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

Author:

Wang Zhenghui1,Zhang Ke1,Wooley Karen L.12,Taylor John-Stephen1

Affiliation:

1. Department of Chemistry, Washington University, St. Louis, MO 63130, USA

2. Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, TX 77842-3012, USA

Abstract

Probes for monitoring mRNA expressionin vivoare 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 shorterDABCYLplus-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 expressionin vivo.

Funder

National Heart, Lung, and Blood Institute

Publisher

Hindawi Limited

Subject

Molecular Biology,Biochemistry

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