Department of Biological Engineering, Utah State University, Logan, UT 84322, USA.
Mater Sci Eng C Mater Biol Appl. 2013 Jul 1;33(5):3082-4. doi: 10.1016/j.msec.2013.02.011. Epub 2013 Feb 15.
The development of a general approach for non-destructive chemical and biological functionalization of epoxy could expand opportunities for both fundamental studies and creating various device platforms. Epoxy shows unique electrical, mechanical, chemical and biological compatibility and has been widely used for fabricating a variety of devices. Phage display has emerged as a powerful method for selecting peptides that possess enhanced selectivity and binding affinity toward a variety of targets. In this letter, we demonstrate for the first time a powerful yet benign approach for identifying binding motifs to epoxy via comprehensively screened phage displayed peptides. Our results show that the epoxy can be selectively recognized with peptide-displaying phages. Further, along with the development of epoxy-based microstructures; recognition of the epoxy with phage displayed peptides can be specifically localized in these microstructures. We anticipate that these results could open up exciting opportunities in the use of peptide-recognized epoxy in fundamental biochemical recognition studies, as well as in applications ranging from analytical devices, hybrid materials, surface and interface, to cell biology.
发展一种通用的方法,用于对环氧树脂进行非破坏性的化学和生物功能化,可以为基础研究和各种器件平台的创造提供更多机会。环氧树脂具有独特的电学、机械学、化学和生物学兼容性,已被广泛用于制造各种器件。噬菌体展示技术已成为一种强大的方法,用于筛选具有增强的选择性和对各种靶标结合亲和力的肽。在这封信中,我们首次展示了一种强大而良性的方法,通过全面筛选的噬菌体展示肽来鉴定与环氧树脂结合的基序。我们的结果表明,噬菌体展示肽可以选择性地识别环氧树脂。此外,随着环氧树脂基微结构的发展;噬菌体展示肽对环氧树脂的识别可以在这些微结构中特异性地定位。我们预计,这些结果将为在基础生化识别研究以及从分析器件、混合材料、表面和界面到细胞生物学等各个领域中使用肽识别的环氧树脂开辟令人兴奋的机会。