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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Lysozyme Adsorption Studies at the Silica/Water Interface Using Dual Polarization Interferometry
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Lysozyme Adsorption Studies at the Silica/Water Interface Using Dual Polarization Interferometry

机译:二氧化硅/水界面上的溶菌酶吸附的双极化干涉法研究

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摘要

Lysozyme adsorption at the silica/water interface has been studied using a new analytical technique called dual polarization interferometry.This laboratory-based technique allows the build up or removal of molecular layers adsorbing or reacting on a lightly doped silicon dioxide(silica)surface to be measured in terms of thickness and refractive index changes with time.Lysozyme adsorption was studied at a range of concentrations from 0.03 to 4.0 g dm~(-3) and at both pH 4 and pH 7.Adsorbed layers ranging from 14 to 43 1 A in thickness and 0.21 to 2.36(+-)0.05 mg m~(-2) in mass coverage were observed at pH 4 with increasing lysozyme concentration,indicating a strong deformation of the monolayer over the low concentration range and the formation of an almost complete sideways-on bilayer toward the high concentration of 4 g dm~(-3).At pH 7,the thickness of adsorbed layers varied from 16 to 541 A with significantly higher surface coverage(0.74 to 3.29(+-)0.05 mg m~(-2),again indicating structural deformation during the initial monolayer formation,followed by a gradual transition to bilayer adsorption over the high concentration end.The pH recycling performed at a fixed lysozyme concentration of 1.0 g dm~(-3) indicated a broadly reversible adsorption regardless of whether the pH was cycled from pH 7 to pH 4 and back again or vice versa.These observations are in good agreement with earlier studies undertaken using neutron reflection although the fine details of molecular orientations in the layers differ subtly.
机译:二氧化硅/水界面上的溶菌酶吸附已使用一种称为双极化干涉法的新分析技术进行了研究,这种基于实验室的技术允许在轻掺杂二氧化硅(silica)表面上形成或去除吸附或反应的分子层。在0.03至4.0 g dm〜(-3)的浓度范围内以及在pH 4和pH 7的条件下研究了溶菌酶的吸附。吸附层的范围为14至43 1 A随着溶菌酶浓度的增加,在pH 4时观察到厚度为0.21至2.36(+-)0.05 mg m〜(-2)的质量覆盖率,表明在低浓度范围内单层的强烈变形并形成了几乎完整的在高浓度4 g dm〜(-3)的情况下向侧面倾斜双层。在pH值为7时,吸附层的厚度从16到541 A不等,表面覆盖率明显更高(0.74到3.29(+-)0.05 mg m〜 (-2),再次表示结构在初始单层形成过程中发生结构变形,随后在高浓度端逐渐过渡到双层吸附。在1.0 g dm〜(-3)的固定溶菌酶浓度下进行的pH回收表明,无论pH值是否均可以广泛逆转吸附这些观测值与pH值从7循环到pH 4并再次返回,反之亦然。这些观察结果与早期使用中子反射进行的研究非常吻合,尽管各层中分子取向的细微差别有所不同。

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