通过 PNA-DNA 链置换激活探针成像活细胞中的 mRNA 表达。

IF 1.3 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Journal of Nucleic Acids Pub Date : 2012-01-01 Epub Date: 2012-09-26 DOI:10.1155/2012/962652
Zhenghui Wang, Ke Zhang, Karen L Wooley, John-Stephen Taylor
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引用次数: 0

摘要

用于监测体内 mRNA 表达的探针对研究生物和生物医学问题具有重大意义,但由于信噪比差和无法有效地将探针送入活细胞,研究进展一直受阻。在此,我们报告了一种 PNA-DNA 链位移激活的荧光探针,它能对炎症标志物 iNOS(诱导型一氧化氮合酶)mRNA 的表达进行成像。该探针由荧光素标记的反义 PNA 与较短的 DABCYL(加)标记 DNA 退火组成,后者可淬灭荧光,但当淬灭链被目标 mRNA 取代时,荧光又会恢复。使用 DNA 作为淬灭链是为了促进原本为净醛的 PNA 链与阳离子壳交联的类克奈德(cSCK)纳米粒子的静电结合,与其他转染剂相比,这种纳米粒子能以更低的毒性和更高的效率将 PNA-DNA 双工探针送入细胞。通过 cSCK 转染了 iNOS PNA-DNA 探针的 RAW 264.7 小鼠巨噬细胞在受到 iNOS 刺激时,每个细胞的平均荧光增加了 16 到 54 倍。这一增幅是非互补探针的 4 到 7 倍,从而验证了 PNA-DNA 链位移激活探针对体内 mRNA 表达成像的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Imaging mRNA Expression in Live Cells via PNA·DNA Strand Displacement-Activated Probes.

Imaging mRNA Expression in Live Cells via PNA·DNA Strand Displacement-Activated Probes.

Imaging mRNA Expression in Live Cells via PNA·DNA Strand Displacement-Activated Probes.

Imaging mRNA Expression in Live Cells via PNA·DNA Strand Displacement-Activated Probes.

Probes for monitoring mRNA expression in vivo are of great interest for the study of biological and biomedical problems, but progress has been hampered by poor signal to noise and effective means for delivering the probes into live cells. Herein we report a PNA·DNA strand displacement-activated fluorescent probe that can image the expression of iNOS (inducible nitric oxide synthase) mRNA, a marker of inflammation. The probe consists of a fluorescein labeled antisense PNA annealed to a shorter DABCYL(plus)-labeled DNA which quenches the fluorescence, but when the quencher strand is displaced by the target mRNA the fluorescence is restored. DNA was used for the quencher strand to facilitate electrostatic binding of the otherwise netural PNA strand to a cationic shell crosslinked knedel-like (cSCK) nanoparticle which can deliver the PNA·DNA duplex probe into cells with less toxicity and greater efficiency than other transfection agents. RAW 264.7 mouse macrophage cells transfected with the iNOS PNA·DNA probe via the cSCK showed a 16 to 54-fold increase in average fluorescence per cell upon iNOS stimulation. The increase was 4 to 7-fold higher than that for a non-complementary probe, thereby validating the ability of a PNA·DNA strand displacement-activated probe to image mRNA expression in vivo.

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来源期刊
Journal of Nucleic Acids
Journal of Nucleic Acids BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
3.10
自引率
21.70%
发文量
5
审稿时长
12 weeks
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