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利用自组装单分子层来理解人造表面与蛋白质和细胞之间的相互作用。

Using self-assembled monolayers to understand the interactions of man-made surfaces with proteins and cells.

作者信息

Mrksich M, Whitesides G M

机构信息

Department of Chemistry, Harvard University, Cambridge, Massachusetts 02138, USA.

出版信息

Annu Rev Biophys Biomol Struct. 1996;25:55-78. doi: 10.1146/annurev.bb.25.060196.000415.

Abstract

Self-assembled monolayers (SAMs) formed on the adsorption of long-chain alkanethiols to the surface of gold or alkylsilanes to hydroxylated surfaces are well-ordered organic surfaces that permit control over the properties of the interface at the molecular scale. The ability to present molecules, peptides, and proteins at the interface make SAMs especially useful for fundamental studies of protein adsorption and cell adhesion. Microcontact printing is a simple technique that can pattern the formation of SAMs in the plane of the monolayer with dimensions on the micron scale. The convenience and broad application offered by SAMs and microcontact printing make this combination of techniques useful for studying a variety of fundamental phenomena in biointerfacial science.

摘要

通过长链烷硫醇吸附到金表面或烷基硅烷吸附到羟基化表面形成的自组装单分子层(SAMs)是有序的有机表面,能够在分子尺度上控制界面性质。在界面处呈现分子、肽和蛋白质的能力使SAMs在蛋白质吸附和细胞黏附的基础研究中特别有用。微接触印刷是一种简单的技术,可以在单分子层平面上以微米尺度的尺寸对SAMs的形成进行图案化。SAMs和微接触印刷所提供的便利性和广泛应用使这种技术组合对于研究生物界面科学中的各种基本现象很有用。

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