Enhanced and tunable fluorescent quantum dots within a single crystal of protein

被引:0
|
作者
Hui Wei
Stephen House
Jiangjiexing Wu
Jiong Zhang
Zidong Wang
Ying He
Elizabeth J. Gao
Yigui Gao
Howard Robinson
Wei Li
Jianmin Zuo
Ian M. Robertson
Yi Lu
机构
[1] University of Illinois at Urbana-Champaign,Department of Chemistry
[2] University of Illinois at Urbana-Champaign,Department of Materials Science and Engineering
[3] Tianjin University,Key Laboratory for Green Chemical Technology MOE
[4] University of Illinois at Urbana-Champaign,George L. Clark X
[5] Brookhaven National Laboratory,Ray Facility and 3M Materials Laboratory
来源
Nano Research | 2013年 / 6卷
关键词
functional bio-nanomaterials; quantum dots; protein single crystals; X-ray crystallography; tomography;
D O I
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中图分类号
学科分类号
摘要
The design and synthesis of bio-nano hybrid materials can not only provide new materials with novel properties, but also advance our fundamental understanding of interactions between biomolecules and their abiotic counterparts. Here, we report a new approach to achieving such a goal by growing CdS quantum dots (QDs) within single crystals of lysozyme protein. This bio-nano hybrid emitted much stronger red fluorescence than its counterpart without the crystal, and such fluorescence properties could be either enhanced or suppressed by the addition of Ag(I) or Hg(II), respectively. The three-dimensional incorporation of CdS QDs within the lysozyme crystals was revealed by scanning transmission electron microscopy with electron tomography. More importantly, since our approach did not disrupt the crystalline nature of the lysozyme crystals, the metal and protein interactions were able to be studied by X-ray crystallography, thus providing insight into the role of Cd(II) in the CdS QDs formation. [graphic not available: see fulltext]
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页码:627 / 634
页数:7
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