共 35 条
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.
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页码:836 / 842
页数:7
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