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Single-Stranded DNA Assisted Cell Penetrating Peptide-DNA Conjugation Strategy for Intracellular Imaging of Nucleases

机译:单链DNA辅助细胞穿透肽-DNA结合策略的核酸酶细胞内成像。

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摘要

Cell penetrating peptides (CPPs) are very useful tools for delivery of DNA molecules into living cells without damaging the cell membranes. However, covalent conjugation of DNAs to CPPs is technically difficult, and the reactions between DNA and target nucleases are also liable to be affected by the cationic CPP molecules. In this work, we demonstrate that the electrostatic interactions between CPPs and single-stranded DNA (ssDNA) were stronger than those between CPP and double-stranded DNA (dsDNA). Taking advantage of this property, we developed an ssDNA protected CPP DNA fluorescent probe which allowed for noninvasive and efficient cellular uptake and rapid imaging of target nucleases in living cells. The probe is highly sensitive and selective. This work represents the first example of using CPP-DNA conjugate to deliver DNA fluorescent probes for in situ imaging of nucleases within cells. The developed approach also holds great potential for the cellular delivery of other nucleic acid molecules for diagnosis or therapeutics purposes.
机译:细胞穿透肽(CPPs)是非常有用的工具,用于将DNA分子递送到活细胞中而不会损坏细胞膜。然而,DNA与CPP的共价结合在技术上是困难的,并且DNA与靶核酸酶之间的反应也容易受到阳离子CPP分子的影响。在这项工作中,我们证明了CPP和单链DNA(ssDNA)之间的静电相互作用比CPP和双链DNA(dsDNA)之间的静电相互作用更强。利用这一特性,我们开发了一种受ssDNA保护的CPP DNA荧光探针,该探针可实现无创且有效的细胞摄取,并能快速成像活细胞中靶核酸酶。该探针是高度敏感和选择性的。这项工作代表了使用CPP-DNA偶联物递送DNA荧光探针进行细胞内核酸酶原位成像的第一个例子。所开发的方法还具有用于诊断或治疗目的的其他核酸分子的细胞递送的巨大潜力。

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