Deep indel mutagenesis reveals the impact of amino acid insertions and deletions on protein stability and function

Amino acid insertions and deletions (indels) are an abundant class of genetic variants. However, compared to substitutions, the effects of indels on protein stability are not well understood. To better understand indels here we analyse new and existing large-scale deep indel mutagenesis (DIM) of structurally diverse proteins. The effects of indels on protein stability vary extensively among and within proteins and are not well predicted by existing computational methods. To address this shortcoming we present INDELi, a series of models that combine experimental or predicted substitution effects and secondary structure information to provide good prediction of the effects of indels on both protein stability and pathogenicity. Moreover, quantifying the effects of indels on protein-protein interactions suggests that insertions can be an important class of gain-of-function variants. Our results provide an overview of the impact of indels on proteins and a method to predict their effects genome-wide.

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Publication Details

Journal
Nature Communications
Published
2025-03-17
DOI
https://doi.org/10.1038/s41467-025-57510-5
Citations
17
Primary Topic
Genomics and Phylogenetic Studies
Type
article
Field-Weighted Citation Impact
13.70

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article

Deep indel mutagenesis reveals the impact of amino acid insertions and deletions on protein stability and function

Magdalena Topolska, Ben Lehner, Antoni Beltran
17 citations
Nature Communications
Genomics and Phylogenetic Studies
13.70
article

Deep indel mutagenesis reveals the impact of amino acid insertions and deletions on protein stability and function

Magdalena Topolska, Ben Lehner, Antoni Beltran
article en
17 citations

Abstract

Amino acid insertions and deletions (indels) are an abundant class of genetic variants. However, compared to substitutions, the effects of indels on protein stability are not well understood. To better understand indels here we analyse new and existing large-scale deep indel mutagenesis (DIM) of structurally diverse proteins. The effects of indels on protein stability vary extensively among and within proteins and are not well predicted by existing computational methods. To address this shortcoming we present INDELi, a series of models that combine experimental or predicted substitution effects and secondary structure information to provide good prediction of the effects of indels on both protein stability and pathogenicity. Moreover, quantifying the effects of indels on protein-protein interactions suggests that insertions can be an important class of gain-of-function variants. Our results provide an overview of the impact of indels on proteins and a method to predict their effects genome-wide.

Nature CommunicationsVol. 16(1)
Institució Catalana de Recerca i Estudis Avançats (ES), Universitat Pompeu Fabra (ES), Wellcome Sanger Institute (GB), Centre for Genomic Regulation (ES)
Centres de Recerca de Catalunya, AXA Research Fund, Generalitat de Catalunya, Ministerio de Ciencia e Innovación, Fondation Bettencourt Schueller, Agència de Gestió d'Ajuts Universitaris i de Recerca
Openalex Percentile: Top 1%
Genomics and Phylogenetic Studies
13.70
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