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通过锆介导的 10-巯基癸基膦酸自组装单层在玻璃上的制备和光刻用于蛋白质图案化。

Preparation and photolithography of self-assembled monolayers of 10-mercaptodecanylphosphonic acid on glass mediated by zirconium for protein patterning.

机构信息

National Center for Nanoscience and Technology, 11 Beiyitiao, Zhongguancun, Beijing 100190, PR China.

出版信息

Colloids Surf B Biointerfaces. 2013 Aug 1;108:66-71. doi: 10.1016/j.colsurfb.2013.02.030. Epub 2013 Feb 28.

Abstract

Self-assembled monolayers (SAMs) formed by adsorption of octadecylphosphonic acid (ODPA) on zirconium mediated glass substrates were prepared. In this sandwich structure, Zr(4+) was used as a bi-linker to bind phosphonic acid head group in ODPA to glass substrates. The contact angle of the as-prepared SAMs was measured to be around 104°. X-ray photoelectron spectroscopy (XPS) characterization indicated the modification of Zr(4+) on glass substrates was critical for the formation of reasonably dense, well-ordered SAMs similar in quality to those typically formed on other metal oxide surfaces. Bifunctional molecule, 10-mercaptodecanylphosphonic acid (MDPA), bearing thiol terminal groups for various chemical reactions, was synthesized and formed SAMs on glass using the same approach, which allowed us to control the surface chemistry and functionality through photooxidation of the thiol terminal group. Photopatterning of proteins was performed first by exposing the SAMs to UV light through a mask, followed by protein immobilization to the masked regions through a heterobifunctional linker, while the exposed areas prohibit nonspecific protein absorption. The present strategy, which combined the SAMs assembly and photolithography, offered a facile approach for the fabrication of biomolecule patterning and could be applied to construction of biochips and other applications.

摘要

自组装单分子层(SAMs)通过十八烷基膦酸(ODPA)在锆介导的玻璃基底上吸附制备。在这种三明治结构中,Zr(4+) 被用作双连接剂,将膦酸头基结合到玻璃基底上。所制备的 SAMs 的接触角约为 104°。X 射线光电子能谱(XPS)表征表明,Zr(4+) 在玻璃基底上的修饰对于形成类似于通常在其他金属氧化物表面形成的合理密集、有序的 SAMs 是至关重要的。具有用于各种化学反应的硫醇端基的双官能分子 10-巯基癸基膦酸(MDPA)通过相同的方法在玻璃上形成 SAMs,这允许我们通过硫醇端基的光氧化来控制表面化学和功能。首先通过掩模将 SAMs 暴露于紫外光下来进行蛋白质的光图案化,然后通过异双官能连接剂将蛋白质固定在掩蔽区域,而暴露区域则阻止非特异性蛋白质吸收。这种将 SAMs 组装和光刻相结合的策略提供了一种简便的生物分子图案化制造方法,可应用于生物芯片和其他应用的构建。

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