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Thermodynamic thermomechanical and structural properties of a hydrated asymmetric phosphatidylcholine.

机译:水合不对称磷脂酰胆碱的热力学热力学和结构性质。

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摘要

1-Behenyl-2-lauryl-sn-glycero-3-phosphocholine (22/12 PC) belongs to a unique group of phospholipids in which the molecule has one acyl chain almost twice as long as the other. The temperature-composition phase diagram for this lipid in the range of 25-65 degrees C, and 0 to 84.3% (w/w) water has been constructed by using the isoplethal method in the heating direction and x-ray diffraction for phase identification and structure characterization. At water contents between 10.3 and 34% (w/w) and at temperatures below 43 degrees C, a single mixed interdigitated lamellar gel phase (Lm beta, [symbol: see text]) of the type described by Hui et al. (1984. Biochemistry. 23:5570-5577) and McIntosh et al. (1984. Biochemistry. 23:4038-4044) was found. A second phase consisting of bulk aqueous solution coexists with the Lm beta phase at hydration levels above 34% (w/w) water in the temperature range between 25 and 43 degrees C. Above 43 degrees C, a partially interdigitated lamellar liquid crystalline (Lp alpha) phase ([symbol: see text]) is seen in the water concentration range extending from 0 to 84.3% (w/w). The pure Lp alpha phase is found below 43% (w/w) water, while coexistence of the Lp alpha phase and the bulk aqueous solution is observed above this water concentration which marks the hydration boundary. Interestingly, the latter boundary for both Lm beta and Lp alpha phases is nearly vertical in the temperature range studied. Furthermore, the lamellar chain-melting transition temperature appears to be relatively insensitive to hydration in the range 0-85% (w/w) water. We have confirmed the identify of the Lm beta phase by constructing a 5.7-A resolution electron density profile on oriented samples by the swelling method. Temperature-induced chain melting effects an increase in lipid bilayer thickness suggesting that the Lp alpha phase has chains packed in the partially as opposed to the mixed interdigitated configuration. Unlike the symmetric phosphatidylcholines a ripple (P beta') phase was not found as an intermediate between the low and high temperature lamellar phases of 22/12 PC. The specific volume of 22/12 PC is 940 (+/- 1) microliter/g and 946 (+/- 1) microliter/g in the hydrated lamellar gel state at 28 (+/- 2) and 40 (+/- 2) degrees C, respectively, from neutral buoyancy experiments. Based on measurements of the temperature dependence of the various lattice parameters of the different phases encountered in this study the corresponding lattice thermal expansion coefficients have been measured. These are discussed and their dependence on lipid hydration is reported.
机译:1-苯甲基-2-月桂基-sn-甘油-3-磷酸胆碱(22/12 PC)属于独特的磷脂基团,其中该分子的一个酰基链的长度几乎是另一个的两倍。该脂质的温度组成相图在25-65摄氏度范围内,水的含量为0至84.3%(w / w),这是通过在加热方向上使用等渗方法和X射线衍射进行的,以进行相鉴定和结构表征。 Hui等人在水含量在10.3%至34%(w / w)之间且温度低于43摄氏度时,形成了一个混合的交错指状层状凝胶相(Lm beta,[符号:参见文字])。 (1984. Biochemistry。23:5570-5577)和McIntosh等。 (1984.Biochemistry.23:4038-4044)被发现。在25至43摄氏度之间的温度范围内,水相含量高于34%(w / w)时,由本体水溶液组成的第二相与Lmβ相共存。高于43摄氏度时,部分交指的层状液晶(Lp在水浓度范围从0到84.3%(w / w)的范围内可以看到α)相([符号:参见文字])。发现纯Lpα相的水含量低于43%(w / w),而在该水浓度以上(表明水合边界)时,观察到Lpα相和本体水溶液的共存。有趣的是,在所研究的温度范围内,Lmβ和Lpα相的后一个边界几乎是垂直的。此外,在0-85%(w / w)水的范围内,层状链熔融转变温度似乎对水合相对不敏感。我们已经通过溶胀法在定向样品上构建了5.7-A分辨率的电子密度分布图,从而确定了Lmβ相的鉴定。温度诱导的链熔化影响脂质双层厚度的增加,表明Lpα相的链部分混合,而不是混合的叉指结构。与对称的磷脂酰胆碱不同,没有发现波纹(P beta')相作为22/12 PC的低温和高温层状相之间的中间产物。在水合层状凝胶状态下,在28(+/- 2)和40(+/-)的水合层状凝胶状态下,22/12 PC的比容为940(+/- 1)微升/克和946(+/- 1)微升/克。 2)分别来自中性浮力实验的摄氏度。基于对本研究中遇到的不同相的各种晶格参数的温度依赖性的测量,已经测量了相应的晶格热膨胀系数。讨论了这些,并报道了它们对脂质水合作用的依赖性。

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