Forster resonance energy transfer analysis of quantum dots and peptide self-assembly inside a capillary

被引:17
|
作者
Wang, Jianhao [1 ]
Qin, Yuqin [2 ]
Li, Jinchen [1 ]
Zhou, Xiang [3 ]
Yao, Yi [3 ]
Wang, Cheli [2 ]
Qiu, Lin [1 ]
Jiang, Pengju [1 ]
机构
[1] Changzhou Univ, Sch Pharmaceut Engn & Life Sci, Changzhou 213164, Jiangsu, Peoples R China
[2] Changzhou Univ, Sch Petrochem Engn, Changzhou 213164, Jiangsu, Peoples R China
[3] Changzhou Qianhong Biopharma Co Ltd, Changzhou 213164, Jiangsu, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
Quantum dots; CE-FL; In-capillary; Self-assembly; IN-VITRO SELECTION; LIVE CELLS; FRET; ELECTROPHORESIS; BIOSENSORS; AFFINITY; DONORS; INHIBITORS; SURFACE; DESIGN;
D O I
10.1016/j.snb.2015.12.086
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have developed a new method using fluorescence coupled capillary electrophoresis (CE-FL) for monitoring self-assembly of quantum dots (QDs) and ATTO 590 labeled peptide (ATTO-EA(5)H(6)) inside a capillary. QDs and ATTO-EA(5)H(6) were sequentially injected into the capillary, thereafter they mixed and self-assembled inside the capillary. Such in-capillary self-assembly was driven by a metal-affinity force which yielded a new fluorescence signal due to Forster resonance energy transfer (FRET). CE-FL was used to measure and record the self-assembly status and rate with electrophoretograms under various conditions. Recorded electrophoretograms have shown that in-capillary assay gave out different patterns of the assembly compared to out-capillary assay. The efficiency of the QDs and ATTO-EA(5)H(6) self-assembly on in-capillary assay was affected by the molar ratio and the time interval of injection. More importantly, the in-capillary assay could be applied to detect the stability of QD-ATTO-EA(5)H(6) assembly. The results indicated that high concentration of imidazole (Im) could displace a portion of ATTO-EA(5)H(6) on QDs surface. This assay could further expand the application of FRET in the field of QDs-based online bioanalysis. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:619 / 625
页数:7
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