Mao Chuanbin, Flynn Christine E, Hayhurst Andrew, Sweeney Rozamond, Qi Jifa, Georgiou George, Iverson Brent, Belcher Angela M
Department of Chemistry and Biochemistry, Institute for Cellular and Molecular Biology, Center for Nano- and Molecular Science and Technology, and Texas Materials Institute, University of Texas, Austin, TX 78712, USA.
Proc Natl Acad Sci U S A. 2003 Jun 10;100(12):6946-51. doi: 10.1073/pnas.0832310100. Epub 2003 May 30.
The highly organized structure of M13 bacteriophage was used as an evolved biological template for the nucleation and orientation of semiconductor nanowires. To create this organized template, peptides were selected by using a pIII phage display library for their ability to nucleate ZnS or CdS nanocrystals. The successful peptides were expressed as pVIII fusion proteins into the crystalline capsid of the virus. The engineered viruses were exposed to semiconductor precursor solutions, and the resultant nanocrystals that were templated along the viruses to form nanowires were extensively characterized by using high-resolution analytical electron microscopy and photoluminescence. ZnS nanocrystals were well crystallized on the viral capsid in a hexagonal wurtzite or a cubic zinc blende structure, depending on the peptide expressed on the viral capsid. Electron diffraction patterns showed single-crystal type behavior from a polynanocrystalline area of the nanowire formed, suggesting that the nanocrystals on the virus were preferentially oriented with their [001] perpendicular to the viral surface. Peptides that specifically directed CdS nanocrystal growth were also engineered into the viral capsid to create wurtzite CdS virus-based nanowires. Lastly, heterostructured nucleation was achieved with a dual-peptide virus engineered to express two distinct peptides within the same viral capsid. This work represents a genetically controlled biological synthesis route to a semiconductor nanoscale heterostructure.
M13噬菌体高度有序的结构被用作半导体纳米线成核和取向的进化生物模板。为了创建这种有序模板,通过使用pIII噬菌体展示文库,根据肽使ZnS或CdS纳米晶体成核的能力来选择肽。成功的肽被表达为pVIII融合蛋白,进入病毒的结晶衣壳。将工程病毒暴露于半导体前驱体溶液中,利用高分辨率分析电子显微镜和光致发光对沿病毒模板化形成纳米线的所得纳米晶体进行了广泛表征。根据病毒衣壳上表达的肽,ZnS纳米晶体在病毒衣壳上以六方纤锌矿或立方闪锌矿结构良好结晶。电子衍射图谱显示,形成的纳米线的多纳米晶体区域呈现单晶型行为,这表明病毒上的纳米晶体优先以其[001]垂直于病毒表面的方向取向。还将特异性指导CdS纳米晶体生长的肽工程化到病毒衣壳中,以创建基于纤锌矿CdS病毒的纳米线。最后,通过在同一病毒衣壳内表达两种不同肽的双肽病毒实现了异质结构成核。这项工作代表了一种基因控制的生物合成路线,用于制备半导体纳米级异质结构。