The modification of quantum dot probes used for the targeted imaging of his-tagged fusion proteins

被引:53
作者
Bae, Pan K. [1 ]
Kim, Kyung N. [1 ]
Lee, Seung J. [1 ]
Chang, Hyun J. [1 ]
Lee, Chong K. [2 ]
Park, Joung K. [1 ]
机构
[1] Korea Res Inst Chem Technol, Adv Mat Div, Fus Biotechnol Res Ctr, Taejon 305600, South Korea
[2] Korea Res Inst Chem Technol, Drug Discovery Div, Ctr Antiinfect Agents Res, Taejon 305600, South Korea
关键词
CdTe; Quantum dot; Nickel; Bio-imaging; GREEN-FLUORESCENT PROTEIN; CDSE NANOCRYSTALS; THYMIDINE KINASE; SEMICONDUCTORS; LOCALIZATION; STABILITY; PEPTIDES; CHELATE; CELLS; CDTE;
D O I
10.1016/j.biomaterials.2008.10.049
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In molecular biology and protein detection the immobilized metal ion clusters using a NTA-chelator is a powerful technique in identification and isolation of histidine-tagged fusion proteins. The Oligohistidine tag should serve as a high affinity binding sequence for the purification of any fusion protein via metal chelating adsorbents. We described the preparation and characterization of bioinorganic conjugates made with highly luminescent semiconductor CdTe-CdS core-shell quantum dots (QDs) for biological labeling. A biocompatible surface-functionalized nanoparticle was designed to sense histidine-tagged fusion proteins. This study demonstrates the synthesis of Ni-NTA conjugated QD nanoparticles and the successful application of these nanoparticles to the detection of histicline-tagged fusion proteins. It is believed that this approach will provide a more convenient methodology for the intracellular localization of histidine-tagged protein, as compared with current methods. These Ni-NTA-QD clusters were shown to target the 6x histidine region of tagged proteins specially. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:836 / 842
页数:7
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