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Marine-derived microbes and molecules for drug discovery

Increasing attention has been paid to marine-derived biomolecules as sources of therapeutics for autoimmune diseases. Nagasaki Prefecture has many islands and is surrounded by seas, straits, gulfs, bays, and coves, giving it the second longest coastline in Japan after Hokkaido. We have collected mor...

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Autores principales: Tanaka, Yoshimasa, Nishikawa, Megumi, Kamisaki, Kaho, Hachiya, Saki, Nakamura, Moeka, Kuwazuru, Takahiro, Tanimura, Susumu, Soyano, Kiyoshi, Takeda, Kohsuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164490/
https://www.ncbi.nlm.nih.gov/pubmed/35655291
http://dx.doi.org/10.1186/s41232-022-00207-9
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author Tanaka, Yoshimasa
Nishikawa, Megumi
Kamisaki, Kaho
Hachiya, Saki
Nakamura, Moeka
Kuwazuru, Takahiro
Tanimura, Susumu
Soyano, Kiyoshi
Takeda, Kohsuke
author_facet Tanaka, Yoshimasa
Nishikawa, Megumi
Kamisaki, Kaho
Hachiya, Saki
Nakamura, Moeka
Kuwazuru, Takahiro
Tanimura, Susumu
Soyano, Kiyoshi
Takeda, Kohsuke
author_sort Tanaka, Yoshimasa
collection PubMed
description Increasing attention has been paid to marine-derived biomolecules as sources of therapeutics for autoimmune diseases. Nagasaki Prefecture has many islands and is surrounded by seas, straits, gulfs, bays, and coves, giving it the second longest coastline in Japan after Hokkaido. We have collected more than 20,000 marine microbes and have been preparing an original marine microbial extract library, which contains small and mid-size biomolecules that may penetrate cell membranes and interfere with the intracellular protein–protein interaction involved in the development of autoinflammatory diseases such as familial Mediterranean fever. In addition, we have been developing an indoor shark farming system to prepare shark nanobodies that could be developed as potential therapeutic agents for autoimmune diseases. Sharks produce heavy-chain antibodies, called immunoglobulin new antigen receptors (IgNARs), consisting of one variable domain (V(NAR)) and five constant domains (C(NAR)); of these, V(NAR) can recognize a variety of foreign antigens. A V(NAR) single domain fragment, called a nanobody, can be expressed in Escherichia coli and has the properties of an ideal therapeutic candidate for autoimmune diseases. Shark nanobodies contain complementarity-determining regions that are formed through the somatic rearrangement of variable, diversity, and joining segments, with the segment end trimming and the N- and P-additions, as found in the variable domains of mammalian antibodies. The affinity and diversity of shark nanobodies are thus expected to be comparable to those of mammalian antibodies. In addition, shark nanobodies are physically robust and can be prepared inexpensively; as such, they may lead to the development of highly specific, stable, effective, and inexpensive biotherapeutics in the future. In this review, we first summarize the history of the development of conventional small molecule drugs and monoclonal antibody therapeutics for autoimmune diseases, and then introduce our drug discovery system at Nagasaki University, including the preparation of an original marine microbial extract library and the development of shark nanobodies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41232-022-00207-9.
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spelling pubmed-91644902022-06-05 Marine-derived microbes and molecules for drug discovery Tanaka, Yoshimasa Nishikawa, Megumi Kamisaki, Kaho Hachiya, Saki Nakamura, Moeka Kuwazuru, Takahiro Tanimura, Susumu Soyano, Kiyoshi Takeda, Kohsuke Inflamm Regen Review Increasing attention has been paid to marine-derived biomolecules as sources of therapeutics for autoimmune diseases. Nagasaki Prefecture has many islands and is surrounded by seas, straits, gulfs, bays, and coves, giving it the second longest coastline in Japan after Hokkaido. We have collected more than 20,000 marine microbes and have been preparing an original marine microbial extract library, which contains small and mid-size biomolecules that may penetrate cell membranes and interfere with the intracellular protein–protein interaction involved in the development of autoinflammatory diseases such as familial Mediterranean fever. In addition, we have been developing an indoor shark farming system to prepare shark nanobodies that could be developed as potential therapeutic agents for autoimmune diseases. Sharks produce heavy-chain antibodies, called immunoglobulin new antigen receptors (IgNARs), consisting of one variable domain (V(NAR)) and five constant domains (C(NAR)); of these, V(NAR) can recognize a variety of foreign antigens. A V(NAR) single domain fragment, called a nanobody, can be expressed in Escherichia coli and has the properties of an ideal therapeutic candidate for autoimmune diseases. Shark nanobodies contain complementarity-determining regions that are formed through the somatic rearrangement of variable, diversity, and joining segments, with the segment end trimming and the N- and P-additions, as found in the variable domains of mammalian antibodies. The affinity and diversity of shark nanobodies are thus expected to be comparable to those of mammalian antibodies. In addition, shark nanobodies are physically robust and can be prepared inexpensively; as such, they may lead to the development of highly specific, stable, effective, and inexpensive biotherapeutics in the future. In this review, we first summarize the history of the development of conventional small molecule drugs and monoclonal antibody therapeutics for autoimmune diseases, and then introduce our drug discovery system at Nagasaki University, including the preparation of an original marine microbial extract library and the development of shark nanobodies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41232-022-00207-9. BioMed Central 2022-06-03 /pmc/articles/PMC9164490/ /pubmed/35655291 http://dx.doi.org/10.1186/s41232-022-00207-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Tanaka, Yoshimasa
Nishikawa, Megumi
Kamisaki, Kaho
Hachiya, Saki
Nakamura, Moeka
Kuwazuru, Takahiro
Tanimura, Susumu
Soyano, Kiyoshi
Takeda, Kohsuke
Marine-derived microbes and molecules for drug discovery
title Marine-derived microbes and molecules for drug discovery
title_full Marine-derived microbes and molecules for drug discovery
title_fullStr Marine-derived microbes and molecules for drug discovery
title_full_unstemmed Marine-derived microbes and molecules for drug discovery
title_short Marine-derived microbes and molecules for drug discovery
title_sort marine-derived microbes and molecules for drug discovery
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164490/
https://www.ncbi.nlm.nih.gov/pubmed/35655291
http://dx.doi.org/10.1186/s41232-022-00207-9
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