Protein Design for the Synthesis and Stabilization of Highly Fluorescent Quantum Dots

被引:20
作者
Aires, Antonio [1 ]
Moller, Marco [1 ]
Cortajarena, Aitziber L. [1 ,2 ]
机构
[1] Basque Res & Technol Alliance BRTA, Ctr Cooperat Res Biomat CIC BiomaGUNE, Donostia San Sebastian 20014, Spain
[2] Ikerbasque, Basque Fdn Sci, Bilbao 48013, Spain
基金
欧洲研究理事会;
关键词
METAL-BINDING SITES; IN-VITRO; CDTE; LUMINESCENCE; CDSE; NANOCRYSTALS; COORDINATION; COMPACT; METALLOPROTEINS; SPECIFICITY;
D O I
10.1021/acs.chemmater.0c01484
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Quantum dots (QDs) are presently studied intensively as fluorescent probes for biomedical applications due to their high emission quantum yield, excellent resistance to photobleaching, photostability, and large Stokes shift, when contrasted with commonly utilized organic fluorescent dyes. This study introduces a protein engineering approach to incorporate metal coordination sites for the sustainable synthesis and stabilization of biocompatible CdS QDs in proteins. The resulting protein-stabilized CdS QDs (Prot-QDs), generated by a green aqueous route at 37 degrees C, are highly photoluminescent and photostable, have a long shelf life, and present high stability under physiological conditions. The Prot-QDs showed effective internalization and high fluorescence in cells, even at low doses and biocompatibility. This work focuses on CdS QDs, since this composition has been extensively studied, however this approach could be easily translated to QDs with other metal composition. Here, protein design emerges as a promising approach to generate protein-hybrid nanomaterials as broadly applicable tools in different applications such as light-emitting devices, metal ion detection, and biomedical applications.
引用
收藏
页码:5729 / 5738
页数:10
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