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分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

蛋白质组学研究试剂 蛋白定量提取试剂盒供应商 蛋白实验试剂厂家-翌圣生物

Bifunctional carbon dots for cell imaging and inhibition of human insulin fibrillation in the whole aggregation process

Bei-Bei Wang, Yu-Ying Wang, Xiao-Yang Zhang, Zi-Qiang Xu, Peng Jiang, Feng-Lei Jiang, Yi Liu

Journal:INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES

IF:5.16

DOI:10.1016/j.ijbiomac.2019.12.267

PMID:31923519

Published:2020-01-07

research field:细胞生物学干细胞生物学消化生物学代谢组学遗传学与基因组学发育生物学表观遗传学

Abstract

Due to the favorable stability, water solubility and good biocompatibility, carbon dots have attracted much attention. Herein, a novel nitrogen-doping bifunctional carbon dots (N-BCDs) with ultra-highly quantum yield ( QY abs  = 70.4%) is prepared through microwave-assisted method. 50 μg/mL of N-BCDs emit intense fluorescence in HeLa and GES-1 cells with negligible cytotoxicity. In addition, effective inhibition of N-BCDs to human insulin (HI) fibrillation is observed even at 10:1 (mass ratio of HI: N-BCDs) by ThT fluorescence, CD assay and TEM. N-BCDs prevent HI from fibrillation with prolonged lag time and reduced fluorescent intensity at equilibrium, regardless of the addition time of N-BCDs (HI: N-BCDs = 1:1, mass ratio), which has been rarely reported before. Furthermore, the morphology of final HI fibrils is shorter and thinner in the presence of N-BCDs. Mechanism studies reveal that the enhanced hydrogen bond between HI monomers and N-BCDs inhibits nucleation during the lag stage ( K a : 1.54 × 10 4  L·mol − 1 , 298 K), while the accumulation of N-BCDs blocks the growth of profibrils in the elongation stage. To the best of our knowledge, it's the first time to observe the accumulation of N-BCDs around HI profibrils with TEM. Our study provides a new strategy for developing efficient nanoparticle inhibitors for protein fibrillation.

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