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Kinetics of lipid raft formation at lipid monolayer-bilayer junction probed by surface plasmon resonance

机译:表面等离子体共振探测脂质单层 - 双层结的脂筏形成动力学

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摘要

A label-free, non-dispruptive, and real-time analytical device to monitor the dynamic features of biomolecules and their interactions with neighboring molecules is an essential prerequisite for biochip- and diagonostic assays. To explore one of the central questions on the lipid-lipid interactions in the course of the liquid-ordered (l(o)) domain formation, called rafts, we developed a method of reconstituting continuous but spatially heterogeneous lipid membrane platforms with molayer-bilayer juntions (MBJs) that enable to form the l(o) domains in a spatiotemporally controlled manner. This allows us to detect the time-lapse dynamics of the lipid-lipid interactions during raft formation and resultant membrane phase changes together with the raft-associated receptor-ligand binding through the surface plasmon resonance (SPR). For cross-validation, using epifluorescence microscopy, we demonstrated the underlying mechanisms for raft formations that the infiltration of cholesterols into the sphingolipid-enriched domains plays a crucial roles in the membrane phase-separation. Our membrane platform, being capable of monitoring dynamic interactions among lipids and performing the systematic optical analysis, will unveil physiological roles of cholesterols in a variety of biological events.
机译:无标签,非歧视和实时分析装置,用于监测生物分子的动态特征及其与相邻分子的相互作用是生物芯片和对角测定的必要先决条件。为了探讨液体有序的脂质相互作用的脂质相互作用中的一个中枢性问题,称为筏子,叫做筏,我们开发了一种用熔岩双层重构连续但空间异质的脂质膜平台的方法吊状(MBJ)能够以时空控制的方式形成L(O)域。这使我们能够检测筏子形成期间脂质 - 脂质相互作用的时间流逝动态,并将结果膜相变为通过表面等离子体共振(SPR)的筏相关的受体 - 配体结合。对于交叉验证,使用渗流荧光显微镜检查,我们证明了筏地层的潜在机制,即胆固醇浸入鞘脂素的域中的渗透性在膜相分离中起着至关重要的作用。我们的膜平台能够监测脂质之间的动态相互作用并进行系统光学分析,将在各种生物事件中揭开胆固醇的生理作用。

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