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

机译:检查胆固醇对高温模型膜的影响:劳丹和帕特曼不同地看到它

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摘要

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.
机译:在高温下,磷脂膜的胆固醇存在改变膜偶极子的影响,包括水分子,在萘基荧光探针如劳丹和帕特曼(SolvatoChromism)。虽然这两种探测器报告其发射光谱的变化与纯磷脂酰胆碱双层的温度的函数相同,但它们对其对胆固醇的反应不同。基于SolvatoChromism的简单模型的基于Spectra的计算机模拟表明胆固醇的存在降低了双层偶极弛豫的概率,并且还钝化了热量以增强这种概率。虽然胆固醇对膜偶联的总体效果被两种探针相同地检测到,但Laurdan的影响更多地受到对温度敏感性的额外影响而不是帕特曼。使用粗粒双层模型进行模拟的荧光数据(De Meyer等,2010)表明这些探针可能对胆固醇存在下可区分的两个密切相关的性能差异敏感。具体地,Patman荧光最佳地与平均磷脂酰基链顺序相关。另一方面,Laurdan荧光与每个脂质分子的面积更接近地跟踪,虽然通常通过链序受影响,但也受到胆固醇的额外膜冷凝效应的影响。我们假设劳丹和帕特曼之间的这种差异可能归因于PATMAN的笨蛋指控的头组,这可能导致探针优先定位在诸如膜冷凝器的胆固醇的逐渐沉积中。

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