Molecular beacons for detecting DNA binding proteins: mechanism of action

被引:34
作者
Heyduk, E [1 ]
Knoll, E [1 ]
Heyduk, T [1 ]
机构
[1] St Louis Univ, Sch Med, Edward A Doisy Dept Biochem & Mol Biol, St Louis, MO 63104 USA
关键词
DNA binding proteins; detection; fluorescence;
D O I
10.1016/S0003-2697(03)00004-6
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
New methodology for detecting sequence-specific DNA binding proteins has been recently developed (T. Heyduk, and E. Heyduk, Nat. Biotechnol. 20 (2002) 171). The central feature of this assay is protein-dependent association of two DNA fragments, each containing about half of a DNA sequence-defining the protein binding site. In this report we propose a physical model explaining the functioning of the assay. The model involves two linked equilibria: association between the two DNA fragments and binding of the protein exclusively to the complex between the two DNA fragments. Equilibrium and kinetic experiments provided evidence supporting the proposed model and showed that the model was sufficient to describe the behavior of the assay under a variety of conditions. Kinetic data identified the association between the two DNA half-sites as the rate-limiting step of the assay. Theoretical simulations based on the proposed model were used to investigate parameters important for the maximal sensitivity of the assay. Physical understanding of the assay will provide means for rational design of the assay for a variety of target proteins. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 15 条
[1]
Transcription - Signal transduction and the control of gene expression [J].
Brivanlou, AH ;
Darnell, JE .
SCIENCE, 2002, 295 (5556) :813-818
[2]
Transcription activation by catabolite activator protein (CAP) [J].
Busby, S ;
Ebright, RH .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 293 (02) :199-213
[3]
CONSENSUS DNA SITE FOR THE ESCHERICHIA-COLI CATABOLITE GENE ACTIVATOR PROTEIN (CAP) - CAP EXHIBITS A 450-FOLD HIGHER AFFINITY FOR THE CONSENSUS DNA SITE THAN FOR THE ESCHERICHIA-COLI LAC DNA SITE [J].
EBRIGHT, RH ;
EBRIGHT, YW ;
GUNASEKERA, A .
NUCLEIC ACIDS RESEARCH, 1989, 17 (24) :10295-10305
[4]
EQUILIBRIA AND KINETICS OF LAC REPRESSOR-OPERATOR INTERACTIONS BY POLYACRYLAMIDE-GEL ELECTROPHORESIS [J].
FRIED, M ;
CROTHERS, DM .
NUCLEIC ACIDS RESEARCH, 1981, 9 (23) :6505-6525
[5]
Thiol-reactive, luminescent europium chelates: Luminescence probes for resonance energy transfer distance measurements in biomolecules [J].
Heyduk, E ;
Heyduk, T .
ANALYTICAL BIOCHEMISTRY, 1997, 248 (02) :216-227
[6]
APPLICATION OF FLUORESCENCE ENERGY-TRANSFER AND POLARIZATION TO MONITOR ESCHERICHIA-COLI CAMP RECEPTOR PROTEIN AND LAC PROMOTER INTERACTION [J].
HEYDUK, T ;
LEE, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (05) :1744-1748
[7]
ESCHERICHIA-COLI CAMP RECEPTOR PROTEIN - EVIDENCE FOR 3 PROTEIN CONFORMATIONAL STATES WITH DIFFERENT PROMOTER BINDING AFFINITIES [J].
HEYDUK, T ;
LEE, JC .
BIOCHEMISTRY, 1989, 28 (17) :6914-6924
[8]
Molecular beacons for detecting DNA binding proteins [J].
Heyduk, T ;
Heyduk, E .
NATURE BIOTECHNOLOGY, 2002, 20 (02) :171-176
[9]
Lakowicz J.R., 2004, PRINCIPLES FLUORESCE, VSecond
[10]
Lewin B., 2000, Genes, VVII