Molecular Beacon Nano-Sensors for Probing Living Cancer Cells

分子信标 细胞内 癌变 癌细胞 生物传感器 细胞质 生物 计算生物学 癌症 DNA 细胞生物学 化学 纳米技术 分子生物学 生物化学 遗传学 材料科学 寡核苷酸
作者
Tairong Kuang,Lingqian Chang,Xiangfang Peng,Xianglong Hu,Daniel Gallego‐Perez
出处
期刊:Trends in Biotechnology [Elsevier]
卷期号:35 (4): 347-359 被引量:62
标识
DOI:10.1016/j.tibtech.2016.09.003
摘要

Precisely controlling the dose of MBs delivered into live cells, which allows quantitative analysis at single-cell resolution, is becoming increasingly feasible. The design of MBs is moving towards increased sensitivity and longer-lasting resistance to nucleases and other enzymes. The 'specificity' parameter is particularly important for prognostic bio-chips and in vivo imaging. MB designs that address single-nucleotide mutations and that can detect multiple targets are becoming popular. Heterogeneities and oncogenesis essentially result from proteomic disorders orchestrated by changes in DNA and/or cytoplasmic mRNA. These genetic fluctuations, however, cannot be decoded through conventional label-free methods (e.g., patch clamps, electrochemical cellular biosensors, etc.) or morphological characterization. Molecular beacons (MBs) have recently emerged as efficient probes for interrogating biomarkers in live cancer cells. MBs hybridize with their intracellular targets (e.g., mRNAs, DNAs, or proteins), emitting a fluorescent signal that can be quantified and correlated with the expression levels of their targets. In this review we discuss MB probes with different delivery platforms for intracellular probing as well as novel MB designs for detecting a variety of targets in living cancer cells. Finally, we describe current trends in MB-based intracellular biosensors. Heterogeneities and oncogenesis essentially result from proteomic disorders orchestrated by changes in DNA and/or cytoplasmic mRNA. These genetic fluctuations, however, cannot be decoded through conventional label-free methods (e.g., patch clamps, electrochemical cellular biosensors, etc.) or morphological characterization. Molecular beacons (MBs) have recently emerged as efficient probes for interrogating biomarkers in live cancer cells. MBs hybridize with their intracellular targets (e.g., mRNAs, DNAs, or proteins), emitting a fluorescent signal that can be quantified and correlated with the expression levels of their targets. In this review we discuss MB probes with different delivery platforms for intracellular probing as well as novel MB designs for detecting a variety of targets in living cancer cells. Finally, we describe current trends in MB-based intracellular biosensors.
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