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ATM Kinase

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Cover of 'ATM Kinase'

Table of Contents

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    Book Overview
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    Chapter 1 Assaying Radiosensitivity of Ataxia-Telangiectasia
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    Chapter 2 Assaying for Radioresistant DNA Synthesis, the Hallmark Feature of the Intra-S-Phase Checkpoint Using a DNA Fiber Technique
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    Chapter 3 ATM Gene Mutation Detection Techniques and Functional Analysis
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    Chapter 4 An HTRF® Assay for the Protein Kinase ATM
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    Chapter 5 ATM Kinase Inhibitors: HTS Cellular Imaging Assay Using Cellomics™ ArrayScan VTI Platform
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    Chapter 6 Image-Based High Content Screening: Automating the Quantification Process for DNA Damage-Induced Foci
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    Chapter 7 Analyzing ATM Function by Electroporation of Endonucleases and Immunofluorescence Microscopy
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    Chapter 8 Quantitative and Dynamic Imaging of ATM Kinase Activity by Bioluminescence Imaging
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    Chapter 9 Zn(II)–Phos-Tag SDS-PAGE for Separation and Detection of a DNA Damage-Related Signaling Large Phosphoprotein
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    Chapter 10 Identification of ATM Protein Kinase Phosphorylation Sites by Mass Spectrometry
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    Chapter 11 Studies of ATM Kinase Activity Using Engineered ATM Sensitive to ATP Analogues (ATM-AS)
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    Chapter 12 Functional Characterization of ATM Kinase Using Acetylation-Specific Antibodies
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    Chapter 13 Identification of ATM-Interacting Proteins by Co-immunoprecipitation and Glutathione-S-Transferase (GST) Pull-Down Assays
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    Chapter 14 ATM Activation and H2AX Phosphorylation Induced by Genotoxic Agents Assessed by Flow- and Laser Scanning Cytometry
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    Chapter 15 Peptide Immunoaffinity Enrichment with Targeted Mass Spectrometry: Application to Quantification of ATM Kinase Phospho-Signaling
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    Chapter 16 Mass Spectrometry-Based Proteomics for Quantifying DNA Damage-Induced Phosphorylation
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    Chapter 17 Statistical Analysis of ATM-Dependent Signaling in Quantitative Mass Spectrometry Phosphoproteomics
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    Chapter 18 ChIP Technique to Study Protein Dynamics at Defined DNA Double Strand Breaks
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    Chapter 19 Studies of the DNA Damage Response by Using the Lac Operator/Repressor (LacO/LacR) Tethering System
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    Chapter 20 Imaging of Fluorescently Tagged ATM Kinase at the Sites of DNA Double Strand Breaks
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    Chapter 21 Live Cell Imaging to Study Real-Time ATM-Mediated Recruitment of DNA Repair Complexes to Sites of Ionizing Radiation-Induced DNA Damage
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    Chapter 22 Analyzing Heterochromatic DNA Double Strand Break (DSB) Repair in Response to Ionizing Radiation
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    Chapter 23 Phenotypic Analysis of ATM Protein Kinase in DNA Double-Strand Break Formation and Repair
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    Chapter 24 Monitoring DNA Repair Consequences of ATM Signaling Using Simultaneous Fluorescent Readouts
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    Chapter 25 Noncanonical ATM Activation and Signaling in Response to Transcription-Blocking DNA Damage
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    Chapter 26 Study of ATM Phosphorylation by Cdk5 in Neuronal Cells
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    Chapter 27 DNA Damage Response in Human Stem Cells and Neural Descendants
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    Chapter 28 A Patient-Specific Stem Cell Model to Investigate the Neurological Phenotype Observed in Ataxia-Telangiectasia
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    Chapter 29 Lentiviral Reprogramming of A-T Patient Fibroblasts to Induced Pluripotent Stem Cells
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    Chapter 30 Monitoring the ATM-Mediated DNA Damage Response in the Cerebellum Using Organotypic Cultures
Attention for Chapter 21: Live Cell Imaging to Study Real-Time ATM-Mediated Recruitment of DNA Repair Complexes to Sites of Ionizing Radiation-Induced DNA Damage
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Chapter title
Live Cell Imaging to Study Real-Time ATM-Mediated Recruitment of DNA Repair Complexes to Sites of Ionizing Radiation-Induced DNA Damage
Chapter number 21
Book title
ATM Kinase
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6955-5_21
Pubmed ID
Book ISBNs
978-1-4939-6953-1, 978-1-4939-6955-5
Authors

Burkhard Jakob, Gisela Taucher-Scholz

Editors

Sergei V. Kozlov

Abstract

Measurements of protein recruitment and the formation of repair complexes at DNA double-strand breaks in real time provide valuable insight into the regulation of the early DNA damage response. Here, we describe the use of live cell microscopy in combination with ionizing radiation as a tool to evaluate the influence of ATM and its site-specific phosphorylation of target proteins on these processes. Recommendations are made for the preparation of the cells and the design of specialized cell chambers for the localized (and/or targeted) irradiation with charged particles at accelerator beamlines as well as the microscopic equipment and protocol to obtain high-resolution, sensitive fluorescence measurements.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 27%
Student > Master 2 18%
Student > Bachelor 2 18%
Student > Ph. D. Student 1 9%
Unspecified 1 9%
Other 0 0%
Unknown 2 18%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 36%
Unspecified 1 9%
Medicine and Dentistry 1 9%
Neuroscience 1 9%
Chemistry 1 9%
Other 1 9%
Unknown 2 18%