Dipartimento di Chimica e Tecnologie del Farmaco, Sapienza Università di Roma, P.le Aldo Moro 5, 00185 Rome, Italy.
Anal Bioanal Chem. 2010 Oct;398(4):1545-64. doi: 10.1007/s00216-010-3708-6. Epub 2010 Apr 23.
Self-assembled monolayers (SAMs) provide a convenient, flexible and simple system to tailor the interfacial properties of metals, metal oxides and semiconductors. Monomolecular films prepared by self-assembly are attractive for several exciting applications because of the unique possibility of making the selection of different types of terminal functional groups and as emerging tools for nanoscale observation of biological interactions. The tenability of SAMs as platforms for preparing biosurfaces is reviewed and critically discussed. The different immobilization approaches used for anchoring proteins to SAMs are considered as well as the nature of SAMs; particular emphasis is placed on the chemical specificity of protein attachment in view of preserving protein native structure necessary for its functionality. Regarding this aspect, particular attention is devoted to the relation between the immobilization process and the electrochemical response (i.e. electron transfer) of redox proteins, a field where SAMs have attracted remarkable attention as model systems for the design of electronic devices. Strategies for creating protein patterns on SAMs are also outlined, with an outlook on promising and challenging future directions for protein biochip research and applications.
自组装单分子层(SAMs)为调整金属、金属氧化物和半导体的界面性质提供了一种便捷、灵活和简单的系统。通过自组装制备的单分子膜因其独特的选择不同类型的末端官能团的可能性以及作为生物相互作用纳米级观察的新兴工具而受到关注。本文综述并批判性地讨论了 SAMs 作为制备生物表面的平台的可调性。考虑了用于将蛋白质固定到 SAM 上的不同固定化方法以及 SAM 的性质;特别强调了考虑到保持蛋白质功能所必需的天然结构,蛋白质附着的化学特异性。关于这一方面,特别关注固定化过程与氧化还原蛋白质的电化学响应(即电子转移)之间的关系,在这一领域,SAM 作为电子器件设计的模型系统引起了人们的极大关注。还概述了在 SAM 上创建蛋白质图案的策略,并展望了蛋白质生物芯片研究和应用的有前途和具有挑战性的未来方向。