pro95 in CDR-3.


Journal

Proceedings of the Japan Academy. Series B, Physical and biological sciences
ISSN: 1349-2896
Titre abrégé: Proc Jpn Acad Ser B Phys Biol Sci
Pays: Japan
ID NLM: 9318162

Informations de publication

Date de publication:
2023
Historique:
medline: 20 6 2023
pubmed: 19 6 2023
entrez: 18 6 2023
Statut: ppublish

Résumé

Catalytic antibodies possess unique features capable of both recognizing and enzymatically degrading antigens. Therefore, they are more beneficial than monoclonal antibodies (mAbs). Catalytic antibodies exhibit the ability to degrade peptides, antigenic proteins, DNA, and physiologically active molecules. However, they have a significant drawback in terms of their production. The production of a desired catalytic antibody has extensive costs, in terms of time and effort. We herein describe an evolutionary method to produce a desired catalytic antibody via conversion of a general antibody by the deletion of Pro95, which resides in complementarity-determining region-3. As over thousands of mAbs have been produced since 1975, using the novel technology discussed herein, the catalytic feature cleaving the antigen can be conferred to the mAb. In this review article, we discussed in detail not only the role of Pro95 but also the unique features of the converted catalytic antibodies. This technique will accelerate research on therapeutic application of catalytic antibodies.

Identifiants

pubmed: 37331814
doi: 10.2183/pjab.99.010
pmc: PMC10319470
doi:

Substances chimiques

Antibodies, Catalytic 0
Antibodies, Monoclonal 0

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

155-172

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Auteurs

Emi Hifumi (E)

Institute for Research Management, Oita University.
Research Center for GLOBAL/LOCAL Infectious Diseases, Oita University.

Hiroaki Taguchi (H)

Faculty of Pharmaceutical Sciences, Suzuka University of Medical Science.

Tamami Nonaka (T)

Research Center for GLOBAL/LOCAL Infectious Diseases, Oita University.

Taizo Uda (T)

Institute for Research Management, Oita University.
Nanotechnology Laboratory, Institute of Systems, Information Technologies and Nanotechnologies (ISIT).

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Classifications MeSH