TY - JOUR
T1 - Luminescent detection of DNA-binding proteins
AU - Leung, Chung Hang
AU - Chan, Daniel Shiu Hin
AU - He, Hong Zhang
AU - Cheng, Zhen
AU - Yang, Hui
AU - Ma, Dik Lung
N1 - Funding Information:
Funding for open access charge: Hong Kong Baptist University (FRG2/10-11/008); Environment and Conservation Fund (ECF Project 3/2010).
PY - 2012/2
Y1 - 2012/2
N2 - Transcription factors play a central role in cell development, differentiation and growth in biological systems due to their ability to regulate gene expression by binding to specific DNA sequences within the nucleus. The dysregulation of transcription factor signaling has been implicated in the pathogenesis of a number of cancers, developmental disorders, inflammation and autoimmunity. There is thus a high demand for convenient high-throughput methodologies able to detect sequence-specific DNA-binding proteins and monitor their DNA-binding activities. Traditional approaches for protein detection include gel mobility shift assays, DNA footprinting and enzyme-linked immunosorbent assays (ELISAs) which tend to be tedious, time-consuming, and may necessitate the use of radiographic labeling. By contrast, luminescence technologies offer the potential for rapid, sensitive and low-cost detection that are amenable to high-throughput and real-time analysis. The discoveries of molecular beacons and aptamers have spearheaded the development of new luminescent methodologies for the detection of proteins over the last decade. We survey here recent advances in the development of luminescent detection methods for DNA-binding proteins, including those based on molecular beacons, aptamer beacons, label-free techniques and exonuclease protection.
AB - Transcription factors play a central role in cell development, differentiation and growth in biological systems due to their ability to regulate gene expression by binding to specific DNA sequences within the nucleus. The dysregulation of transcription factor signaling has been implicated in the pathogenesis of a number of cancers, developmental disorders, inflammation and autoimmunity. There is thus a high demand for convenient high-throughput methodologies able to detect sequence-specific DNA-binding proteins and monitor their DNA-binding activities. Traditional approaches for protein detection include gel mobility shift assays, DNA footprinting and enzyme-linked immunosorbent assays (ELISAs) which tend to be tedious, time-consuming, and may necessitate the use of radiographic labeling. By contrast, luminescence technologies offer the potential for rapid, sensitive and low-cost detection that are amenable to high-throughput and real-time analysis. The discoveries of molecular beacons and aptamers have spearheaded the development of new luminescent methodologies for the detection of proteins over the last decade. We survey here recent advances in the development of luminescent detection methods for DNA-binding proteins, including those based on molecular beacons, aptamer beacons, label-free techniques and exonuclease protection.
UR - http://www.scopus.com/inward/record.url?scp=84863116694&partnerID=8YFLogxK
U2 - 10.1093/nar/gkr763
DO - 10.1093/nar/gkr763
M3 - Review article
C2 - 21967849
AN - SCOPUS:84863116694
SN - 0305-1048
VL - 40
SP - 941
EP - 955
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 3
ER -