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高温下胆固醇对模型膜的影响研究:Laurdan 和 Patman 的观察结果有所不同。

Examining the effects of cholesterol on model membranes at high temperatures: Laurdan and Patman see it differently.

机构信息

Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84602, USA.

Department of Physiology and Developmental Biology, Brigham Young University, Provo, UT 84602, USA.

出版信息

Biochim Biophys Acta Biomembr. 2018 Aug;1860(8):1571-1579. doi: 10.1016/j.bbamem.2018.05.013. Epub 2018 May 25.

Abstract

At high temperature, the presence of cholesterol in phospholipid membranes alters the influence of membrane dipoles, including water molecules, on naphthalene-based fluorescent probes such as Laurdan and Patman (solvatochromism). Although both of these probes report identical changes to their emission spectra as a function of temperature in pure phosphatidylcholine bilayers, they differ in their response to cholesterol. Computer simulations of the spectra based on a simple model of solvatochromism indicated that the presence of cholesterol reduces the probability of bilayer dipole relaxation and also blunts the tendency of heat to enhance that probability. While the overall effect of cholesterol on membrane dipoles was detected identically by the two probes, Laurdan was influenced much more by the additional effect on temperature sensitivity than was Patman. A comparison of the fluorescence data with simulations using a coarse-grained bilayer model (de Meyer et al., 2010) suggested that these probes may be differentially sensitive to two closely related properties distinguishable in the presence of cholesterol. Specifically, Patman fluorescence correlated best with the average phospholipid acyl chain order. On the other hand, Laurdan fluorescence tracked more closely with the area per lipid molecule which, although affected generally by chain order, is also impacted by additional membrane-condensing effects of cholesterol. We postulate that this difference between Laurdan and Patman may be attributed to the bulkier charged headgroup of Patman which may cause the probe to preferentially locate in juxtaposition to the diminutive headgroup of cholesterol as the membrane condenses.

摘要

在高温下,胆固醇在磷脂膜中的存在改变了膜偶极子(包括水分子)对基于萘的荧光探针(如 Laurdan 和 Patman)的影响(溶剂化变色)。虽然这两种探针在纯磷脂双层中随温度变化其发射光谱的变化相同,但它们对胆固醇的反应不同。基于溶剂化变色的简单模型对光谱的计算机模拟表明,胆固醇的存在降低了双层偶极子弛豫的概率,也削弱了热增强这种概率的趋势。虽然两种探针都能以相同的方式检测到胆固醇对膜偶极子的总体影响,但 Laurdan 受额外的温度敏感性影响比 Patman 大得多。将荧光数据与使用粗粒度双层模型(de Meyer 等人,2010)进行的模拟进行比较表明,这些探针可能对两种在胆固醇存在下可区分的密切相关的性质具有不同的敏感性。具体来说,Patman 荧光与平均磷脂酰基链有序性相关性最好。另一方面,Laurdan 荧光更密切地追踪脂质分子的面积,尽管该面积通常受链有序性的影响,但也受到胆固醇的额外膜浓缩效应的影响。我们假设,Laurdan 和 Patman 之间的这种差异可能归因于 Patman 较大的带电头基,这可能导致探针在膜浓缩时优先与胆固醇微小的头基并列定位。

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