Illuminating Insights into Firefly Luciferase and Other Bioluminescent Reporters Used in Chemical Biology

被引:238
作者
Thorne, Natasha [1 ]
Inglese, James [1 ]
Auldl, Douglas S. [1 ]
机构
[1] NIH, NIH Chem Genom Ctr, Bethesda, MD 20892 USA
来源
CHEMISTRY & BIOLOGY | 2010年 / 17卷 / 06期
关键词
GREEN FLUORESCENT PROTEIN; SMALL-MOLECULE ACTIVATORS; GAUSSIA LUCIFERASE; COENZYME-A; SECRETED LUCIFERASE; EXPRESSION; GENE; ASSAYS; IDENTIFICATION; LUMINESCENCE;
D O I
10.1016/j.chembiol.2010.05.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Understanding luciferase enzymology and the structure of compounds that modulate luciferase activity can be used to improve the design of luminescence-based assays. This review provides an overview of these popular reporters with an emphasis on the commonly used firefly luciferase from Photinus pyralis (FLuc). Large-scale chemical profile studies have identified a variety of scaffolds that inhibit FLuc. In some cell-based assays, these inhibitors can act in a counterintuitive way, leading to a gain in luminescent signal. Although formerly attributed to transcriptional activation, intracellular stabilization of FLuc is the primary mechanism underlying this observation. FLuc inhibition and stabilization can be complex, as illustrated by the compound PTC124, which is converted by FLuc in the presence of ATP to a high affinity multisubstrate adduct inhibitor, PTC124-AMP. The potential influence these findings can have on drug discovery efforts is provided here.
引用
收藏
页码:646 / 657
页数:12
相关论文
共 69 条
[1]
Almond B., 2003, Promega Notes, P11
[2]
A specific mechanism for nonspecific activation in reporter-gene assays [J].
Auld, Douglas S. ;
Thorne, Natasha ;
Nguyen, Dac-Trung ;
Inglese, James .
ACS CHEMICAL BIOLOGY, 2008, 3 (08) :463-470
[3]
Characterization of chemical libraries for luciferase inhibitory activity [J].
Auld, Douglas S. ;
Southall, Noel T. ;
Jadhav, Ajit ;
Johnson, Ronald L. ;
Diller, David J. ;
Simeonov, Anton ;
Austin, Christopher P. ;
Inglese, James .
JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (08) :2372-2386
[4]
Molecular basis for the high-affinity binding and stabilization of firefly luciferase by PTC124 [J].
Auld, Douglas S. ;
Lovell, Scott ;
Thorne, Natasha ;
Lea, Wendy A. ;
Maloney, David J. ;
Shen, Min ;
Rai, Ganesha ;
Battaile, Kevin P. ;
Thomas, Craig J. ;
Simeonov, Anton ;
Hanzlik, Robert P. ;
Inglese, James .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (11) :4878-4883
[5]
Mechanism of PTC124 activity in cell-based luciferase assays of nonsense codon suppression [J].
Auld, Douglas S. ;
Thorne, Natasha ;
Maguire, William F. ;
Inglese, James .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (09) :3585-3590
[6]
A Basis for Reduced Chemical Library Inhibition of Firefly Luciferase Obtained from Directed Evolution [J].
Auld, Douglas S. ;
Zhang, Ya-Qin ;
Southall, Noel T. ;
Rai, Ganesha ;
Landsman, Marc ;
MacLure, Jennifer ;
Langevin, Daniel ;
Thomas, Craig J. ;
Austin, Christopher P. ;
Inglese, James .
JOURNAL OF MEDICINAL CHEMISTRY, 2009, 52 (05) :1450-1458
[7]
Resveratrol inhibits firefly luciferase [J].
Bakhtiarova, Adel ;
Taslimi, Paul ;
Elliman, Stephen J. ;
Kosinski, Penelope A. ;
Hubbard, Brian ;
Kavana, Michael ;
Kemp, Daniel M. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 351 (02) :481-484
[8]
Firefly luciferase: The structure is known, but the mystery remains [J].
Baldwin, TO .
STRUCTURE, 1996, 4 (03) :223-228
[9]
Engineered luciferases for molecular sensing in living cells [J].
Binkowski, Brock ;
Fan, Frank ;
Wood, Keith .
CURRENT OPINION IN BIOTECHNOLOGY, 2009, 20 (01) :14-18
[10]
Luminogenic cytochrome P450 assays [J].
Cali, James J. ;
Ma, Dongping ;
Sobol, Mary ;
Simpson, Daniel J. ;
Frackman, Susan ;
Good, Troy I. ;
Daily, William J. ;
Liu, David .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2006, 2 (04) :629-645