Lee Ki-Bum, Park So-Jung, Mirkin Chad A, Smith Jennifer C, Mrksich Milan
Northwestern University, Department of Chemistry and Center for Nanofabrication and Molecular Self-Assembly, 2145 Sheridan Road, Evanston, IL 60208, USA.
Science. 2002 Mar 1;295(5560):1702-5. doi: 10.1126/science.1067172. Epub 2002 Feb 7.
Dip-pen nanolithography was used to construct arrays of proteins with 100- to 350-nanometer features. These nanoarrays exhibit almost no detectable nonspecific binding of proteins to their passivated portions even in complex mixtures of proteins, and therefore provide the opportunity to study a variety of surface-mediated biological recognition processes. For example, reactions involving the protein features and antigens in complex solutions can be screened easily by atomic force microscopy. As further proof-of-concept, these arrays were used to study cellular adhesion at the submicrometer scale.
浸笔光刻技术被用于构建具有100至350纳米特征的蛋白质阵列。这些纳米阵列即使在复杂的蛋白质混合物中,其钝化部分也几乎没有可检测到的蛋白质非特异性结合,因此为研究各种表面介导的生物识别过程提供了机会。例如,通过原子力显微镜可以轻松筛选涉及复杂溶液中蛋白质特征和抗原的反应。作为进一步的概念验证,这些阵列被用于研究亚微米尺度下的细胞粘附。