Bookmark and Share
BioAssay: AID 1534

Dose response biochemical high throughput screening assay for inhibitors of the p97 ATPase

Misfolded proteins accumulate in the endoplasmic reticulum (ER) in response to environmental stress (1). To reduce the burden these proteins place on the secretory pathway, eukaryotic cells have evolved a process, known as ER-associated degradation (ERAD), to recognize and eliminate these proteins (1, 2). The highly conserved p97 ATPase functions in ERAD by hydrolyzing ATP needed to export more ..
_
   
 Tested Compounds
 Tested Compounds
All(54)
 
 
Active(5)
 
 
Inactive(49)
 
 
 Tested Substances
 Tested Substances
All(54)
 
 
Active(5)
 
 
Inactive(49)
 
 
AID: 1534
Data Source: The Scripps Research Institute Molecular Screening Center (P97_INH_LUMI_384_IC50)
BioAssay Type: Confirmatory, Concentration-Response Relationship Observed
Depositor Category: NIH Molecular Libraries Probe Production Network
Deposit Date: 2009-03-04

Data Table ( Complete ):           View Active Data    View All Data
Target
BioActive Compounds: 5
Related Experiments
Show more
AIDNameTypeProbeComment
1481Primary biochemical high-throughput screening assay to measure P97 ATPase inhibitionScreening depositor-specified cross reference
1517Confirmation biochemical high-throughput screening assay for inhibitors of the p97 ATPaseScreening depositor-specified cross reference
1794Summary of probe development efforts to identify inhibitors of the p97 ATPase.Summary1 depositor-specified cross reference
2131Late stage results from the probe development effort to identify inhibitors of the p97 ATPase.Screening depositor-specified cross reference
463184p97 ATPase dose responseConfirmatory depositor-specified cross reference
463185Inhibition of proteasomal turnover of a p97-dependent reporter substrate in human cellsConfirmatory depositor-specified cross reference
488828p97 ATPase dose response - Hit Optimization Round 2Confirmatory depositor-specified cross reference
488830Inhibition of proteasomal turnover of a p97-dependent reporter substrate in human cells - Hit Optimization Round 2Confirmatory depositor-specified cross reference
504649Inhibition of proteasomal turnover of a p97-dependent reporter substrate in human cells - Hit Optimization Round 3Confirmatory depositor-specified cross reference
504650p97 ATPase dose response - Hit Optimization Round 3Confirmatory depositor-specified cross reference
504653Caspase 3/7 Activation in response to p97 inhibitionOther depositor-specified cross reference
504654Inhibition of p97-independent reporter turnoverConfirmatory depositor-specified cross reference
1544Luminescence counterscreen assay for p97 inhibitors: Dose response biochemical high throughput screening assay to identify inhibitors of the C522A mutant p97 ATPase.Confirmatory same project related to Summary assay
1551Luminescence dose response biochemical high throughput screening assay for inhibitors of the p97 ATPase: synthesized compounds.Confirmatory same project related to Summary assay
1629Luminescence counterscreen assay for p97 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of the C522A mutant p97 ATPase: synthesized compounds.Confirmatory same project related to Summary assay
Description:
Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center
Center Affiliation: The Scripps Research Institute (TSRI)
Assay Provider: Raymond Deshaies, California Institute of Technology
Network: Molecular Libraries Probe Production Centers Network (MLPCN)
Grant Proposal Number: 1 R03 MH085687-01
Grant Proposal PI: Raymond Deshaies, California Institute of Technology
External Assay ID: p97_INH_Lumi_384_IC50

Name: Dose response biochemical high throughput screening assay for inhibitors of the p97 ATPase

Description:

Misfolded proteins accumulate in the endoplasmic reticulum (ER) in response to environmental stress (1). To reduce the burden these proteins place on the secretory pathway, eukaryotic cells have evolved a process, known as ER-associated degradation (ERAD), to recognize and eliminate these proteins (1, 2). The highly conserved p97 ATPase functions in ERAD by hydrolyzing ATP needed to export ubiquitinated substrates to the cytosol for degradation by the proteasome (2, 3). The discovery of p97 missense mutations in a genetic form of human dementia (5-7), the localization of p97 in ubiquitylated inclusions in affected neurons of amyotrophic lateral sclerosis (ALS) and Parkinson's disease (8-9), and the overproduction of p97 in multiple cancers (10-14), suggests that p97 has diverse and essential cellular roles. Thus, the identification of probes that selectively target p97 activity may provide insights into the biological roles of p97.

References:

1. Raasi S, Wolf DH. Ubiquitin receptors and ERAD: a network of pathways to the proteasome. Semin Cell Dev Biol. 2007 Dec;18(6):780-91.
2. Halawani D, Latterich M. p97: The cell's molecular purgatory? Mol Cell. 2006 (22)6: 713-717.
3. Wang Q, Li L, Ye Y. Inhibition of p97-dependent protein degradation by Eeyarestatin I. J Biol Chem. 2008 Mar 21;283(12):7445-54.
4. Ye, Y., Meyer, H. H., and Rapoport, T. A., The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol. Nature. 2001. 414(6864): p. 52-656.
5. Watts, G.D., J. Wymer, M.J. Kovach, S.G. Mehta, S. Mumm, D. Darvish, A. Pestronk, M.P. Whyte, and V.E. Kimonis, Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. Nat Genet. 2004. 36(4): p. 377-81.
6. Weihl, C.C., Dalal, S., Pestronk, A., and Hanson, P. I., Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation. Hum. Mol. Genet. 2006. 15(2): p. 189-199.
7. Mizuno, Y., Hori, S., Kakizuka, A. and Okamoto, K. (2003) Vacuole-creating protein in neurodegenerative diseases in humans. Neurosci. Lett. 343, 77-80.
8. Ishigaki S, Hishikawa N, Niwa J, Iemura S, Natsume T, Hori S, Kakizuka A, Tanaka K, Sobue G. (2004) Physical and functional interaction between Dorfin and Valosin-containing protein that are colocalized in ubiquitylated inclusions in neurodegenerative disorders. J Biol Chem. 2004 Dec 3;279(49):51376-85.
9. Hirabayashi, M., Inoue, K., Tanaka, K., Nakadate, K., Ohsawa, Y., Kamei, Y., Popiel, A.H., Sinohara, A., Iwamatsu, A., Kimura, Y. Uchiyama, Y.,Hori, S., Kakizuka, A. VCP/p97 in abnormal protein aggregates, cytoplasmic vacuoles, and cell death, phenotypes relevant to neurodegeneration. Cell Death Differ. 2001, 8, 977-984.
10. Mitas, M., Mikhitarian, K., Walters, C., Baron, P. L., Elliott, B. M., Brothers, T. E., Robison, J. G., Metcalf, J. S., Palesch, Y. Y., Zhang, Z., Gillanders, W. E., and Cole, D. J., Quantitative real-time RT-PCR detection of breast cancer micrometastasis using a multigene marker panel. Int. J. Cancer. 2001. 93(2): p. 162-171.
11. Marchetti, A., Buttitta, F., Bertacca, G., Zavaglia, K., Bevilacqua, G., Angelucci, D., Viacava, P., Naccarato, A., Bonadio, A., Barassi, F., Felicioni, L., Salvatore, S., Mucilli, F., mRNA markers of breast cancer nodal metastases: comparison between mammaglobin and carcinoembryonic antigen in 248 patients. J. Pathol. 2001. 195(2): p. 186-190.
12. Smith, L.M., Nesterova, A., Alley, S. C., Torgov, M. Y., Carter, P. J., Potent cytotoxicity of an auristatin-containing antibody-drug conjugate targeting melanoma cells expressing melanotransferrin/p97. Mol. Cancer Ther, 2006. 5(6): p.1474-1482.
13. Yamamoto, S., Tomita, Y., Uruno, T., Hoshida, Y., Qiu, Y., Iizuka, N., Nakamichi, I., Miyauchi, A., and Aozasa, K., Increased expression of valosin-containing protein (p97) is correlated with disease recurrence in follicular thyroid cancer. Ann. Surg. Oncol., 2005. 12(11): p. 925-934.
14. Yamamoto, S., Tomita, Y., Uruno, T., Hoshida, Y., Qiu, Y., Iizuka, N., Nakamichi, I., Miyauchi, A., and Aozasa, K., Expression level of valosin-containing protein (p97) is associated with prognosis of esophageal carcinoma. Clin. Cancer Res., 2004. 10(16): p. 5558-5565.


Keywords:

p97, ATPase, valosin-containing protein, VCP, cancer, neurodegenerative disease, dose response, screen, 384, inhibitor, luciferase, Scripps, Scripps Florida, The Scripps Research Institute Molecular Screening Center, SRIMSC, Molecular Libraries Probe Production Centers Network, MLPCN.
Protocol
Assay Overview:
The purpose of this assay is to determine dose response curves for compounds identified as active in a previous set of experiments entitled, "Primary biochemical high-throughput screening assay to measure p97 ATPase inhibition" (PubChem AID 1481), and that confirmed activity in a subsequent set of experiments entitled, "Confirmation biochemical high-throughput screening assay for inhibitors of the p97 ATPase" (PubChem AID 1517). This biochemical assay employs the Kinase-Glo reagent, which contains a luciferase that emits luminescence in direct proportion to ATP levels. As designed, compounds that inhibit the ATPase activity of p97 will reduce ATP hydrolysis, thereby increasing the relative levels of ATP available for consumption by luciferase, resulting in increased well luminescence. Compounds were tested in triplicate using a 10-point, 1:3 dilution series, starting at a nominal concentration of 50 uM.
Protocol Summary:
Prior to the start of the assay 18 ul of Assay Buffer (1 mM DTT, 50 mM Tris HCl, 20 mM MgCl2, 1 mM EDTA, pH 8.0, filtered at 0.22 micrometer) were dispensed into columns 1 and 2, rows O and P of 384-well assay plates. The remaining wells were filled with 18 ul of Assay Buffer supplemented with 0.42 uM p97 protein. Next, 50 nL of test compounds or DMSO alone (0.8% final concentration) were distributed into the appropriate wells. The plates were then incubated for 15 minutes at 25 degrees Celsius. The assay was started by the addition of 1 ul of 10 mM Tris supplemented with 100 uM ATP to all wells. The plates were then incubated for 1 hour at 25 degrees Celsius. After incubation, 20 ul of Kinase Glo reagent were added to all 24 columns and plates were incubated for another 10 minutes at 25 degrees Celsius. Plates were centrifuged and luminescence was measured by the Envision microplate reader.
The percent inhibition for each compound was calculated using the following mathematical expression:
% Inhibition = [1-(Test_Compound - Median_High_Control) / (Median_Low_Control - Median_High_Control)]*100
Where:
Test_Compound is defined as wells containing test compound,
Low_Control is defined as wells containing DMSO,
High_Control is defined as wells containing no p97 protein.
For each test compound, percent inhibition was plotted against compound concentration. A four parameter equation describing a sigmoidal dose-response curve was then fitted with adjustable baseline using Assay Explorer software (MDL Information Systems). The reported IC50 values were generated from fitted curves by solving for the X-intercept value at the 50% inhibition level of the Y-intercept value. In cases where the highest concentration tested (i.e. 50 uM) did not result in greater than 50% inhibition, the IC50 was determined manually as greater than 50 uM. Compounds with an IC50 greater than 10 uM were considered inactive. Compounds with an IC50 equal to or less than 10 uM were considered active.
Any compound with a percent inhibition value <50% at all test concentrations was assigned an activity score of zero. Any compound with a percent inhibition value >50% at any test concentration was assigned an activity score greater than zero. Activity score was then ranked by the potency, with the most potent compounds assigned the highest activity scores.
Activity score for the active compounds of this assay have range of 22 to 100 and all inactive compounds are assigned activity score of zero.
List of Reagents:
Recombinant p97 protein (produced in the Deshaies Laboratory)
Magnesium Chloride (Fisher, part M33-500)
1M Tris, pH 8.0 (Invitrogen, part T-3038)
0.5M EDTA (Invitrogen, part 15575-025)
Dithiothreitol (Fisher, part BP172-25)
3N Sodium Acetate pH 5.2 (Sigma, part S7899)
ATP (Sigma, part A7699-1G)
Kinase-Glo (Promega, part K1214)
Methanol (Fisher, part A412-4)
DMSO (Acros Organics, part 127790025)
384-well Plates (Corning, part 3704)
Comment
Due to the increasing size of the MLPCN compound library, this assay may have been run as two or more separate campaigns, each campaign testing a unique set of compounds. Possible artifacts of this assay can include, but are not limited to: dust or lint located in or on wells of the microtiter plate, compounds that non-specifically modulate ATP hydrolysis, and compounds that quench or emit luminescence within the well. All test compound concentrations reported are nominal; the specific concentration for a particular test compound may vary based upon the actual sample provided by the MLSMR.
Categorized Comment - additional comments and annotations
From ChEMBL:
Assay Type: Binding
Result Definitions
Show more
TIDNameDescriptionHistogramTypeUnit
OutcomeThe BioAssay activity outcomeOutcome
ScoreThe BioAssay activity ranking scoreInteger
1QualifierActivity Qualifier identifies if the resultant data IC50 came from a fitted curve or was determined manually to be less than or greater than its listed IC50 concentration.String
2IC50*The concentration at which 50 percent of the activity in the inhibitor assay is observed; (IC50) shown in micromolar.FloatμM
3LogIC50Log10 of the qualified IC50 (IC50) from the inhibitor assay in M concentrationFloat
4Hill SlopeThe variable HillSlope describes the steepness of the curve. This variable is called the Hill slope, the slope factor, or the Hill coefficient. If it is positive, the curve increases as X increases. If it is negative, the curve decreases as X increases. A standard sigmoid dose-response curve (previous equation) has a Hill Slope of 1.0. When HillSlope is less than 1.0, the curve is more shallow. When HillSlope is greater than 1.0, the curve is steeper. The Hill slope has no units.Float
5Hill S0Y-min of the curve.Float
6Hill SinfY-max of the curve.Float
7Hill dSThe range of Y.Float
8Chi SquareA measure for the 'goodness' of a fit. The chi-square test (Snedecor and Cochran, 1989) is used to test if a sample of data came from a population with a specific distribution.Float
9RsquareThis statistic measures how successful the fit explains the variation of the data; R-square is the square of the correlation between the response values and the predicted response values.Float
10Number of DataPointsOverall number of data points of normalized percent inhibition that was used for calculations (includes all concentration points); in some cases a data point can be excluded as outlier.Integer
11Inhibition at 2.5 nM (0.0025μM**)Value of %inhibition at 2.5 nanomolar inhibitor concentration; average of triplicate measurement.Float%
12Inhibition at 7.6 nM (0.0076μM**)Value of %inhibition at 7.6 nanomolar inhibitor concentration; average of triplicate measurement.Float%
13Inhibition at 22.8 nM (0.0228μM**)Value of %inhibition at 22.8 nanomolar inhibitor concentration; average of triplicate measurement.Float%
14Inhibition at 68.3 nM (0.0683μM**)Value of %inhibition at 68.3 nanomolar inhibitor concentration; average of triplicate measurement.Float%
15Inhibition at 204.7 nM (0.2047μM**)Value of %inhibition at 204.7 nanomolar inhibitor concentration; average of triplicate measurement.Float%
16Inhibition at 0.6 uM (0.6μM**)Value of %inhibition at 0.6 micromolar inhibitor concentration; average of triplicate measurement.Float%
17Inhibition at 1.8 uM (1.8μM**)Value of %inhibition at 1.8 micromolar inhibitor concentration; average of triplicate measurement.Float%
18Inhibition at 5.5 uM (5.5μM**)Value of %inhibition at 5.5 micromolar inhibitor concentration; average of triplicate measurement.Float%
19Inhibition at 16.6 uM (16.6μM**)Value of %inhibition at 16.6 micromolar inhibitor concentration; average of triplicate measurement.Float%
20Inhibition at 49.8 uM (49.8μM**)Value of %inhibition at 49.8 micromolar inhibitor concentration; average of triplicate measurement.Float%

* Activity Concentration. ** Test Concentration.
Additional Information
Grant Number: 1 R03 MH085687-01

Data Table (Concise)
Data Table ( Complete ):     View Active Data    View All Data
PageFrom: