Literature DB >> 28809825

Analysis of Histone Antibody Specificity with Peptide Microarrays.

Evan M Cornett1, Bradley M Dickson1, Scott B Rothbart2.   

Abstract

Post-translational modifications (PTMs) on histone proteins are widely studied for their roles in regulating chromatin structure and gene expression. The mass production and distribution of antibodies specific to histone PTMs has greatly facilitated research on these marks. As histone PTM antibodies are key reagents for many chromatin biochemistry applications, rigorous analysis of antibody specificity is necessary for accurate data interpretation and continued progress in the field. This protocol describes an integrated pipeline for the design, fabrication and use of peptide microarrays for profiling the specificity of histone antibodies. The design and analysis aspects of this procedure are facilitated by ArrayNinja, an open-source and interactive software package we recently developed to streamline the customization of microarray print formats. This pipeline has been used to screen a large number of commercially available and widely used histone PTM antibodies, and data generated from these experiments are freely available through an online and expanding Histone Antibody Specificity Database. Beyond histones, the general methodology described herein can be applied broadly to the analysis of PTM-specific antibodies.

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Year:  2017        PMID: 28809825      PMCID: PMC5613814          DOI: 10.3791/55912

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  50 in total

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3.  SnapShot: histone modifications.

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4.  The histone-H3K4-specific demethylase KDM5B binds to its substrate and product through distinct PHD fingers.

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Journal:  Cell Rep       Date:  2014-01-09       Impact factor: 9.423

5.  Bottom-up and middle-down proteomics have comparable accuracies in defining histone post-translational modification relative abundance and stoichiometry.

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6.  Combinatorial profiling of chromatin binding modules reveals multisite discrimination.

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8.  DNA methylation presents distinct binding sites for human transcription factors.

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9.  Poly-acetylated chromatin signatures are preferred epitopes for site-specific histone H4 acetyl antibodies.

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Authors:  Rohan N Shah; Adrian T Grzybowski; Evan M Cornett; Andrea L Johnstone; Bradley M Dickson; Brandon A Boone; Marcus A Cheek; Martis W Cowles; Danielle Maryanski; Matthew J Meiners; Rochelle L Tiedemann; Robert M Vaughan; Neha Arora; Zu-Wen Sun; Scott B Rothbart; Michael-Christopher Keogh; Alexander J Ruthenburg
Journal:  Mol Cell       Date:  2018-09-20       Impact factor: 17.970

2.  Study of mitotic chromatin supports a model of bookmarking by histone modifications and reveals nucleosome deposition patterns.

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3.  A Degenerate Peptide Library Approach to Reveal Sequence Determinants of Methyllysine-Driven Protein Interactions.

Authors:  Ariana Kupai; Robert M Vaughan; Bradley M Dickson; Scott B Rothbart
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4.  A trivalent nucleosome interaction by PHIP/BRWD2 is disrupted in neurodevelopmental disorders and cancer.

Authors:  Marc A J Morgan; Irina K Popova; Anup Vaidya; Jonathan M Burg; Matthew R Marunde; Emily J Rendleman; Zachary J Dumar; Rachel Watson; Matthew J Meiners; Sarah A Howard; Natalia Khalatyan; Robert M Vaughan; Scott B Rothbart; Michael-C Keogh; Ali Shilatifard
Journal:  Genes Dev       Date:  2021-11-24       Impact factor: 12.890

5.  ARID1A-dependent maintenance of H3.3 is required for repressive CHD4-ZMYND8 chromatin interactions at super-enhancers.

Authors:  Jake J Reske; Mike R Wilson; Brooke Armistead; Shannon Harkins; Cristina Perez; Joel Hrit; Marie Adams; Scott B Rothbart; Stacey A Missmer; Asgerally T Fazleabas; Ronald L Chandler
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6.  A physical basis for quantitative ChIP-sequencing.

Authors:  Bradley M Dickson; Rochelle L Tiedemann; Alison A Chomiak; Evan M Cornett; Robert M Vaughan; Scott B Rothbart
Journal:  J Biol Chem       Date:  2020-09-29       Impact factor: 5.157

  6 in total

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