Biochemical and cell biological assays to identify and characterize DNA helicase inhibitors

被引:20
作者
Banerjee, Taraswi [1 ]
Aggarwal, Monika [2 ]
Sommers, Joshua A. [1 ]
Brosh, Robert M., Jr. [1 ]
机构
[1] NIA, Lab Mol Gerontol, NIH, NIH Biomed Res Ctr, 251 Bayview Blvd, Baltimore, MD 21224 USA
[2] Georgetown Univ, Lombardi Comprehens Canc Res Ctr, Med Ctr, Washington, DC 20057 USA
关键词
Helicase; Replication; DNA repair; Small molecule; Inhibitor; Werner syndrome; Cancer therapy; WERNER-SYNDROME HELICASE; FANCONI-ANEMIA PATHWAY; HOMOLOGOUS RECOMBINATION; SYNTHETIC LETHALITY; RECENT PROGRESS; CANCER-THERAPY; REPAIR; TELOMERES; BINDING; DISSOCIATION;
D O I
10.1016/j.ymeth.2016.04.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The growing number of DNA helicases implicated in hereditary disorders and cancer indicates that this particular class of enzymes plays key roles in genomic stability and cellular homeostasis. Indeed, a large body of work has provided molecular and cellular evidence that helicases act upon a variety of nucleic acid substrates and interact with numerous proteins to enact their functions in replication, DNA repair, recombination, and transcription. Understanding how helicases operate in unique and overlapping pathways is a great challenge to researchers. In this review, we describe a series of experimental approaches and methodologies to identify and characterize DNA helicase inhibitors which collectively provide an alternative and useful strategy to explore their biological significance in cell-based systems. These procedures were used in the discovery of biologically active compounds that inhibited the DNA unwinding function catalyzed by the human WRN helicase-nuclease defective in the premature aging disorder Werner syndrome. We describe in vitro and in vivo experimental approaches to characterize helicase inhibitors with WRN as the model, anticipating that these approaches may be extrapolated to other DNA helicases, particularly those implicated in DNA repair and/or the replication stress response. Published by Elsevier Inc.
引用
收藏
页码:130 / 141
页数:12
相关论文
共 39 条
[1]   Characterization of the ATPase Activity of RecG and RuvAB Proteins on Model Fork Structures Reveals Insight into Stalled DNA Replication Fork Repair [J].
Abd Wahab, Syafiq ;
Choi, Meerim ;
Bianco, Piero R. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (37) :26397-26409
[2]   Targeting an Achilles' heel of cancer with a WRN helicase inhibitor [J].
Aggarwal, Monika ;
Banerjee, Taraswi ;
Sommers, Joshua A. ;
Brosh, Robert M., Jr. .
CELL CYCLE, 2013, 12 (20) :3329-3335
[3]   Werner Syndrome Helicase Has a Critical Role in DNA Damage Responses in the Absence of a Functional Fanconi Anemia Pathway [J].
Aggarwal, Monika ;
Banerjee, Taraswi ;
Sommers, Joshua A. ;
Iannascoli, Chiara ;
Pichierri, Pietro ;
Shoemaker, Robert H. ;
Brosh, Robert M., Jr. .
CANCER RESEARCH, 2013, 73 (17) :5497-5507
[4]   Inhibition of helicase activity by a small molecule impairs Werner syndrome helicase (WRN) function in the cellular response to DNA damage or replication stress [J].
Aggarwal, Monika ;
Sommers, Joshua A. ;
Shoemaker, Robert H. ;
Brosh, Robert M., Jr. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (04) :1525-1530
[5]   Hitting the Bull's Eye: Novel Directed Cancer Therapy Through Helicase-Targeted Synthetic Lethality [J].
Aggarwal, Monika ;
Brosh, Robert M., Jr. .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2009, 106 (05) :758-763
[6]   Identification of novel small-molecule compounds that inhibit the proproliferative Kruppel-like factor 5 in colorectal cancer cells by high-throughput screening [J].
Bialkowska, Agnieszka B. ;
Du, Yuhong ;
Fu, Haian ;
Yang, Vincent W. .
MOLECULAR CANCER THERAPEUTICS, 2009, 8 (03) :563-570
[7]   Thiazole orange as the fluorescent intercalator in a high resolution FID assay for determining DNA binding affinity and sequence selectivity of small molecules [J].
Boger, DL ;
Tse, WC .
BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (09) :2511-2518
[8]   Biochemical characterization of the DNA substrate specificity of Werner syndrome helicase [J].
Brosh, RM ;
Waheed, J ;
Sommers, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (26) :23236-23245
[9]   Enzymatic mechanism of the WRN helicase/nuclease [J].
Brosh, Robert M., Jr. ;
Opresko, Patricia L. ;
Bohr, Vilhelm A. .
DNA REPAIR, PT B, 2006, 409 :52-+
[10]   DNA helicases involved in DNA repair and their roles in cancer [J].
Brosh, Robert M., Jr. .
NATURE REVIEWS CANCER, 2013, 13 (08) :542-558