Tanaka Yoshimasa, Nishikawa Megumi, Kamisaki Kaho, Hachiya Saki, Nakamura Moeka, Kuwazuru Takahiro, Tanimura Susumu, Soyano Kiyoshi, Takeda Kohsuke
Center for Medical Innovation, Nagasaki University, 1-7-1 Sakamoto, Nagasaki, 852-8588, Japan.
Department of Cell Regulation, Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki, 852-8521, Japan.
Inflamm Regen. 2022 Jun 3;42(1):18. doi: 10.1186/s41232-022-00207-9.
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) and five constant domains (C); of these, V can recognize a variety of foreign antigens. A V 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.
作为自身免疫性疾病治疗药物的来源,海洋衍生生物分子受到了越来越多的关注。长崎县岛屿众多,被大海、海峡、海湾、港湾和小海湾环绕,其海岸线长度在日本仅次于北海道,位居第二。我们已经收集了2万多种海洋微生物,并一直在制备一个原始的海洋微生物提取物文库,该文库包含可能穿透细胞膜并干扰细胞内蛋白质 - 蛋白质相互作用的中小分子生物分子,这些相互作用参与了诸如家族性地中海热等自身炎症性疾病的发展。此外,我们一直在开发一种室内鲨鱼养殖系统,以制备鲨鱼纳米抗体,这些纳米抗体可被开发为自身免疫性疾病的潜在治疗药物。鲨鱼产生重链抗体,称为免疫球蛋白新抗原受体(IgNARs),由一个可变结构域(V)和五个恒定结构域(C)组成;其中,V可以识别多种外来抗原。一种称为纳米抗体的V单结构域片段可以在大肠杆菌中表达,并且具有作为自身免疫性疾病理想治疗候选物的特性。鲨鱼纳米抗体包含互补决定区,这些区域通过可变、多样和连接片段的体细胞重排形成,伴随着片段末端修剪以及N和P添加,这与哺乳动物抗体可变结构域中的情况相同。因此,预计鲨鱼纳米抗体的亲和力和多样性与哺乳动物抗体相当。此外,鲨鱼纳米抗体物理性质稳定,制备成本低廉;因此,它们未来可能会促成高特异性、稳定、有效且廉价的生物治疗药物的开发。在这篇综述中,我们首先总结了用于自身免疫性疾病的传统小分子药物和单克隆抗体疗法的发展历程,然后介绍了我们在长崎大学的药物发现系统,包括原始海洋微生物提取物文库的制备以及鲨鱼纳米抗体的开发。