Fluorescence Imaging of siRNA Delivery by Peptide Nucleic Acid-based Probe

被引:16
作者
Sato, Takaya [1 ]
Sato, Yusuke [1 ]
Iwai, Kenta [2 ]
Kuge, Shusuke [2 ]
Teramae, Norio [1 ]
Nishizawa, Seiichi [1 ]
机构
[1] Tohoku Univ, Grad Sch Sci, Dept Chem, Aoba Ku, Sendai, Miyagi 9808578, Japan
[2] Tohoku Pharmaceut Univ, Dept Microbiol, Aoba Ku, Sendai, Miyagi 9818558, Japan
关键词
Small interfering RNA (siRNA); RNA interference (RNAi); peptide nucleic acid; thiazole orange; fluorescence microscopy; siRNA delivery; delivery carrier; affinity-labeling; RNA INTERFERENCE; ENDOSOMAL ESCAPE; GENE DELIVERY; IN-VIVO; CELLS; THERAPEUTICS; FORMULATIONS; CANCER;
D O I
10.2116/analsci.31.315
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We report on the use of a peptide nucleic acid (PNA)-based fluorescent probe for the analysis of siRNA delivery to living cells. The probe, Py-AA-TO, possesses thiazole orange (TO) and pyrene moieties in the C- and N-termini of PNA, and can function as a light-up probe capable of selective binding to 3'-overhanging nucleotides of target siRNAs. The affinity-labeling of the siRNAs with Py-AA-TO facilitates fluorescence imaging of cellular uptake of polymer-based carriers encapsulating the siRNAs (polyplexes) through endocytosis and subsequent sequestration into lysosome. In addition, flow cytometric measurements reveal that the monitoring of Py-AA-TO fluorescence inside the cells is successfully applicable to the analysis of the polyplex disassembly. These promising functions of Py-AA-TO are presented and discussed as a basis for the design of molecular probes for fluorescent imaging and quantitative analysis of the siRNA delivery process.
引用
收藏
页码:315 / 320
页数:6
相关论文
共 32 条
[1]   Nanoparticles for ex vivo siRNA delivery to dendritic cells for cancer vaccines: Programmed endosomal escape and dissociation [J].
Akita, Hidetaka ;
Kogure, Kentaro ;
Moriguchi, Rumiko ;
Nakamura, Yoshio ;
Higashi, Tomoko ;
Nakamura, Takashi ;
Serada, Satoshi ;
Fujimoto, Minoru ;
Naka, Tetsuji ;
Futaki, Shiroh ;
Harashima, Hideyoshi .
JOURNAL OF CONTROLLED RELEASE, 2010, 143 (03) :311-317
[2]   FRET-Labeled siRNA Probes for Tracking Assembly and Disassembly of siRNA Nanocomplexes [J].
Alabi, Christopher A. ;
Love, Kevin T. ;
Sahay, Gaurav ;
Stutzman, Tina ;
Young, Whitney T. ;
Langer, Robert ;
Anderson, Daniel G. .
ACS NANO, 2012, 6 (07) :6133-6141
[3]   A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE [J].
BOUSSIF, O ;
LEZOUALCH, F ;
ZANTA, MA ;
MERGNY, MD ;
SCHERMAN, D ;
DEMENEIX, B ;
BEHR, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7297-7301
[4]   Gene delivery with tow molecular weight linear polyethytenimines [J].
Breunig, M ;
Lungwitz, U ;
Liebl, R ;
Fontanari, C ;
Klar, J ;
Kurtz, A ;
Blunk, T ;
Goepferich, A .
JOURNAL OF GENE MEDICINE, 2005, 7 (10) :1287-1298
[5]   Breaking up the correlation between efficacy and toxicity for nonviral gene delivery [J].
Breunig, Miriam ;
Lungwitz, Uta ;
Liebl, Renate ;
Goepferich, Achim .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (36) :14454-14459
[6]   RNA-Based Therapeutics: Current Progress and Future Prospects [J].
Burnett, John C. ;
Rossi, John J. .
CHEMISTRY & BIOLOGY, 2012, 19 (01) :60-71
[7]   Monitoring the disassembly of siRNA polyplexes in serum is crucial for predicting their biological efficacy [J].
Buyens, Kevin ;
Meyer, Martin ;
Wagner, Ernst ;
Demeester, Joseph ;
De Smedt, Stefaan C. ;
Sanders, Niek N. .
JOURNAL OF CONTROLLED RELEASE, 2010, 141 (01) :38-41
[8]   RNAi in human cells: Basic structural and functional features of small interfering RNA [J].
Chiu, YL ;
Rana, TM .
MOLECULAR CELL, 2002, 10 (03) :549-561
[9]   Evidence of RNAi in humans from systemically administered siRNA via targeted nanoparticles [J].
Davis, Mark E. ;
Zuckerman, Jonathan E. ;
Choi, Chung Hang J. ;
Seligson, David ;
Tolcher, Anthony ;
Alabi, Christopher A. ;
Yen, Yun ;
Heidel, Jeremy D. ;
Ribas, Antoni .
NATURE, 2010, 464 (7291) :1067-U140
[10]   Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells [J].
Elbashir, SM ;
Harborth, J ;
Lendeckel, W ;
Yalcin, A ;
Weber, K ;
Tuschl, T .
NATURE, 2001, 411 (6836) :494-498