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天然富含乙酰胆碱受体的膜中蛋白质 - 脂质界面处磷脂和甾醇离散位点的揭示。

Disclosure of discrete sites for phospholipid and sterols at the protein-lipid interface in native acetylcholine receptor-rich membrane.

作者信息

Antollini S S, Barrantes F J

机构信息

Instituto de Investigaciones Bioquímicas de Bahía Blanca, Argentina.

出版信息

Biochemistry. 1998 Nov 24;37(47):16653-62. doi: 10.1021/bi9808215.

Abstract

There is an increasing body of evidence to support the notion that the function of the nicotinic acetylcholine receptor (AChR) is influenced by its lipid microenvironment [see Barrantes, F. J. (1993) FASEB J. 7, 1460-1467]. We have recently made use of the so-called generalized polarization (GP) of the fluorescent probe Laurdan (6-dodecanoyl-2-(dimethylamino)naphthalene) to learn about the physical state of the lipids in Torpedo marmorata AChR native membrane [Antollini, S. S., Soto, M. A., Bonini de Romanelli, I., Gutiérrez Merino, C., Sotomayor, P., and Barrantes, F. J. (1996) Biophys. J. 70, 1275-1284] and cells expressing endogenous or heterologous AChR [Zanello, L. P., Aztiria, E., Antollini, S., and Barrantes, F. J. (1996) Biophys. J. 70, 2155-2164]. In the present work, Laurdan GP was measured in T. marmorata native AChR membrane by direct excitation or under energy transfer conditions in the presence of exogenous lipids. GP was found to diminish in these two regions upon addition of oleic acid and dioleoylphosphatidylcholine and not to vary significantly upon addition of cholesterol hemisuccinate, indicating an increase in the polarity of the single, ordered-liquid lipid phase in the two former cases. Complementary information about the bulk lipid order was obtained from measurements of fluorescence anisotropy of DPH and two of its derivatives. The membrane order diminished in the presence of oleic acid and dioleoylphosphatidylcholine. The location of Laurdan was determined using the parallax method. Laurdan lies at approximately 10 A from the center of the bilayer, i.e., at depth of approximately 5 A from the lipid-water interface. Exogenous lipids modified the energy transfer efficiency from the intrinsic fluorescence to Laurdan. This strategy is introduced as a new analytic tool that discloses for the first time the occurrence of discrete and independent sites for phospholipids and sterols, respectively, both accessible to fatty acids, and presumably located at a shallow depth close to the phospholipid polar head region in the native AChR membrane.

摘要

越来越多的证据支持这样一种观点,即烟碱型乙酰胆碱受体(AChR)的功能受其脂质微环境的影响[见Barrantes, F. J.(1993年)《美国实验生物学会联合会杂志》7, 1460 - 1467]。我们最近利用荧光探针劳丹(6 - 十二烷酰基 - 2 -(二甲基氨基)萘)的所谓广义极化(GP)来了解电鳐AChR天然膜中脂质的物理状态[Antollini, S. S., Soto, M. A., Bonini de Romanelli, I., Gutiérrez Merino, C., Sotomayor, P., 和Barrantes, F. J.(1996年)《生物物理学杂志》70, 1275 - 1284]以及表达内源性或异源性AChR的细胞[Zanello, L. P., Aztiria, E., Antollini, S., 和Barrantes, F. J.(1996年)《生物物理学杂志》70, 2155 - 2164]。在本研究中,通过直接激发或在存在外源性脂质的能量转移条件下,测量了电鳐天然AChR膜中的劳丹GP。发现添加油酸和二油酰磷脂酰胆碱后,这两个区域的GP降低,而添加胆固醇半琥珀酸酯后没有显著变化,这表明在前两种情况下,单一的有序液态脂质相的极性增加。通过测量DPH及其两种衍生物的荧光各向异性,获得了关于整体脂质有序性的补充信息。在油酸和二油酰磷脂酰胆碱存在下,膜的有序性降低。使用视差法确定了劳丹的位置。劳丹位于距双层中心约10埃处,即距脂质 - 水界面约5埃的深度。外源性脂质改变了从固有荧光到劳丹的能量转移效率。这种策略作为一种新的分析工具被引入,它首次揭示了分别存在磷脂和甾醇的离散且独立的位点,这两个位点都可被脂肪酸接近,并且可能位于天然AChR膜中靠近磷脂极性头部区域的浅深度处。

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