Organic Chemistry Section, Department of Inorganic and Organic Chemistry, Facultat de Química, Universitat de Barcelona, Diagonal 645, 08028 Barcelona, Catalonia, Spain.
Institut de Biomedicina de la Universitat de Barcelona (IBUB), 08028 Barcelona, Catalonia, Spain.
Molecules. 2023 Jul 6;28(13):5249. doi: 10.3390/molecules28135249.
Amphidinolides are a family of more than forty macrolides of varying sizes and complex structures isolated from dinoflagellates of the genus . Although all of them display potent-to-moderate cytotoxicity, their full bioactivity profile and mode of action have not been fully investigated. Access to enough material is needed for these studies, but samples of these compounds are limited due to the minute amounts that can only be obtained by either large-scale cultivation of the organism that produces them or by total synthesis. Of all the amphidinolides known to date, only the targets of five of them (B1, H1, J, K, and X) have been examined and all have been found to interact with actin, a crucial cytoskeletal protein. This paper reviews what is currently known about actin-interacting amphidinolides, with a focus on the research of our group. Amphidinolides J and X are F-actin destabilizers, whereas Amphidinolides H1 and K stabilize actin filaments, likely via different mechanisms. More precise details of the interaction between amphidinolides and actin are missing.
短沟藻素是一组由四十多种大小和复杂结构不同的大环内酯类化合物组成的家族,从沟鞭藻属的藻类中分离得到。尽管它们都显示出较强到中等的细胞毒性,但它们的完整生物活性谱和作用模式尚未得到充分研究。这些研究需要获得足够的物质,但由于只能通过大规模培养产生这些化合物的生物体或全合成才能获得少量的样品,因此这些化合物的样本有限。迄今为止,在已知的所有短沟藻素中,只有其中五种(B1、H1、J、K 和 X)的靶点得到了研究,所有这些靶点都被发现与肌动蛋白相互作用,肌动蛋白是一种关键的细胞骨架蛋白。本文综述了目前已知的与肌动蛋白相互作用的短沟藻素,重点介绍了我们小组的研究。短沟藻素 J 和 X 是 F-肌动蛋白解聚剂,而短沟藻素 H1 和 K 稳定肌动蛋白丝,可能通过不同的机制。短沟藻素和肌动蛋白之间相互作用的更精确细节尚不清楚。