Firefly Luciferase and Rluc8 Exhibit Differential Sensitivity to Oxidative Stress in Apoptotic Cells

被引:19
作者
Czupryna, Julie [1 ]
Tsourkas, Andrew [1 ]
机构
[1] Univ Penn, Dept Bioengn, Sch Engn & Appl Sci, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
CASPASE-INDEPENDENT MECHANISM; HYDROGEN-PEROXIDE; PROTEASOME INHIBITOR; LEUKEMIA-CELLS; CANCER CELLS; AMINO-ACIDS; PROTEIN; DEATH; DEGRADATION; ACTIVATION;
D O I
10.1371/journal.pone.0020073
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Over the past decade, firefly Luciferase (fLuc) has been used in a wide range of biological assays, providing insight into gene regulation, protein-protein interactions, cell proliferation, and cell migration. However, it has also been well established that fLuc activity can be highly sensitive to its surrounding environment. In this study, we found that when various cancer cell lines (HeLa, MCF-7, and 293T) stably expressing fLuc were treated with staurosporine (STS), there was a rapid loss in bioluminescence. In contrast, a stable variant of Renilla luciferase (RLuc), RLuc8, exhibited significantly prolonged functionality under the same conditions. To identify the specific underlying mechanism(s) responsible for the disparate sensitivity of RLuc8 and fLuc to cellular stress, we conducted a series of inhibition studies that targeted known intracellular protein degradation/modification pathways associated with cell death. Interestingly, these studies suggested that reactive oxygen species, particularly hydrogen peroxide (H(2)O(2)), was responsible for the diminution of fLuc activity. Consistent with these findings, the direct application of H(2)O(2) to HeLa cells also led to a reduction in fLuc bioluminescence, while H(2)O(2) scavengers stabilized fLuc activity. Comparatively, RLuc8 was far less sensitive to ROS. These observations suggest that fLuc activity can be substantially altered in studies where ROS levels become elevated and can potentially lead to ambiguous or misleading findings.
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页数:12
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共 44 条
[1]
Effects of proteasome inhibitor, MG132, on proteasorne activity and oxidative status of rat liver [J].
Alexandrova, Alberta ;
Petrov, Lubomir ;
Georgieva, Almira ;
Kirkova, Margarita ;
Kukan, Marian .
CELL BIOCHEMISTRY AND FUNCTION, 2008, 26 (03) :392-398
[2]
THE SULFHYDRYLS OF FIREFLY LUCIFERASE ARE NOT ESSENTIAL FOR ACTIVITY [J].
ALTER, SC ;
DELUCA, M .
BIOCHEMISTRY, 1986, 25 (07) :1599-1605
[3]
Thermostability of Firefly Luciferases Affects Efficiency of Detection by In Vivo Bioluminescence [J].
Baggett, Brenda ;
Roy, Rupali ;
Momen, Shafinaz ;
Morgan, Sherif ;
Tisi, Laurence ;
Morse, David ;
Gillies, Robert J. .
MOLECULAR IMAGING, 2004, 3 (04) :324-332
[4]
Complement-mediated cell death induced by rituximab in B-cell lymphoproliferative disorders is mediated in vitro by a caspase-independent mechanism involving the generation of reactive oxygen species [J].
Bellosillo, B ;
Villamor, N ;
López-Guillermo, A ;
Marcé, S ;
Esteve, J ;
Campo, E ;
Colomer, D ;
Montserrat, E .
BLOOD, 2001, 98 (09) :2771-2777
[5]
Protein oxidation in aging, disease, and oxidative stress [J].
Berlett, BS ;
Stadtman, ER .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (33) :20313-20316
[6]
Identification of a firefly luciferase active site peptide using a benzophenone-based photooxidation reagent [J].
Branchini, BR ;
Magyar, RA ;
Marcantonio, KM ;
Newberry, KJ ;
Stroh, JG ;
Hinz, LK ;
Murtiashaw, MH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (31) :19359-19364
[7]
Inactivation of firefly luciferase with N-(iodoacetyl)-N'-(5-sulfo-1-naphthyl)ethylenediamine (I-AEDANS) [J].
Branchini, BR ;
Magyar, RA ;
Murtiashaw, MH ;
Magnasco, N ;
Hinz, LK ;
Stroh, JG .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 340 (01) :52-58
[8]
Structural basis for the activation of phenylalanine in the non-ribosomal biosynthesis of gramicidin S [J].
Conti, E ;
Stachelhaus, T ;
Marahiel, MA ;
Brick, P .
EMBO JOURNAL, 1997, 16 (14) :4174-4183
[9]
UBIQUITIN PATHWAY INVOLVEMENT IN HUMAN LYMPHOCYTE GAMMA-IRRADIATION-INDUCED APOPTOSIS [J].
DELIC, J ;
MORANGE, M ;
MAGDELENAT, H .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (08) :4875-4883
[10]
FRANKE JC, BIOCH PHARM, V79, P575