Multi-Path Quenchers: Efficient Quenching of Common Fluorophores

被引:53
作者
Crisalli, Pete [1 ]
Kool, Eric T. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
RESONANCE ENERGY-TRANSFER; MOLECULAR BEACONS; FLUORESCENCE; PROBES; ACENAPHTHENE; DERIVATIVES; DYE;
D O I
10.1021/bc200424r
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Fluorescence quenching groups are widely employed in biological detection, sensing, and imaging. To date, a relatively small number of such groups are in common use. Perhaps the most commonly used quencher, dabcyl, has limited efficiency with a broad range of fluorophores. Here, we describe a molecular approach to improve the efficiency of quenchers by increasing their electronic complexity. Multi-Path Quenchers (MPQ) are designed to have multiple donor or acceptor groups in their structure, allowing for a multiplicity of conjugation pathways of varied length. This has the effect of broadening the absorption spectrum, which in turn can increase quenching efficiency and versatility. Six such MPQ derivatives are synthesized and tested for quenching efficiency in a DNA hybridization context. Duplexes placing quenchers and fluorophores within contact distance or beyond this distance are used to measure quenching via contact or FRET mechanisms. Results show that several of the quenchers are considerably more efficient than dabcyl at quenching a wider range of. common fluorophores, and two quench fluorescein and TAMRA as well as or better than a Black Hole Quencher.
引用
收藏
页码:2345 / 2354
页数:10
相关论文
共 35 条
[1]
NEAR-INFRARED-ABSORBING SQUARAINE DYES CONTAINING 2,3-DIHYDROPERIMIDINE TERMINAL GROUPS [J].
BELLO, KA ;
CORNS, SN ;
GRIFFITHS, J .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1993, (05) :452-454
[2]
Bernacchi S, 2001, Nucleic Acids Res, V29, pE62, DOI 10.1093/nar/29.13.e62
[3]
Dynamic imaging of protease activity with fluorescently quenched activity-based probes [J].
Blum, G ;
Mullins, SR ;
Keren, K ;
Fonovic, M ;
Jedeszko, C ;
Rice, MJ ;
Sloane, BF ;
Bogyo, M .
NATURE CHEMICAL BIOLOGY, 2005, 1 (04) :203-209
[4]
PLEIADENE SYSTEMS .2. ON MECHANISM OF ACEPLEIADYLENE FORMATION - A VINYLOGOUS ELEIMINATION IN ACENAPHTHENE SERIES [J].
CAVA, MP ;
MERKEL, KE ;
SCHLESSI.RH .
TETRAHEDRON, 1965, 21 (11) :3059-&
[5]
Cook R. M., 2006, U.S. Patent, Patent No. [7,019,129, 7019129]
[6]
Protease Probes Built from DNA: Multispectral Fluorescent DNA-Peptide Conjugates as Caspase Chemosensors [J].
Dai, Nan ;
Guo, Jia ;
Teo, Yin Nah ;
Kool, Eric T. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (22) :5105-5109
[7]
DNA-polyfluorophore excimers as sensitive reporters for esterases and lipases [J].
Dai, Nan ;
Teo, Yin Nah ;
Kool, Eric T. .
CHEMICAL COMMUNICATIONS, 2010, 46 (08) :1221-1223
[8]
Two Successive Reactions on a DNA Template: A Strategy for Improving Background Fluorescence and Specificity in Nucleic Acid Detection [J].
Franzini, Raphael M. ;
Kool, Erie T. .
CHEMISTRY-A EUROPEAN JOURNAL, 2011, 17 (07) :2168-2175
[9]
Efficient Nucleic Acid Detection by Templated Reductive Quencher Release [J].
Franzini, Raphael M. ;
Kool, Eric T. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (44) :16021-+
[10]
Synthesis and characterization of novel monoazo N-ester-1,8-naphthalimide disperse dyestuffs [J].
Gharanjig, Kamaladin ;
Arami, Mokhtar ;
Rouhani, Shohre ;
Bahrami, Hajir ;
Movassagh, Barahman ;
Mahmoodi, Niyaz Mohammad .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 2007, 54 (04) :1021-1028