Enhanced and tunable fluorescent quantum dots within a single crystal of protein |
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Authors: | 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 |
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Affiliation: | 1. Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA 2. Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA 3. Key Laboratory for Green Chemical Technology MOE, Tianjin University, Tianjin, 300072, China 4. George L. Clark X-Ray Facility and 3M Materials Laboratory, University of Illinois at Urbana-Champaign, Urbana, Illinois, 61801, USA 5. Department of Biology, Brookhaven National Laboratory, Upton, New York, 11973, USA
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Abstract: | 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. |
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Keywords: | functionalbio-nanomaterials quantum dots protein single crystals X-ray crystallography tomography |
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