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基于脂质的纳米盘向单层囊泡的生长动力学——时间分辨小角中子散射(SANS)研究

Growth kinetics of lipid-based nanodiscs to unilamellar vesicles-a time-resolved small angle neutron scattering (SANS) study.

作者信息

Mahabir Suanne, Small Darcy, Li Ming, Wan Wankei, Kučerka Norbert, Littrell Kenneth, Katsaras John, Nieh Mu-Ping

机构信息

The University of Western Ontario, London, Ontario, Canada.

出版信息

Biochim Biophys Acta. 2013 Mar;1828(3):1025-35. doi: 10.1016/j.bbamem.2012.11.002. Epub 2012 Nov 26.

Abstract

Mixtures of dimyristoyl-phosphatidylcholine (DMPC), dimyristoyl-phosphatidylglycerol (DMPG) and dihexanoyl-phosphatidylcholine (DHPC) in aqueous solutions spontaneously form monodisperse, bilayered nanodiscs (also known as "bicelles") at or below the melting transition temperature of DMPC (T(M) ~23°C). In dilute systems above the main transition temperature T(M) of DMPC, bicelles coalesce (increasing their diameter) and eventually self-fold into unilamellar vesicles (ULVs). Time-resolved small angle neutron scattering was used to study the growth kinetics of nanodiscs below and equal to T(M) over a period of hours as a function of temperature at two lipid concentrations in presence or absence of NaCl salt. Bicelles seem to undergo a sudden initial growth phase with increased temperature, which is then followed by a slower reaction-limited growth phase that depends on ionic strength, lipid concentration and temperature. The bicelle interaction energy was derived from the colloidal theory of Derjaguin and Landau, and Verwey and Overbeek (DLVO). While the calculated total energy between discs is attractive and proportional to their growth rate, a more detailed mechanism is proposed to describe the mechanism of disc coalescence. After annealing at low temperature (low-T), samples were heated to 50°C in order to promote the formation of ULVs. Although the low-T annealing of samples has only a marginal effect on the mean size of end-state ULVs, it does affect their polydispersity, which increases with increased T, presumably driven by the entropy of the system.

摘要

在水溶液中,二肉豆蔻酰磷脂酰胆碱(DMPC)、二肉豆蔻酰磷脂酰甘油(DMPG)和二己酰磷脂酰胆碱(DHPC)的混合物在DMPC的熔点转变温度(T(M)~23°C)及以下时会自发形成单分散的双层纳米盘(也称为“双分子层微囊”)。在高于DMPC主要转变温度T(M)的稀溶液体系中,双分子层微囊会合并(直径增大),最终自折叠形成单层囊泡(ULV)。采用时间分辨小角中子散射技术,研究了在有或无NaCl盐存在的情况下,两种脂质浓度下纳米盘在低于和等于T(M)时随温度变化数小时的生长动力学。双分子层微囊似乎在温度升高时经历一个突然的初始生长阶段,随后是一个较慢的反应受限生长阶段,该阶段取决于离子强度、脂质浓度和温度。双分子层微囊的相互作用能源自Derjaguin和Landau以及Verwey和Overbeek(DLVO)的胶体理论。虽然计算出的盘之间的总能量具有吸引力且与它们的生长速率成正比,但我们提出了一个更详细的机制来描述盘合并的机制。在低温(低T)退火后,将样品加热到50°C以促进单层囊泡的形成。尽管样品的低T退火对最终状态单层囊泡的平均尺寸只有很小的影响,但它确实会影响其多分散性,多分散性随温度升高而增加,这可能是由系统的熵驱动的。

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