Islam Md Sirajul, Gaston James P, Baker Matthew A B
School of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, NSW 2052, Australia.
CSIRO Synthetic Biology Future Science Platform, GPO Box 2583, Brisbane, QLD 4001, Australia.
Membranes (Basel). 2021 Nov 4;11(11):857. doi: 10.3390/membranes11110857.
Ion channels are membrane proteins that play important roles in a wide range of fundamental cellular processes. Studying membrane proteins at a molecular level becomes challenging in complex cellular environments. Instead, many studies focus on the isolation and reconstitution of the membrane proteins into model lipid membranes. Such simpler, in vitro, systems offer the advantage of control over the membrane and protein composition and the lipid environment. Rhodopsin and rhodopsin-like ion channels are widely studied due to their light-interacting properties and are a natural candidate for investigation with fluorescence methods. Here we review techniques for synthesizing liposomes and for reconstituting membrane proteins into lipid bilayers. We then summarize fluorescence assays which can be used to verify the functionality of reconstituted membrane proteins in synthetic liposomes.
离子通道是膜蛋白,在广泛的基本细胞过程中发挥重要作用。在复杂的细胞环境中,在分子水平上研究膜蛋白具有挑战性。相反,许多研究集中于膜蛋白的分离以及将其重组到模型脂质膜中。这种更简单的体外系统具有能够控制膜、蛋白质组成和脂质环境的优势。视紫红质和视紫红质样离子通道因其与光相互作用的特性而被广泛研究,并且是用荧光方法进行研究的天然候选对象。在这里,我们综述了合成脂质体以及将膜蛋白重组到脂质双层中的技术。然后,我们总结了可用于验证重组到合成脂质体中的膜蛋白功能的荧光测定法。