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通过磷-31核磁共振研究人低密度脂蛋白中磷脂和胆固醇的位置及相互作用。

Location and interactions of phospholipid and cholesterol in human low density lipoprotein from 31P nuclear magnetic resonance.

作者信息

Yeagle P L, Martin R B, Pottenger L, Langdon R G

出版信息

Biochemistry. 1978 Jul 11;17(14):2707-10. doi: 10.1021/bi00607a002.

Abstract

The major phospholipids, phosphatidylcholine and spingomyelin, of low density lipoprotein (LDL) are accessible to small amounts of Pr3+, suggesting that the head groups of all mobile phospholipids are on the surface of the particle in contact with the aqueous medium. The major source of the nuclear Overhauser effect enhancement of 31P resonances is the N-methyl proton of the choline moiety, indicating close N-methyl phosphate group interactions, probably similar to those found previously in phospholipid vesicles. This behavior of the phospholipid head groups in LDL is similar to that in small vesicles without cholesterol, suggesting that in LDL most of the cholesterol is not associated with mobile, surface phospholipids. In contrast to LDL, where the presence of a large protein immobilizes some phospholipid head groups, immobilization does not occur in high density lipoprotein, consistent with occurrence of smaller peptides in the latter.

摘要

低密度脂蛋白(LDL)的主要磷脂,即磷脂酰胆碱和鞘磷脂,可与少量Pr3+接触,这表明所有可移动磷脂的头部基团都位于颗粒表面并与水相介质接触。31P共振的核Overhauser效应增强的主要来源是胆碱部分的N-甲基质子,这表明N-甲基磷酸基团之间存在紧密相互作用,可能类似于先前在磷脂囊泡中发现的相互作用。LDL中磷脂头部基团的这种行为与不含胆固醇的小囊泡中的行为相似,这表明在LDL中,大部分胆固醇不与可移动的表面磷脂相关联。与LDL不同,在LDL中大量蛋白质的存在会固定一些磷脂头部基团,而在高密度脂蛋白中则不会发生固定,这与后者中较小肽段的存在情况一致。

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