Wang Jianhao, Li Jingyan, Chen Yao, Teng Yiwan, Wang Cheli, Li Jinchen, Liu Li, Dong Bingyu, Qiu Lin, Jiang Pengju
School of Pharmaceutical Engineering and Life Science, Changzhou University, Changzhou, Jiangsu, P. R. China.
Electrophoresis. 2015 Oct;36(19):2419-24. doi: 10.1002/elps.201500205. Epub 2015 Aug 18.
Herein, we designed four peptides appended with different numbers of histidine (Hisn -peptide). We launched a systematic investigation on quantum dots (QDs) and Hisn -peptide self-assembly in solution using fluorescence coupled CE (CE-FL). The results indicated that CE-FL was a powerful method to probe how ligands interaction on the surface of nanoparticles. The self-assembly of QDs and peptide was determined by the numbers of histidine. We also observed that longer polyhistidine tags (n ≤ 6) could improve the self-assembly efficiency. Furthermore, the formation and separation of QD-peptide assembly were also studied by CE-FL inside a capillary. The total time for the mixing, self-assembly, separation, and detection was less than 10 min. Our method greatly expands the application of CE-FL in QDs-based biolabeling and bioanalysis.
在此,我们设计了四种连接有不同数量组氨酸的肽(Hisn-肽)。我们使用荧光耦合毛细管电泳(CE-FL)对溶液中的量子点(QD)和Hisn-肽自组装进行了系统研究。结果表明,CE-FL是一种探测纳米颗粒表面配体相互作用的有力方法。量子点和肽的自组装由组氨酸的数量决定。我们还观察到较长的聚组氨酸标签(n≤6)可以提高自组装效率。此外,还通过毛细管内的CE-FL研究了量子点-肽组装体的形成和分离。混合、自组装、分离和检测的总时间不到10分钟。我们的方法极大地扩展了CE-FL在基于量子点的生物标记和生物分析中的应用。