Near-Infrared-Responded High Sensitivity Nanoprobe for Steady and Visualized Detection of Albumin in Hepatic Organoids and Mouse Liver.
Guofeng LiuJinsong WeiXiaoyu LiMeng TianZhenxing WangCongcong ShenWan SunChonghui LiXuewen LiEnguang LvShizheng TianJihua WangShicai XuBing ZhaoPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2022)
Exploring the advanced techniques for protein detection facilitates cell fate investigation. However, it remains challenging to quantify and visualize the protein with one single probe. Here, a luminescent approach to detect hepatic cell fate marker albumin in vitro and living cell labeling with upconversion nanoparticles (UCNPs), which are conjugated with antibody (Ab) and rose bengal hexanoic acid (RBHA) is reported. To guarantee the detection quality and accuracy, an "OFF-ON" strategy is adopted: in the presence of albumin, the luminescence of nanoparticles remains suppressed owing to energy transfer to the quencher. Upon albumin binding to the antibody, the luminescence is recovered under near-infrared light. In various bio-samples, the UCNPs-Ab-RBHA (UCAR) nanoprobe can sense albumin with a broad detection range (5-315 ng mL -1 ). When applied to liver ductal organoid culture medium, the UCAR can monitor hepatocyte differentiation in real time by sensing the secreted albumin. Further, UCAR enables live imaging of cellular albumin in cells, organoids, and tissues. In a CCl 4 -induced liver injury model, UCAR detects reduced albumin in liver tissue and serum. Thus, a biocompatible nanoprobe for both quantification and imaging of protein in complex biological environment with superior stability and high sensitivity is provided.
Keyphrases
- energy transfer
- cell fate
- quantum dots
- loop mediated isothermal amplification
- real time pcr
- living cells
- high resolution
- label free
- photodynamic therapy
- gene expression
- amino acid
- binding protein
- single cell
- mass spectrometry
- stem cells
- liver injury
- oxidative stress
- mesenchymal stem cells
- bone marrow
- small molecule
- drug induced
- cell therapy
- fluorescence imaging