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Differential effects of lipids and lyso-lipids on the mechanosensitivity of the mechanosensitive channels MscL and MscS

机译:脂质和溶血脂对机械敏感性通道MscL和MscS的机械敏感性的差异作用

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摘要

Mechanosensitive (MS) channels of small (MscS) and large (MscL) conductance are the major players in the protection of bacterial cells against hypoosmotic shock. Although a great deal is known about structure and function of these channels, much less is known about how membrane lipids may influence their mechanosensitivity and function. In this study, we use liposome coreconstitution to examine the effects of different types of lipids on MscS and MscL mechanosensitivity simultaneously using the patch-clamp technique and confocal microscopy. Fluorescence lifetime imaging (FLIM)-FRET microscopy demonstrated that coreconstitution of MscS and MscL led to clustering of these channels causing a significant increase in the MscS activation threshold. Furthermore, the MscL/MscS threshold ratio dramatically decreased in thinner compared with thicker bilayers and upon addition of cholesterol, known to affect the bilayer thickness, stiffness and pressure profile. In contrast, application of micromolar concentrations of lysophosphatidylcholine (LPC) led to an increase of the MscL/MscS threshold ratio. These data suggest that differences in hydrophobic mismatch and bilayer stiffness, change in transbilayer pressure profile, and close proximity of MscL and MscS affect the structural dynamics of both channels to a different extent. Our findings may have far-reaching implications for other types of ion channels and membrane proteins that, like MscL and MscS, may coexist in multiple molecular complexes and, consequently, have their activation characteristics significantly affected by changes in the lipid environment and their proximity to each other.
机译:小电导(MscS)和大电导(MscL)的机械敏感(MS)通道是保护细菌细胞抵抗低渗性休克的主要因素。尽管对这些通道的结构和功能的了解很多,但对膜脂质如何影响其机械敏感性和功能的了解却很少。在这项研究中,我们使用脂质体核心构建技术使用膜片钳技术和共聚焦显微镜同时检查了不同类型的脂质对MscS和MscL机械敏感性的影响。荧光寿命成像(FLIM)-FRET显微镜表明,MscS和MscL的核心结构导致这些通道的聚集,从而导致MscS激活阈值显着增加。此外,与较厚的双层相比,较薄的MscL / MscS阈值比率显着降低,并且在添加胆固醇后,胆固醇会降低双层厚度,刚度和压力分布。相反,应用微摩尔浓度的溶血磷脂酰胆碱(LPC)导致MscL / MscS阈值比增加。这些数据表明疏水性不匹配和双层刚度,跨双层压力分布的变化以及MscL和MscS的紧密接近程度的差异在不同程度上影响了两个通道的结构动力学。我们的发现可能对其他类型的离子通道和膜蛋白(如MscL和MscS)可能共存于多种分子复合物中具有深远的影响,因此,它们的活化特性会受到脂质环境的变化及其与脂质的接近程度的影响。彼此。

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