TY - JOUR
T1 - Development of an HTS-Compatible Assay for Discovery of Melanoma-Related Microphthalmia Transcription Factor Disruptors Using AlphaScreen Technology
AU - Wang, Jing
AU - Fang, Pengfei
AU - Chase, Peter
AU - Tshori, Sagi
AU - Razin, Ehud
AU - Spicer, Timothy P.
AU - Scampavia, Louis
AU - Hodder, Peter
AU - Guo, Min
N1 - Publisher Copyright:
© 2016 Society for Laboratory Automation and Screening.
PY - 2017/1/1
Y1 - 2017/1/1
N2 - Microphthalmia transcription factor (MITF) is a master transcription factor expressed in melanocytes, essential for melanocyte survival, differentiation, and pigment formation, and is a key oncogenic factor in melanoma initiation, migration, and treatment resistance. Although identified as an important therapeutic target for melanoma, clinical inhibitors directly targeting the MITF protein are not available. Based on the functional state of MITF, we have designed an MITF dimerization-based AlphaScreen (MIDAS) assay that sensitively and specifically mirrors the dimerization of MITF in vitro. This assay is further exploited for identification of the MITF dimer disruptor for high-throughput screening. A pilot screen against a library of 1280 pharmacologically active compounds indicates that the MIDAS assay performance exhibits exceptional results with a Z′ factor of 0.81 and a signal-to-background (S/B) ratio of 3.92 while identifying initial hit compounds that yield an ability to disrupt MITF-DNA interaction. The results presented demonstrate that the MIDAS assay is ready to screen large chemical libraries in order to discover novel modulators of MITF for potential melanoma treatment.
AB - Microphthalmia transcription factor (MITF) is a master transcription factor expressed in melanocytes, essential for melanocyte survival, differentiation, and pigment formation, and is a key oncogenic factor in melanoma initiation, migration, and treatment resistance. Although identified as an important therapeutic target for melanoma, clinical inhibitors directly targeting the MITF protein are not available. Based on the functional state of MITF, we have designed an MITF dimerization-based AlphaScreen (MIDAS) assay that sensitively and specifically mirrors the dimerization of MITF in vitro. This assay is further exploited for identification of the MITF dimer disruptor for high-throughput screening. A pilot screen against a library of 1280 pharmacologically active compounds indicates that the MIDAS assay performance exhibits exceptional results with a Z′ factor of 0.81 and a signal-to-background (S/B) ratio of 3.92 while identifying initial hit compounds that yield an ability to disrupt MITF-DNA interaction. The results presented demonstrate that the MIDAS assay is ready to screen large chemical libraries in order to discover novel modulators of MITF for potential melanoma treatment.
KW - AlphaScreen
KW - MITF
KW - high-throughput screening
KW - melanoma
UR - http://www.scopus.com/inward/record.url?scp=85007189907&partnerID=8YFLogxK
U2 - 10.1177/1087057116675274
DO - 10.1177/1087057116675274
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C2 - 27827304
AN - SCOPUS:85007189907
SN - 1087-0571
VL - 22
SP - 58
EP - 66
JO - Journal of Biomolecular Screening
JF - Journal of Biomolecular Screening
IS - 1
ER -