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BioAssay: AID 1059

In Vitro HePTP Dose Response Colorimetric Assay for SAR Study

This HePTP dose response assay is developed and performed for the purpose of SAR study on analogs of hits originally identified in the HePTPcolorimetric HTS assay (AID 521). ..more
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 Tested Compounds
 Tested Compounds
All(112)
 
 
Active(57)
 
 
Inactive(55)
 
 
 Tested Substances
 Tested Substances
All(112)
 
 
Active(57)
 
 
Inactive(55)
 
 
AID: 1059
Data Source: Burnham Center for Chemical Genomics (SDCCG-A049-HePTP (In Vitro SAR-Colorimetric ))
BioAssay Type: Confirmatory, Concentration-Response Relationship Observed
Depositor Category: NIH Molecular Libraries Screening Center Network
BioAssay Version:
Deposit Date: 2008-02-28
Modify Date: 2010-10-28

Data Table ( Complete ):           Active    All
Target
BioActive Compounds: 57
Depositor Specified Assays
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AIDNameTypeProbeComment
521HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Targetconfirmatory
2085Summary assay for inhibitors of HePTPsummary2
488889SAR analysis of compounds that inhibit HePTP - Set 3confirmatory
2134HTS HePTP Fluorescent Assay using OMFP substrate for In Vitro dose response studiesconfirmatory
2678SAR analysis of chemical inhibitors of HePTP using a Fluorescent assay - Set 2confirmatory
1077Fluorescent secondary assay for dose-response confirmation of chemical inhibitors of HePTPconfirmatory
449736SAR analysis of compounds that inhibit HePTP - Set 2confirmatory
2068MOA HePTP Fluorescent secondary assay for identification of redox-state modulating compoundsconfirmatory
435032Dose Response confirmation of HTS hits from an HePTP Fluorescent Assay using OMFP substrate - Set 2confirmatory
488923Dose Response confirmation of compounds that inhibit HePTPconfirmatory
Description:
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG)
Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA)
Network: NIH Molecular Libraries Screening Centers Network (MLSCN)
Grant Number: XO1 MH077603-01
Assay Provider: Dr. Tomas Mustelin, Sanford-Burnham Medical Research Institute

This HePTP dose response assay is developed and performed for the purpose of SAR study on analogs of hits originally identified in the HePTPcolorimetric HTS assay (AID 521).

Protein tyrosine phosphatases (PTPs), working with protein tyrosine kinases (PTKs), control the phosphorylation state of many proteins in the signal transduction pathways. HePTP is a tyrosine phosphatase expressed in hematopoietic cells and regulates the MAP kinases Erk and p38. It has been found that HePTP is often dysregualted in the preleukemic disorder myelodysplastic syndrome, as well as in acute myelogeneous leukemia. Small molecule inhibitors of HePTP will be useful as molecular probes for studying the mechanism of signal transduction and MAP kinase regulation, and may have therapeutic potential for the treatment of hematopoietic malignancies.
Protocol
HePTP assay materials:
1) HePTP protein was provided by Dr. Mustelin (Sanford-Burnham Medical Research Institute, San Diego, CA). The pNPP pellets were obtained from Sigma-Aldrich (S0942). Biomol Green reagent was purchased from BIOMOL Research Laboratories, Inc (AK-111)
2) Assay Buffer: 50 mM Bis-Tris, pH 6.0, 2.5 mM DTT, 0.0125% Tween 20.
3) HePTP working solution contained 6.875 nM HePTP in assay buffer. Solution was prepared fresh prior to use.
4) pNPP working solution contained 1 mM pNPP in MQ water. Solution was prepared fresh prior to use.
5) Vanadate working solution - 45 mM Na3VO4 in 10% DMSO

HePTP dose-response protocol:
1)Dose-response curves contained 10 concentrations of compounds obtained using 2-fold serial dilution. Compounds were serially diluted in 100% DMSO, and then diluted with water to 10% final DMSO concentration. 4 uL compounds in 10% DMSO were transferred into columns 3-22 of Greiner 384-well white small-volume plates (784075). Columns 1-2 and 23-24 contained 4 uL of vanadate working solution and 10% DMSO, respectively.
2)8 uL of HePTP working solution was added to the whole plate using WellMate bulk dispenser (Matrix).
3)8 uL of pNPP working solution was added to the whole plate using WellMate bulk dispenser (Matrix).
4)Plates were incubated for 1h at room temperature.
5)Absorbance at 620 nM was measured on the Envision plate reader (PerkinElmer).
6)Data analysis was performed using CBIS software (ChemInnovations, Inc) using sigmoidal dose-response equation through non-linear regression
Comment
A positive of the assay is defined as a compound with IC50 value in the range of tested concentrations, i.e. below 100 uM.

Activity scoring rules developed at Sanford-Burnham Center for Chemical Genomics were devised to take into consideration compound efficacy, the screening stage of the data and apparent compound behavior in the assay. Details of the Scoring System will be published elsewhere.

Briefly, the outline of the scoring system utilized for the HePTP assay is as follows:
1) First tier (0-40 range) is reserved for primary screening data and therefore is not applicable in this assay.

2) Second tier (41-80 range) is reserved for dose-response confirmation data of the primary hits and therefore is not applicable in this assay.

3) Third tier (81-100 range) is reserved for dry-powder compounds that represent purchased and resynthesized positives and their analogues and utilized for SAR studies.
a. Compounds that failed to reproduce from dry powder or have IC50 > 100 uM are assigned inactive and a score value of 81.
b. The score is linearly correlated with a compound's potency and, in addition, provides a measure of the likelihood that the compound is not an artifact based on the available information. The Hill coefficient is taken as a measure of compound behavior in the assay via an additional scaling factor QC:
QC = 2.6*[exp(-0.5*nH^2) - exp(-1.5*nH^2)]
This empirical factor prorates the likelihood of a target- or a pathway-specific compound effect vs. its non-specific behavior in the assay. This factor is based on the expectation that a compound with a single mode of action that achieved an equilibrium in the assay would demonstrate the Hill coefficient value of 1. Compounds deviating from that behavior are penalized proportionally to the degree of their divergence.
c. The score is calculated using the following equation:
Score = 82+3*(pIC50-4)*QC,
where pIC50 is a negative log(10) of the IC50 value expressed in mole/L concentration units, and QC is calculated using Hill coefficient as above. This equation results in the Score values above 85 for compounds that demonstrate high potency and predictable behavior in the assays.
Result Definitions
TIDNameDescriptionHistogramTypeUnit
OutcomeThe BioAssay activity outcomeOutcome
ScoreThe BioAssay activity ranking scoreInteger
1IC50_QualifierThis qualifier is to be used with the next TID, IC50. If qualifier is "=", IC50 result equals to the value in that column; if qualifier is ">", IC50 result is greater than that value.String
2IC50*IC50 value determined using sigmoidal dose response equationFloatμM
3St.Err(IC50)Standard Error of IC50 valueFloatμM
4nHHill coefficient determined using sigmoidal dose response equationFloat

* Activity Concentration.

Data Table (Concise)
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