Normalized and Directional Interplay Scoring for the Interrogation of Proteoform Data

Histone proteoforms, often presenting multiple co-occurring post-translational modifications (PTMs), are central to chromatin regulation and gene expression. A proteoform is a specific form of a protein that includes variations arising from genetic changes, alternative RNA splicing, proteolytic processing, and PTMs. Genome-indexed histone proteoforms define the histone code, influencing cellular phenotype by dictating DNA interacting partners. Understanding the dynamics of histone proteoforms is essential for elucidating chromatin-based regulatory mechanisms. Advances in middle-down and top-down proteomics enable accurate identification and quantitation of thousands of proteoforms in a single run. However, the resulting data complexity presents significant challenges for analysis and visualization. Here, we introduce two new computational methods to analyze the dynamics of histone PTMs and demonstrate their use in mouse organs during aging. The score that we term "normalized interplay" addresses limitations of the original crosstalk score "interplay" providing a more complete and accurate measure of PTM crosstalk. The second score, Δ<i>I</i> or "directional interplay" is an asymmetric measure quantifying the magnitude and directionality of crosstalk between PTMs. Applying our two-stage scoring approach to data from CrosstalkDB reveals the dynamics of histone H3 modifications during aging.

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Publication Details

Journal
Journal of Proteome Research
Published
2025-02-28
DOI
https://doi.org/10.1021/acs.jproteome.4c00877
Citations
2
Primary Topic
Advanced Malware Detection Techniques
Type
article
Field-Weighted Citation Impact
2.97

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article

Normalized and Directional Interplay Scoring for the Interrogation of Proteoform Data

Nicolas L. Young, Alyssa T. Paparella, Karl F. Poncha
2 citations
Journal of Proteome Research
Advanced Malware Detection Techniques
2.97
article

Normalized and Directional Interplay Scoring for the Interrogation of Proteoform Data

Nicolas L. Young, Alyssa T. Paparella, Karl F. Poncha
article en
2 citations

Abstract

Histone proteoforms, often presenting multiple co-occurring post-translational modifications (PTMs), are central to chromatin regulation and gene expression. A proteoform is a specific form of a protein that includes variations arising from genetic changes, alternative RNA splicing, proteolytic processing, and PTMs. Genome-indexed histone proteoforms define the histone code, influencing cellular phenotype by dictating DNA interacting partners. Understanding the dynamics of histone proteoforms is essential for elucidating chromatin-based regulatory mechanisms. Advances in middle-down and top-down proteomics enable accurate identification and quantitation of thousands of proteoforms in a single run. However, the resulting data complexity presents significant challenges for analysis and visualization. Here, we introduce two new computational methods to analyze the dynamics of histone PTMs and demonstrate their use in mouse organs during aging. The score that we term "normalized interplay" addresses limitations of the original crosstalk score "interplay" providing a more complete and accurate measure of PTM crosstalk. The second score, Δ<i>I</i> or "directional interplay" is an asymmetric measure quantifying the magnitude and directionality of crosstalk between PTMs. Applying our two-stage scoring approach to data from CrosstalkDB reveals the dynamics of histone H3 modifications during aging.

Journal of Proteome ResearchVol. 24(4)
Baylor College of Medicine (US)
Howard Hughes Medical Institute, National Institute on Aging, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke
Zero hunger
Openalex Percentile: Top 11%
Advanced Malware Detection Techniques
2.97
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Normalized and Directional Interplay Scoring for the Interrogation of Proteoform Data — Nicolas L. Young, Alyssa T. Paparella, et al. · Journal of Proteome Research (2025) | TGRS Research Map | TGRS