Lei Wang, Tingting Zhao, Congkai Wang, Xiaohan Xu, Wang Yao, Xiaozhe Pang, Shenghao Xu* and Xiliang Luo*,
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引用次数: 0
摘要
开发肿瘤细胞特异性成像方法对于清晰划分肿瘤边缘至关重要。然而,传统的成像方法存在反应动力学低、"始终处于活动状态 "的传感模式导致肿瘤特异性有限等问题,难以准确描绘肿瘤边界。针对这些局限性,我们开发了一种内源酶激活的空间限制 DNA 纳米线探针(E-SCNW),它具有更高的肿瘤/正常细胞分辨率,可用于肿瘤/正常细胞边界的高精度成像。空间限制效应可改善反应动力学,内源酶激活设计可将荧光反应限制在肿瘤细胞区域。此外,在穿过细胞膜进入细胞内空间时不需要额外的细胞输送载体。值得注意的是,得益于空间限制效应和内源酶活化设计,E-SCNW 的检测限降低了近 25.6 倍,肿瘤/正常细胞分辨比提高了近 4.46 倍,在肿瘤/正常细胞边界的高精度成像方面前景广阔。
Endogenous Enzyme-Activated Spatial Confinement DNA Nanowire with a Tumor Cell-Specific Response for High-Precision Imaging of the Tumor/Normal Cells Boundary
Developing tumor cell-specific imaging approaches is essential for the clear delineation of tumor margins. However, traditional imaging approaches suffered from low reaction kinetics as well as limited tumor specificity resulting from their “always active” sensing mode, making it difficult to accurately depict tumor boundary. To address these limitations, we developed an endogenous enzyme-activated spatial confinement DNA nanowire probe (E-SCNW) with an enhanced tumor/normal cell discrimination ratio for high precision imaging of the tumor/normal cells boundary. The spatial confinement effect can improve reaction kinetics, and the endogenous enzyme-activation design can confine fluorescence response to the tumor cells region. Additionally, no additional cell delivery carriers were required during the cross of the cell membrane into the intracellular space. It is worth noting that benefiting from the spatial confinement effect and endogenous enzyme-activation design, the detection limit was decreased by nearly 25.6-fold and the tumor/normal cells discrimination ratio was enhanced by nearly 4.46-fold through using E-SCNW, indicating promising prospects in high-precision imaging of the tumor/normal cells boundary.
期刊介绍:
Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.