Marine-derived microbes and molecules for drug discovery

被引:3
|
作者
Tanaka, Yoshimasa [1 ]
Nishikawa, Megumi [2 ]
Kamisaki, Kaho [2 ]
Hachiya, Saki [2 ]
Nakamura, Moeka [2 ]
Kuwazuru, Takahiro [3 ]
Tanimura, Susumu [2 ]
Soyano, Kiyoshi [3 ]
Takeda, Kohsuke [2 ]
机构
[1] Nagasaki Univ, Ctr Med Innovat, 1-7-1 Sakamoto, Nagasaki 8528588, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Dept Cell Regulat, 14 Bunkyo Machi, Nagasaki, Japan
[3] Nagasaki Univ, Inst East China Sea Res, Nagasaki 8528131, Japan
关键词
Autoimmune disease; Autoinflammatory disease; Biologic; Conventional drug; Marine microbe; Monoclonal antibody; Nanobody; Rheumatoid arthritis; Shark new antigen receptor; PROSTAGLANDIN SYNTHASE; ANTIGEN RECEPTOR; RHEUMATOID-ARTHRITIS; MESSENGER-RNA; ANTIBODIES; NANOBODIES; DISEASE; INNATE; TNF; CYCLOOXYGENASE;
D O I
10.1186/s41232-022-00207-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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页数:12
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