Literature DB >> 32022056

Chemical diversity and mode of action of natural products targeting lipids in the eukaryotic cell membrane.

Shinichi Nishimura1, Nobuaki Matsumori.   

Abstract

Covering: up to 2019Nature furnishes bioactive compounds (natural products) with complex chemical structures, yet with simple, sophisticated molecular mechanisms. When natural products exhibit their activities in cells or bodies, they first have to bind or react with a target molecule in/on the cell. The cell membrane is a major target for bioactive compounds. Recently, our understanding of the molecular mechanism of interactions between natural products and membrane lipids progressed with the aid of newly-developed analytical methods. New technology reconnects old compounds with membrane lipids, while new membrane-targeting molecules are being discovered through the screening for antimicrobial potential of natural products. This review article focuses on natural products that bind to eukaryotic membrane lipids, and includes clinically important molecules and key research tools. The chemical diversity of membrane-targeting natural products and the molecular basis of lipid recognition are described. The history of how their mechanism was unveiled, and how these natural products are used in research are also mentioned.

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Year:  2020        PMID: 32022056     DOI: 10.1039/c9np00059c

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  6 in total

1.  Targeting and extending the eukaryotic druggable genome with natural products.

Authors:  Hendrik Luesch; John B MacMillan
Journal:  Nat Prod Rep       Date:  2020-06-24       Impact factor: 13.423

Review 2.  Marine natural products targeting the eukaryotic cell membrane.

Authors:  Shinichi Nishimura
Journal:  J Antibiot (Tokyo)       Date:  2021-09-07       Impact factor: 2.649

3.  Ceramide Aminoethylphosphonate as a New Molecular Target for Pore-Forming Aegerolysin-Based Protein Complexes.

Authors:  Teresa Balbi; Francesco Trenti; Anastasija Panevska; Gregor Bajc; Graziano Guella; Caterina Ciacci; Barbara Canonico; Laura Canesi; Kristina Sepčić
Journal:  Front Mol Biosci       Date:  2022-05-25

4.  Fungicidal amphotericin B sponges are assemblies of staggered asymmetric homodimers encasing large void volumes.

Authors:  Agnieszka Lewandowska; Corinne P Soutar; Alexander I Greenwood; Evgeny Nimerovsky; Ashley M De Lio; Jordan T Holler; Grant S Hisao; Anuj Khandelwal; Jiabao Zhang; Anna M SantaMaria; Charles D Schwieters; Taras V Pogorelov; Martin D Burke; Chad M Rienstra
Journal:  Nat Struct Mol Biol       Date:  2021-12-09       Impact factor: 18.361

5.  Genomic and Targeted Approaches Unveil the Cell Membrane as a Major Target of the Antifungal Cytotoxin Amantelide A.

Authors:  Lobna A Elsadek; James H Matthews; Shinichi Nishimura; Takahiro Nakatani; Airi Ito; Tongjun Gu; Danmeng Luo; Lilibeth A Salvador-Reyes; Valerie J Paul; Hideaki Kakeya; Hendrik Luesch
Journal:  Chembiochem       Date:  2021-03-23       Impact factor: 3.164

6.  Sterol Sponge Mechanism Is Conserved for Glycosylated Polyene Macrolides.

Authors:  Xiaorui Guo; Jiabao Zhang; Xinyi Li; Emily Xiao; Justin D Lange; Chad M Rienstra; Martin D Burke; Douglas A Mitchell
Journal:  ACS Cent Sci       Date:  2021-04-26       Impact factor: 14.553

  6 in total

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