Espinoza Luis A Tercero, Schumann Kate R, Luk Yan-Yeung, Israel Barbara A, Abbott Nicholas L
Department of Chemical and Biological Engineering, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Langmuir. 2004 Mar 16;20(6):2375-85. doi: 10.1021/la035774i.
We report the orientational behavior of nematic phases of 4-cyano-4'-pentylbiphenyl (5CB) on cationic, anionic, and nonionic surfaces before and after contact of these surfaces with solutions containing the negatively charged vesicular stomatitis virus (VSV). The surfaces were prepared on evaporated films of gold by either adsorption of poly-L-lysine (cationic) or formation of self-assembled monolayers (SAMs) from HS(CH2)2SO3- (anionic) or HS(CH2)11(OCH2CH2)4OH (nonionic). Prior to treatment with virus, we measured the initial orientation of 5CB (delta epsilon = epsilon(parallel) - epsilon(perpendicular) > 0) to be parallel to the cationic surfaces (planar anchoring) but perpendicular (homeotropic) after equilibration for 5 days. A similar transition from planar to homeotropic orientation of 5CB was observed on the anionic surfaces. Only planar orientations of 5CB were observed on the nonionic surfaces. Because N-(4-methoxybenzylidene)-4-butylaniline (MBBA, delta epsilon = epsilon(parallel) - epsilon(perpendicular) < 0) exhibited planar alignment on all surfaces, the time-dependent alignment of 5CB on the ionic surfaces is consistent with a dipolar coupling between the 5CB and electrical double layers formed at the ionic interfaces. Treatment ofpoly-L-lysine-coated gold films (cationic) with purified solutions of VSV containing 10(8)-10(10) plaque-forming units per milliliter (pfu/mL) led to the homeotropic alignment of 5CB immediately after contact of 5CB with the surface. In contrast, treatment of anionic surfaces and nonionic surfaces with solutions of VSV containing approximately 10(10) pfu/mL did not cause immediate homeotropic alignment of 5CB. These results and others suggest that homeotropic alignment of 5CB on cationic surfaces treated with VSV of titer > or = 10(8) pfu/mL reflects the presence of virus electrostatically bound to these surfaces.
我们报告了4-氰基-4'-戊基联苯(5CB)向列相在阳离子、阴离子和非离子表面上的取向行为,这些表面在与含有带负电荷的水泡性口炎病毒(VSV)的溶液接触之前和之后的情况。通过吸附聚-L-赖氨酸(阳离子)或由HS(CH2)2SO3-(阴离子)或HS(CH2)11(OCH2CH2)4OH(非离子)形成自组装单分子层(SAMs),在蒸发的金膜上制备这些表面。在用病毒处理之前,我们测量到5CB(δε = ε(平行) - ε(垂直) > 0)的初始取向与阳离子表面平行(平面锚定),但在平衡5天后变为垂直(垂面取向)。在阴离子表面上也观察到了5CB从平面取向到垂面取向的类似转变。在非离子表面上只观察到5CB的平面取向。因为N-(4-甲氧基亚苄基)-4-丁基苯胺(MBBA,δε = ε(平行) - ε(垂直) < 0)在所有表面上都表现出平面排列,所以5CB在离子表面上随时间的排列与5CB和在离子界面形成的双电层之间的偶极耦合一致。用每毫升含有10(8)-10(10)个空斑形成单位(pfu/mL)的VSV纯化溶液处理聚-L-赖氨酸包被的金膜(阳离子),导致5CB与表面接触后立即出现垂面排列。相比之下,用含有约10(10) pfu/mL的VSV溶液处理阴离子表面和非离子表面,并没有立即导致5CB的垂面排列。这些结果以及其他结果表明,用滴度≥10(8) pfu/mL的VSV处理阳离子表面时,5CB的垂面排列反映了静电结合在这些表面上的病毒的存在。