Chung Woo-Jae, Lee Doe-Young, Yoo So Young
College of Biotechnology and Bioengineering, Sungkyunkwan University, Suwon, Republic of Korea.
BIO-IT Foundry Technology Institute, Pusan National University, Busan, Republic of Korea ; Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan, Republic of Korea.
Int J Nanomedicine. 2014 Dec 12;9:5825-36. doi: 10.2147/IJN.S73883. eCollection 2014.
M13 bacteriophage (phage) has emerged as an attractive bionanomaterial owing to its genetically tunable surface chemistry and its potential to self-assemble into hierarchical structures. Furthermore, because of its unique nanoscopic structure, phage has been proposed as a model system in soft condensed physics and as a biomimetic building block for structured functional materials. Genetic engineering of phage provides great opportunities to develop novel nanomaterials with functional surface peptide motifs; however, this biological approach is generally limited to peptides containing the 20 natural amino acids. To extend the scope of phage applications, strategies involving chemical modification have been employed to incorporate a wider range of functional groups, including synthetic chemical compounds. In this review, we introduce the design of chemoselective phage functionalization and discuss how such a strategy is combined with genetic engineering for a variety of medical applications, as reported in recent literature.
M13噬菌体因其可遗传调控的表面化学性质以及自组装成层次结构的潜力,已成为一种具有吸引力的生物纳米材料。此外,由于其独特的纳米结构,噬菌体已被提议作为软凝聚态物理中的一个模型系统以及结构化功能材料的仿生构建块。噬菌体的基因工程为开发具有功能性表面肽基序的新型纳米材料提供了巨大机遇;然而,这种生物学方法通常仅限于含有20种天然氨基酸的肽。为了扩展噬菌体的应用范围,已采用涉及化学修饰的策略来引入更广泛的官能团,包括合成化合物。在本综述中,我们介绍了化学选择性噬菌体功能化的设计,并讨论了如近期文献所报道的,这种策略如何与基因工程相结合用于各种医学应用。