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水合二肉豆蔻酰卵磷脂结构的温度和成分依赖性

Temperature and compositional dependence of the structure of hydrated dimyristoyl lecithin.

作者信息

Janiak M J, Small D M, Shipley G G

出版信息

J Biol Chem. 1979 Jul 10;254(13):6068-78.

PMID:447695
Abstract

Differential scanning calorimetry and x-ray diffraction techniques have been used to investigate the structure and phase behavior of hydrated dimyristoyl lecithin (DML) in the hydration range 7.5 to 60 weight % water and the temperature range -10 to +60 degrees C. Four different calorimetric transitions have been observed: T1, a low enthalpy transition (deltaH approximately equal to 1 kcal/mol of DML) at 0 degrees C between lamellar phases (L leads to Lbeta); T2, the low enthalpy "pretransition" at water contents greater than 20 weight % corresponding to the transition Lbeta leads to Pbeta; T3, the hydrocarbon chain order-disorder transition (deltaH = 6 to 7 kcal/mol of DML) representing the transition of the more ordered low temperature phases (Lbeta, Pbeta, or crystal C, depending on the water content) to the lamellar Lalpha phase; T4, a transition occurring at 25--27 degrees C at low water contents representing the transition from the lamellar Lbeta phase to a hydrated crystalline phase C. The structures of the Lbeta, Pbeta, C, and Lalpha phases have been examined as a function of temperature and water content. The Lbeta structure has a lamellar bilayer organization with the hydrocarbon chains fully extended and tilted with respect to the normal to the bilayer plane, but packed in a distorted quasihexagonal lattice. The Pbeta structure consists of lipid bilayer lamellae distorted by a periodic "ripple" in the plane of the lamellae; the hydrocarbon chains are tilted but appear to be packed in a regular hexagonal lattice. The diffraction pattern from the crystalline phase C indexes according to an orthorhombic cell with a = 53.8 A, b = 9.33 A, c = 8.82 A. In the lamellae bilayer Lalpha strucure, the hydrocarbon chains adopt a liquid-like conformation. Analysis of the hydration characteristics and bilayer parameters (lipid thickness, surface area/molecule) of synthetic lecithins permits an evaluation of the generalized hydration and structural behavior of this class of lipids.

摘要

差示扫描量热法和X射线衍射技术已被用于研究水合度在7.5至60重量%水以及温度范围在-10至+60摄氏度内的水合二肉豆蔻酰卵磷脂(DML)的结构和相行为。观察到了四种不同的量热转变:T1,在0摄氏度时层状相之间(L转变为Lβ)的低焓转变(ΔH约等于1千卡/摩尔DML);T2,在水含量大于20重量%时的低焓“预转变”,对应于Lβ转变为Pβ;T3,烃链有序-无序转变(ΔH = 6至7千卡/摩尔DML),代表更有序的低温相(Lβ、Pβ或晶体C,取决于水含量)转变为层状Lα相;T4,在低水含量下于25 - 27摄氏度发生的转变,代表从层状Lβ相转变为水合结晶相C。已研究了Lβ、Pβ、C和Lα相的结构随温度和水含量的变化。Lβ结构具有层状双分子层组织,烃链完全伸展并相对于双分子层平面的法线倾斜,但堆积在扭曲的准六边形晶格中。Pβ结构由脂质双分子层薄片组成,薄片平面内存在周期性“波纹”使其扭曲;烃链倾斜但似乎堆积在规则的六边形晶格中。结晶相C的衍射图谱根据一个正交晶胞进行指标化,a = 53.8 Å,b = 9.33 Å,c = 8.82 Å。在层状双分子层Lα结构中,烃链呈现类似液体的构象。对合成卵磷脂的水合特性和双分子层参数(脂质厚度、分子表面积)的分析有助于评估这类脂质的一般水合和结构行为。

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