Hyman Paul
Department of Biology, Ashland University, Ashland, Ohio, USA.
Adv Appl Microbiol. 2012;78:55-73. doi: 10.1016/B978-0-12-394805-2.00003-8.
Although people taking different approaches in the field of nanotechnology may target different size ranges, broadly, nanotechnology has the goal of creating structures in the 1-100 nm size range. This is the same size range that bacteriophages synthesize capsids. Bacteriophages also have the desirable property of self-fabrication or self-assembly--much of capsid structural assembly information is a function of the capsid proteins themselves rather than requiring other proteins. This would seem to make bacteriophage protein-based materials ideal for some nanotechnology applications. So far, the majority of research has taken one of two approaches: first, using filamentous bacteriophage display techniques to identify inorganic nanocrystal-binding peptides and using those peptides and the filamentous phage virions to create novel materials, and second, using a variety of bacteriophage and bacteriophage receptor-binding proteins to functionalize surfaces to create biosensors for bacterial detection. Here, I review these two approaches and speculate on some of the challenges for further development of bacteriophage protein-based self-assembling nanomaterials.
尽管在纳米技术领域采用不同方法的人可能针对不同的尺寸范围,但广义而言,纳米技术的目标是制造尺寸在1至100纳米范围内的结构。这与噬菌体合成衣壳的尺寸范围相同。噬菌体还具有自我制造或自组装的理想特性——衣壳结构组装的大部分信息是衣壳蛋白本身的功能,而不需要其他蛋白质。这似乎使基于噬菌体蛋白的材料成为某些纳米技术应用的理想选择。到目前为止,大多数研究采用了以下两种方法之一:第一,使用丝状噬菌体展示技术来鉴定无机纳米晶体结合肽,并使用这些肽和丝状噬菌体病毒粒子来制造新型材料;第二,使用各种噬菌体和噬菌体受体结合蛋白对表面进行功能化,以创建用于细菌检测的生物传感器。在此,我将回顾这两种方法,并推测基于噬菌体蛋白的自组装纳米材料进一步发展面临的一些挑战。