Triplex-Forming Peptide Nucleic Acid Probe Having Thiazole Orange as a Base Surrogate for Fluorescence Sensing of Double-stranded RNA

被引:81
作者
Sato, Takaya [1 ]
Sato, Yusuke [1 ]
Nishizawa, Seiichi [1 ]
机构
[1] Tohoku Univ, Grad Sch Sci, Dept Chem, Sendai, Miyagi 9808578, Japan
关键词
PHYSIOLOGICALLY RELEVANT CONDITIONS; NUCLEOBASE-MODIFIED PNA; HELICAL RECOGNITION; DNA STAINS; FIT-PROBES; OLIGONUCLEOTIDES; DUPLEX; PH; HYBRIDIZATION; SEQUENCE;
D O I
10.1021/jacs.6b05554
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed a new fluorescent sensing probe for double-stranded RNA (dsRNA) by integrating thiazole orange (TO) as a base surrogate into triplex-forming PNA. Our probe forms the thermally stable triplex with the target dsRNA at acidic pH; and the triplex formation is accompanied by the remarkable light-up response of the TO unit. The binding of our probe to the target dsRNA proceeds very rapidly, allowing real-time monitoring of the triplex formation. Importantly, we found the TO base surrogate in our probe functions as a universal base for the base pair opposite the TO unit in the triplex formation. Furthermore, the TO unit is significantly more responsive for the fully matched dsRNA sequence compared to the mismatch-containing sequences, which enables the analysis of the target dsRNA sequence at the single-base pair resolution. The binding and sensing functions of our probe are described for the development of fluorescent probes applicable to sensing biologically relevant dsRNA.
引用
收藏
页码:9397 / 9400
页数:4
相关论文
共 31 条
[1]   A simple ligand that selectively targets CUG trinucleotide repeats and inhibits MBNL protein binding [J].
Arambula, Jonathan F. ;
Ramisetty, Sreenivasa Rao ;
Baranger, Anne M. ;
Zimmerman, Steven C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (38) :16068-16073
[2]   Structural diversity of target-specific homopyrimidine peptide nucleic acid-dsDNA complexes [J].
Bentin, Thomas ;
Hansen, Georg I. ;
Nielsen, Peter E. .
NUCLEIC ACIDS RESEARCH, 2006, 34 (20) :5790-5799
[3]   RNA triplexes: from structural principles to biological and biotech applications [J].
Devi, Gitali ;
Zhou, Yuan ;
Zhong, Zhensheng ;
Toh, Desiree-Faye Kaixin ;
Chen, Gang .
WILEY INTERDISCIPLINARY REVIEWS-RNA, 2015, 6 (01) :111-128
[4]   Incorporation of thio-pseudoisocytosine into triplex-forming peptide nucleic acids for enhanced recognition of RNA duplexes [J].
Devi, Gitali ;
Yuan, Zhen ;
Lu, Yunpeng ;
Zhao, Yanli ;
Chen, Gang .
NUCLEIC ACIDS RESEARCH, 2014, 42 (06) :4008-4018
[5]   AZOLE SUBSTITUTED OLIGONUCLEOTIDES PROMOTE ANTIPARALLEL TRIPLEX FORMATION AT NON-HOMOPURINE DUPLEX TARGETS [J].
DURLAND, RH ;
RAO, TS ;
BODEPUDI, V ;
SETH, DM ;
JAYARAMAN, K ;
REVANKAR, GR .
NUCLEIC ACIDS RESEARCH, 1995, 23 (04) :647-653
[6]   Nucleobase-Modified PNA Suppresses Translation by Forming a Triple Helix with a Hairpin Structure in mRNA InVitro and in Cells [J].
Endoh, Tamaki ;
Hnedzko, Dziyana ;
Rozners, Eriks ;
Sugimoto, Naoki .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (03) :899-903
[7]  
Grimm GN, 2002, CHEMBIOCHEM, V3, P324, DOI 10.1002/1439-7633(20020402)3:4<324::AID-CBIC324>3.0.CO
[8]  
2-7
[9]   Triple helical recognition of pyrimidine inversions in polypurine tracts of RNA by nucleobase-modified PNA [J].
Gupta, Pankaj ;
Zengeya, Thomas ;
Rozners, Eriks .
CHEMICAL COMMUNICATIONS, 2011, 47 (39) :11125-11127
[10]   Brightness Enhanced DNA FIT-Probes for Wash-Free RNA Imaging in Tissue [J].
Hoevelmann, Felix ;
Gaspar, Imre ;
Ephrussi, Anne ;
Seitz, Oliver .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (50) :19025-19032