NANOSTRUCTURED PROBES FOR IN VIVO GENE DETECTION.

Gang Bao, Phillip Santangelo, Nitin Nitin, Won Jong Rhee
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Abstract

The ability to visualize in real-time the expression dynamics and localization of specific RNAs in vivo offers tremendous opportunities for biological and disease studies including cancer detection. However, quantitative methods such as real-time PCR and DNA microarrays rely on the use of cell lysates thus not able to obtain important spatial and temporal information. Fluorescence proteins and other reporter systems cannot image endogenous RNA in living cells. Fluorescence in situ hybridization (FISH) assays require washing to achieve specificity, therefore can only be used with fixed cells. Here we review the recent development of nanostructured probes for living cell RNA detection, and discuss the biological and engineering issues and challenges of quantifying gene expression in vivo. In particular, we describe methods that use oligonucleotide probes, combined with novel delivery strategies, to image the relative level, localization and dynamics of RNA in live cells. Examples of detecting endogenous mRNAs, as well as imaging their subcellular localization are given to illustrate the biological applications, and issues in probe design, delivery and target accessibility are discussed. The nanostructured probes promise to open new and exciting opportunities in sensitive gene detection for a wide range of biological and medical applications.

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用于体内基因检测的纳米结构探针。
实时可视化体内特定rna的表达动态和定位的能力为包括癌症检测在内的生物学和疾病研究提供了巨大的机会。然而,定量方法,如实时PCR和DNA微阵列依赖于使用细胞裂解物,因此无法获得重要的空间和时间信息。荧光蛋白和其他报告系统不能成像活细胞中的内源性RNA。荧光原位杂交(FISH)检测需要洗涤才能达到特异性,因此只能用于固定细胞。本文综述了用于活细胞RNA检测的纳米探针的最新进展,并讨论了定量基因在体内表达的生物学和工程问题和挑战。特别是,我们描述了使用寡核苷酸探针的方法,结合新的递送策略,来成像活细胞中RNA的相对水平,定位和动态。本文给出了检测内源性mrna及其亚细胞定位成像的例子,以说明其生物学应用,并讨论了探针设计、递送和靶标可及性等问题。纳米结构探针有望在敏感基因检测方面开辟新的和令人兴奋的机会,用于广泛的生物和医学应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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