TY - JOUR
T1 - New assay technologies for high-throughput screening
AU - Silverman, Lauren
AU - Campbell, Robert
AU - Broach, James R.
PY - 1998/6
Y1 - 1998/6
N2 - The use of high-throughput screening for early stage drug discovery imposes several constraints on the format of assays for therapeutic targets of interest. Homogeneous cell-free assays based on energy transfer, fluorescence polarization spectroscopy or fluorescence correlation spectroscopy provide the sensitivity, ease, speed and resistance to interference from test compounds needed to function in a high-throughput screening mode. Similarly, novel cell-based assays are now being adapted for high-throughput screening, providing for in situ analysis of a variety of biological targets. Finally, recent advances in assay miniaturization mark a transition to ultra high-throughput screening, ensuring that identification of lead compounds will not be the rate-limiting step in finding new drugs.
AB - The use of high-throughput screening for early stage drug discovery imposes several constraints on the format of assays for therapeutic targets of interest. Homogeneous cell-free assays based on energy transfer, fluorescence polarization spectroscopy or fluorescence correlation spectroscopy provide the sensitivity, ease, speed and resistance to interference from test compounds needed to function in a high-throughput screening mode. Similarly, novel cell-based assays are now being adapted for high-throughput screening, providing for in situ analysis of a variety of biological targets. Finally, recent advances in assay miniaturization mark a transition to ultra high-throughput screening, ensuring that identification of lead compounds will not be the rate-limiting step in finding new drugs.
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U2 - 10.1016/S1367-5931(98)80015-X
DO - 10.1016/S1367-5931(98)80015-X
M3 - Article
C2 - 9691081
AN - SCOPUS:0032087370
SN - 1367-5931
VL - 2
SP - 397
EP - 403
JO - Current Opinion in Chemical Biology
JF - Current Opinion in Chemical Biology
IS - 3
ER -