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.
引用
收藏
页数:12
相关论文
共 50 条
  • [41] Discovery of Anti-MRSA Secondary Metabolites from a Marine-Derived Fungus Aspergillus fumigatus
    Zhang, Rui
    Wang, Haifeng
    Chen, Baosong
    Dai, Huanqin
    Sun, Jingzu
    Han, Junjie
    Liu, Hongwei
    [J]. MARINE DRUGS, 2022, 20 (05)
  • [42] Discovery and characterization of a cytochalasan biosynthetic cluster from the marine-derived fungusAspergillus flavipesCNL-338
    Heard, Stephanie C.
    Wu, Guangwei
    Winter, Jaclyn M.
    [J]. JOURNAL OF ANTIBIOTICS, 2020, 73 (11): : 803 - 807
  • [43] Iron recycling in marine systems: Of microbes and molecules
    Barbeau, Katherine
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2018, 255
  • [44] Waixenicin A, a marine-derived TRPM7 inhibitor: a promising CNS drug lead
    Sun, Hong-Shuo
    Horgen, F. David
    Romo, Daniel
    Hull, Kenneth G.
    Kiledal, Sigrid A.
    Fleig, Andrea
    Feng, Zhong-Ping
    [J]. ACTA PHARMACOLOGICA SINICA, 2020, 41 (12) : 1519 - 1524
  • [45] Current Status of Marine-Derived Compounds as Warheads in Anti-Tumor Drug Candidates
    Newman, David J.
    Cragg, Gordon M.
    [J]. MARINE DRUGS, 2017, 15 (04):
  • [46] Waixenicin A, a marine-derived TRPM7 inhibitor: a promising CNS drug lead
    Hong-Shuo Sun
    F. David Horgen
    Daniel Romo
    Kenneth G. Hull
    Sigrid A. Kiledal
    Andrea Fleig
    Zhong-Ping Feng
    [J]. Acta Pharmacologica Sinica, 2020, 41 : 1519 - 1524
  • [47] Biotransformation of bioactive marine natural products by the marine-derived microorganisms
    Yun, K.
    Son, B. W.
    [J]. PLANTA MEDICA, 2015, 81 (11) : 918 - 918
  • [48] Valorization of marine-derived wastes as green sorbents
    Cheong, Kah Yein
    Kong, Sieng Huat
    Foong, Shin Ying
    Yek, Peter Nai Yuh
    Nguyen, Thanh-Binh
    Ma, Nyuk Ling
    Dong, Cheng-Di
    Lam, Su Shiung
    [J]. CURRENT OPINION IN GREEN AND SUSTAINABLE CHEMISTRY, 2024, 47
  • [49] The Catalytic Mechanism of the Marine-Derived Macrocyclase PatGmac
    Bras, Natercia F.
    Ferreira, Pedro
    Calixto, Ana R.
    Jaspars, Marcel
    Houssen, Wael
    Naismith, James H.
    Fernandes, Pedro A.
    Ramos, Maria J.
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2016, 22 (37) : 13089 - 13097
  • [50] Symbiotic Microbes from Marine Invertebrates: Driving a New Era of Natural Product Drug Discovery
    Blockley, Alix
    Elliott, David R.
    Roberts, Adam P.
    Sweet, Michael
    [J]. DIVERSITY-BASEL, 2017, 9 (04):