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利用原子力显微镜研究玻璃上的囊泡吸附和脂质双层形成。

Vesicle adsorption and lipid bilayer formation on glass studied by atomic force microscopy.

作者信息

Schönherr Holger, Johnson Joseph M, Lenz Peter, Frank Curtis W, Boxer Steven G

机构信息

NSF MRSEC Center on Polymer Interfaces and Macromolecular Assemblies (CPIMA), Stanford University, Stanford, California 94305-5025, USA.

出版信息

Langmuir. 2004 Dec 21;20(26):11600-6. doi: 10.1021/la049302v.

Abstract

The adsorption of phosphatidylcholine (PC) vesicles (30, 50, and 100 nm nominal diameters) and of dye-labeled PC vesicles (labeled with 6% Texas Red fluorophore (TR) and encapsulated carboxy fluorescein (CF)) to glass surfaces was studied by contact mode atomic force microscopy in aqueous buffer. These studies were performed in part to unravel details of the previously observed isolated rupture of dye-labeled PC vesicles on glass (Johnson, J. M.; Ha, T.; Chu, S.; Boxer, S. G. Biophys. J. 2002, 83, 3371-3379), specifically to differentiate partial rupture, that is, pore formation and leakage of entrapped dye, from full rupture to form bilayer disks. In addition, the adhesion potential of PC vesicles on glass was calculated based upon the adhesion-driven flattening of adsorbed vesicles and a newly developed theoretical model. The vesicles were found to flatten considerably upon adsorption to glass (width-to-height ratio of approximately 5), which leads to an estimate for the adhesion potential and for the critical rupture radius of 1.5 x 10(-4) J/m2 and 250 nm, respectively. Independent of vesicle size and loading with dye molecules, the adsorption of intact vesicles was observed at all concentrations below a threshold concentration, above which the formation of smooth lipid bilayers occurred. In conjunction with previous work (Johnson, J. M.; Ha, T.; Chu, S.; Boxer, S. G. Biophys. J. 2002, 83, 3371-3379), these data show that 6% TR 20 mM CF vesicles adsorb to the surface intact but undergo partial rupture in which they exchange content with the external buffer.

摘要

通过接触模式原子力显微镜在水性缓冲液中研究了磷脂酰胆碱(PC)囊泡(标称直径为30、50和100 nm)以及染料标记的PC囊泡(用6%德克萨斯红荧光团(TR)标记并包裹羧基荧光素(CF))在玻璃表面的吸附情况。进行这些研究的部分目的是揭示先前观察到的染料标记的PC囊泡在玻璃上的孤立破裂细节(约翰逊,J.M.;哈,T.;朱,S.;博克瑟,S.G.《生物物理杂志》2002年,83卷,3371 - 3379页),特别是区分部分破裂,即孔形成和包封染料的泄漏,与完全破裂形成双层盘。此外,基于吸附囊泡的粘附驱动扁平化以及新开发的理论模型计算了PC囊泡在玻璃上的粘附势。发现囊泡在吸附到玻璃上时会显著扁平化(宽高比约为5),这分别导致粘附势和临界破裂半径的估计值为1.5×10⁻⁴ J/m²和250 nm。与囊泡大小和染料分子负载无关,在低于阈值浓度的所有浓度下都观察到完整囊泡的吸附,高于该阈值浓度则会形成光滑的脂质双层。结合先前的工作(约翰逊,J.M.;哈,T.;朱,S.;博克瑟,S.G.《生物物理杂志》2002年,83卷,3371 - 3379页),这些数据表明6%TR 20 mM CF囊泡完整地吸附到表面,但会经历部分破裂,在此过程中它们与外部缓冲液交换内容物。

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