Department of Physiology and Biophysics, Weill Cornell Medical College, New York, New York, USA.
Biophys J. 2011 Aug 17;101(4):847-55. doi: 10.1016/j.bpj.2011.07.013.
Alcohols are known modulators of lipid bilayer properties. Their biological effects have long been attributed to their bilayer-modifying effects, but alcohols can also alter protein function through direct protein interactions. This raises the question: Do alcohol's biological actions result predominantly from direct protein-alcohol interactions or from general changes in the membrane properties? The efficacy of alcohols of various chain lengths tends to exhibit a so-called cutoff effect (i.e., increasing potency with increased chain length, which that eventually levels off). The cutoff varies depending on the assay, and numerous mechanisms have been proposed such as: limited size of the alcohol-protein interaction site, limited alcohol solubility, and a chain-length-dependent lipid bilayer-alcohol interaction. To address these issues, we determined the bilayer-modifying potency of 27 aliphatic alcohols using a gramicidin-based fluorescence assay. All of the alcohols tested (with chain lengths of 1-16 carbons) alter the bilayer properties, as sensed by a bilayer-spanning channel. The bilayer-modifying potency of the short-chain alcohols scales linearly with their bilayer partitioning; the potency tapers off at higher chain lengths, and eventually changes sign for the longest-chain alcohols, demonstrating an alcohol cutoff effect in a system that has no alcohol-binding pocket.
醇类是众所周知的脂质双层性质调节剂。它们的生物学效应长期以来归因于它们对双层的修饰作用,但醇类也可以通过直接蛋白质相互作用改变蛋白质功能。这就提出了一个问题:醇类的生物学作用主要是由于直接的蛋白质-醇相互作用还是由于膜性质的一般变化?各种链长的醇的功效往往表现出所谓的截止效应(即随着链长的增加而增加效力,最终趋于平稳)。截止值取决于测定方法,并且已经提出了许多机制,例如:醇-蛋白质相互作用位点的有限大小、醇的有限溶解度以及依赖于链长的脂质双层-醇相互作用。为了解决这些问题,我们使用基于短杆菌肽的荧光测定法测定了 27 种脂肪醇的双层修饰效力。所有测试的醇(具有 1-16 个碳原子的链长)都改变了双层性质,这可以通过横跨双层的通道感知到。短链醇的双层修饰效力与其双层分配线性相关;在更高的链长下,效力逐渐减弱,对于最长链的醇,最终发生变化,表明在没有醇结合口袋的系统中存在醇截止效应。