Tanaka Koji, Caaveiro Jose M M, Morante Koldo, Tsumoto Kouhei
Department of Chemistry and Biotechnology, The University of Tokyo, Bunkyo-ku, Tokyo 113-8656, Japan.
Department of Bioengineering, School of Engineering, The University of Tokyo, Bunkyo-ku, Tokyo 113-8656, Japan
Philos Trans R Soc Lond B Biol Sci. 2017 Aug 5;372(1726). doi: 10.1098/rstb.2016.0216.
Pore-forming toxins (PFTs) are proteins endowed with metamorphic properties that enable them to stably fold in water solutions as well as in cellular membranes. PFTs produce lytic pores on the plasma membranes of target cells conducive to lesions, playing key roles in the defensive and offensive molecular systems of living organisms. Actinoporins are a family of potent haemolytic toxins produced by sea anemones vigorously studied as a paradigm of α-helical PFTs, in the context of lipid-protein interactions, and in connection with nanopore technologies. We have recently reported that fragaceatoxin C (FraC), an actinoporin, engages biological membranes with a large adhesive motif allowing the simultaneous attachment of up to four lipid molecules prior to pore formation. Since actinoporins also interact with carbohydrates, we sought to understand the molecular and energetic basis of glycan recognition by FraC. By employing structural and biophysical methodologies, we show that FraC engages glycans with low affinity using its lipid-binding module. Contrary to other PFTs requiring separate domains for glycan and lipid recognition, the small single-domain actinoporins economize resources by achieving dual recognition with a single binding module. This mechanism could enhance the recruitment of actinoporins to the surface of target tissues in their marine environment.This article is part of the themed issue 'Membrane pores: from structure and assembly, to medicine and technology'.
成孔毒素(PFTs)是一类具有变态特性的蛋白质,这使它们能够在水溶液以及细胞膜中稳定折叠。PFTs可在靶细胞的质膜上形成溶解性孔道,进而导致损伤,在生物体的防御和攻击分子系统中发挥关键作用。放线孔蛋白是海葵产生的一类强效溶血毒素,作为α-螺旋PFTs的范例,在脂蛋白相互作用的背景下以及与纳米孔技术相关的研究中受到了广泛关注。我们最近报道,放线孔蛋白脆性毒素C(FraC)通过一个大的黏附基序与生物膜结合,在形成孔道之前可同时结合多达四个脂质分子。由于放线孔蛋白也与碳水化合物相互作用,我们试图了解FraC识别聚糖的分子和能量基础。通过采用结构和生物物理方法,我们发现FraC利用其脂质结合模块以低亲和力结合聚糖。与其他需要单独结构域进行聚糖和脂质识别的PFTs不同,小的单结构域放线孔蛋白通过一个单一结合模块实现双重识别,从而节省了资源。这种机制可能会增强放线孔蛋白在其海洋环境中向靶组织表面的募集。本文是主题为“膜孔:从结构与组装到医学与技术”的特刊的一部分。