Separable contributions of ordered and disordered lipid fatty acyl chain segments to νCH2 bands in model and biological membranes: A Fourier transform infrared spectroscopic study

Zoltán Kóta, Mónika Debreczeny, Balázs Szalontai
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Abstract

In this article, the assignment of the ν(CH) stretching region of lipid molecules is revisited. This region is extensively used to follow lipid phase transitions, and especially the frequency shifts and bandwidth alterations in the νsymCH2 band have been utilized in this respect. Here, we propose and prove that behind these phenomena there are pairs of component bands in the cases of both the νsymCH2 and the νasCH2 bands. The lower-frequency components of the pairs are assigned to the vibrations of CH2 groups on trans segments of the fatty acyl chains, while the higher-frequency components of the pairs are assigned to CH2 groups on gauche segments. To prove these assignments, we have shown that the νCH2 frequencies are characteristic of the conformation of the lipid fatty acyl chain itself, and not the state of the whole lipid matrix. Curve fitting in fact revealed the conformer-specific components. With the use of singular value decomposition analysis we have demonstrated that the relative intensity changes in the components, and not the shifts in the whole bands, cause the observed shifts in the νCH2 bands upon lipid phase transition. The results of this approach are presented for deuterium-saturated dioleoyl–phosphatidylcholine mixtures, for the gel → liquid-crystalline phase transition of dipalmitoyl–phosphatidylcholine multilayers, and for a biological membrane, barley thylakoid. This refined assignment offers physically plausible reasoning for the observed phenomena and is able to explain frequency shifts and bandwidth changes observed previously upon lipid phase transitions, including their nonconcerted temperature dependences. In biological membranes, this interpretation allows the separation of protein- and membrane-dynamics-induced lipid conformational changes. © 1999 John Wiley & Sons, Inc. Biospectroscopy 5: 169–178, 1999

模型膜和生物膜中有序和无序脂质脂肪酰基链段对γ - ch2波段的可分离贡献:傅里叶变换红外光谱研究
在本文中,我们重新讨论了脂质分子的ν(C - H)拉伸区。该区域被广泛用于跟踪脂质相变,特别是νsymCH2波段的频移和带宽变化已被用于这方面。在这里,我们提出并证明了在这些现象的背后,在νsymCH2和νasCH2的情况下都存在对分量带。这些对的低频成分被分配到脂肪酰基链反段的CH2基团的振动上,而这些对的高频成分被分配到间扭式链上的CH2基团上。为了证明这些分配,我们已经证明了νCH2频率是脂质脂肪酰基链本身构象的特征,而不是整个脂质基质的状态。曲线拟合实际上揭示了特定的构象成分。利用奇异值分解分析,我们证明了在脂质相变过程中,引起νCH2谱带位移的是各组分的相对强度变化,而不是整个谱带的位移。该方法的结果适用于氘饱和二酰磷脂酰胆碱混合物,二棕榈酰磷脂酰胆碱多层凝胶→液晶相变,以及大麦类囊体生物膜。这种精细的分配为观察到的现象提供了物理上合理的推理,并能够解释之前在脂质相变中观察到的频率变化和带宽变化,包括它们的非协调温度依赖性。在生物膜中,这种解释允许分离蛋白质和膜动力学诱导的脂质构象变化。©1999 John Wiley &儿子,Inc。生物光谱学学报,2009,32 (2):557 - 557
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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