研究目的
Developing a novel amplified split aptamer sensor for highly sensitive detection and imaging of small molecules in living cells.
研究成果
The amplified split aptamer sensor provides a highly sensitive and selective method for ATP detection and imaging in living cells, with potential applications in detecting low-abundance biomarkers.
研究不足
The study focuses on ATP as the model target; applicability to other small molecules needs further investigation. The delivery efficiency and specificity in different cell types are not extensively explored.
1:Experimental Design and Method Selection:
The study combines two split aptamer fragments with HCR amplification to minimize background and improve signal-to-background ratio. Cationic BCNs with entrapped fluorescent conjugated polymer are used as a delivery agent.
2:Sample Selection and Data Sources:
HeLa cells are used for live cell studies.
3:List of Experimental Equipment and Materials:
Includes block copolymer nanoparticles, fluorescent conjugated polymer, DNA probes (AP1, AP2, H1, H2), and ATP as the model target.
4:Experimental Procedures and Operational Workflow:
The BCNs-DNA nanocomplex is formed and delivered into cells. The activation of fluorescence signal is specific to ATP-mediated assembly of two split aptamer fragments.
5:Data Analysis Methods:
Fluorescence spectral responses and gel electrophoresis analysis are used to validate the design.
独家科研数据包,助您复现前沿成果,加速创新突破
获取完整内容