(Q33361565)

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Development, validation and implementation of immobilized metal affinity for phosphochemicals (IMAP)-based high-throughput screening assays for low-molecular-weight compound libraries

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Europe PubMed Central

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26 July 2017

Development, validation and implementation of immobilized metal affinity for phosphochemicals (IMAP)-based high-throughput screening assays for low-molecular-weight compound libraries (English)

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Europe PubMed Central

PubMed publication ID

26 July 2017

6

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John S Lazo

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Europe PubMed Central

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26 July 2017

Elizabeth R Sharlow

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object named as

Elizabeth R Sharlow

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Europe PubMed Central

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26 July 2017

Stephanie Leimgruber

2

object named as

Stephanie Leimgruber

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26 July 2017

Rebecca E Sutter-Barrett

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object named as

Rebecca Barrett

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26 July 2017

Qiming Jane Wang

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object named as

Qiming Jane Wang

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26 July 2017

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Archibong Yellow-Duke

3

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26 July 2017

publication date

1 January 2008

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26 July 2017

Nature Protocols

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26 July 2017

3

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26 July 2017

8

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26 July 2017

1350-1363

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Europe PubMed Central

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26 July 2017

https://scigraph.springernature.com/pub.10.1038/nprot.2008.111

0 references

High-throughput screening assays for the identification of chemical probes

1 reference

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High-throughput screening: new technology for the 21st century

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Fluorescence technologies for the investigation of chemical libraries

1 reference

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Origin and evolution of high throughput screening

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High-throughput screening: update on practices and success

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Drug discovery in academia

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NIH Molecular Libraries Initiative

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Roadmap or roadkill: a pharmacologist's analysis of the NIH Molecular Libraries Initiative

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Innovative lead discovery strategies for tropical diseases

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Potent, selective and cell penetrant inhibitors of SF-1 by functional ultra-high-throughput screening

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Development and implementation of a miniaturized high-throughput time-resolved fluorescence energy transfer assay to identify small molecule inhibitors of polo-like kinase 1.

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Oncogenic kinase signalling

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Protein kinases--the major drug targets of the twenty-first century?

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The protein kinase complement of the human genome

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Fluorescence readouts in HTS: no gain without pain?

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Identification of small molecule ceramide kinase inhibitors using a homogeneous chemiluminescence high throughput assay

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High-throughput screening with quantitation of ATP consumption: a universal non-radioisotope, homogeneous assay for protein kinase

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An enzyme-linked immunosorbent assay for protein kinase D activity using phosphorylation site-specific antibodies.

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Development of a non-radioactive, 384-well format assay to detect inhibitors of the mitogen-activated protein kinase kinase 4.

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Highly sensitive fluorescence detection technology currently available for HTS.

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A generic high-throughput screening assay for kinases: protein kinase a as an example

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Homogeneous fluorescence readouts for miniaturized high-throughput screening: theory and practice

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A fluorescence polarization assay for native protein substrates of kinases

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Development of a Transcreener kinase assay for protein kinase A and demonstration of concordance of data with a filter-binding assay format

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Comparison of miniaturized time-resolved fluorescence resonance energy transfer and enzyme-coupled luciferase high-throughput screening assays to discover inhibitors of Rho-kinase II (ROCK-II).

1 reference

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Three mechanistically distinct kinase assays compared: Measurement of intrinsic ATPase activity identified the most comprehensive set of ITK inhibitors

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Assay concordance between SPA and TR-FRET in high-throughput screening

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Evaluation of assay technologies for the identification of protein-Peptide interaction antagonists.

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Metal ion-mediated polymer superquenching for highly sensitive detection of kinase and phosphatase activities

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A homogeneous fluorescence polarization assay adaptable for a range of protein serine/threonine and tyrosine kinases

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Immobilized metal ion affinity-based fluorescence polarization (IMAP): advances in kinase screening

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High-throughput screening with immobilized metal ion affinity-based fluorescence polarization detection, a homogeneous assay for protein kinases

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Considerations for using fluorescence polarization in the screening of G protein-coupled receptors

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Development of a fluorescence polarization AKT serine/threonine kinase assay using an immobilized metal ion affinity-based technology

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Readout technologies for highly miniaturized kinase assays applicable to high-throughput screening in a 1536-well format.

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Development of a fluorescence polarization bead-based coupled assay to target different activity/conformation states of a protein kinase

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Targeting polo-like kinase 1 for cancer therapy.

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ON01910, a non-ATP-competitive small molecule inhibitor of Plk1, is a potent anticancer agent.

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BI 2536, a potent and selective inhibitor of polo-like kinase 1, inhibits tumor growth in vivo.

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PKD at the crossroads of DAG and PKC signaling

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Protein kinase d in the cardiovascular system: emerging roles in health and disease.

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Development and optimization of high-throughput in vitro protein phosphatase screening assays

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Determining appropriate substrate conversion for enzymatic assays in high-throughput screening

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Establishment and application of a high throughput model for Rho kinase inhibitors screening based on fluorescence polarization.

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Miniaturized, ultra-high throughput screening of tyrosine kinases using homogeneous, competitive fluorescence immunoassays

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A Simple Statistical Parameter for Use in Evaluation and Validation of High Throughput Screening Assays

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HTS identifies novel and specific uncompetitive inhibitors of the two-component NS2B-NS3 proteinase of West Nile virus

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Development and implementation of a 384-well homogeneous fluorescence intensity high-throughput screening assay to identify mitogen-activated protein kinase phosphatase-1 dual-specificity protein phosphatase inhibitors

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An improved method for checking HTS/uHTS liquid-handling systems

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Identifiers

10.1038/NPROT.2008.111

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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