Jin Hyo-Eon, Lee Seung-Wuk
Department of Bioengineering, University of California, Berkeley, Berkeley, CA, USA.
Biological Systems and Engineering, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Methods Mol Biol. 2018;1776:487-502. doi: 10.1007/978-1-4939-7808-3_32.
M13 bacteriophages have several qualities that make them attractive candidates as building blocks for tissue regenerating scaffold materials. Through genetic engineering, a high density of functional peptides and proteins can be simultaneously displayed on the M13 bacteriophage's outer coat proteins. The resulting phage can self-assemble into nanofibrous network structures and can guide the tissue morphogenesis through proliferation, differentiation and apoptosis. In this manuscript, we will describe methods to develop major coat-engineered M13 phages as a basic building block and aligned tissue-like matrices to develop regenerative nanomaterials.
M13噬菌体具有多种特性,使其成为组织再生支架材料构建模块的理想候选者。通过基因工程,可以在M13噬菌体的外衣蛋白上同时高密度展示功能肽和蛋白质。产生的噬菌体可以自组装成纳米纤维网络结构,并通过增殖、分化和凋亡来引导组织形态发生。在本手稿中,我们将描述开发主要衣壳工程化M13噬菌体作为基本构建模块以及排列成组织样基质以开发再生纳米材料的方法。