Decoding phospho-regulation and flanking regions in autophagy-associated short linear motifs

Abstract Short Linear Motifs (SLiMs) play a pivotal role in the interactions between intrinsically disordered proteins and their binding partners. SLiMs can undergo regulation through post-translational modifications, including phosphorylation. The flanking regions surrounding the core motifs also e...

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Main Authors: Mattia Utichi, Oana N. Antonescu, Valentina Sora, Henri-Baptiste Marjault, Matteo Tiberti, Emiliano Maiani, Matteo Lambrughi, Elena Papaleo
Format: Article
Language:English
Published: Nature Portfolio 2025-08-01
Series:Communications Biology
Online Access:https://doi.org/10.1038/s42003-025-08399-9
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author Mattia Utichi
Oana N. Antonescu
Valentina Sora
Henri-Baptiste Marjault
Matteo Tiberti
Emiliano Maiani
Matteo Lambrughi
Elena Papaleo
author_facet Mattia Utichi
Oana N. Antonescu
Valentina Sora
Henri-Baptiste Marjault
Matteo Tiberti
Emiliano Maiani
Matteo Lambrughi
Elena Papaleo
author_sort Mattia Utichi
collection DOAJ
description Abstract Short Linear Motifs (SLiMs) play a pivotal role in the interactions between intrinsically disordered proteins and their binding partners. SLiMs can undergo regulation through post-translational modifications, including phosphorylation. The flanking regions surrounding the core motifs also exert a crucial role for the interaction. While phosphorylation and flanking regions are known to influence SLiM function, the mechanistic basis of this regulation remains poorly understood. We integrate biomolecular simulations, in silico high-throughput mutational scans, and biophysical experiments to elucidate the phospho-regulation in SLiMs crucial for autophagy, i.e., the LC3 interacting regions (LIRs). We investigate the Optineurin LIR, which perfectly exemplifies a class of LIR with a complex interplay of phosphorylations and flanking regions. Here we show that specific phosphorylation events and flanking residues modulate binding to LC3 at the atomic level, and that disease-associated mutations alter these interactions in the phosphorylated context. Notably, we establish an approach based on Microfluidic Diffusional Sizing to investigate binding affinities of SLiMs to target proteins, complemented by Surface Plasmon Resonance, enabling precise measurements of dissociation constants and kinetics for a selection of variants. Our work provides a versatile toolkit to characterize phospho-regulated SLiMs, advancing the understanding of important cellular processes.
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spelling doaj-art-58892ec0492c443d9ebbe84d429cbeab2025-08-24T11:45:47ZengNature PortfolioCommunications Biology2399-36422025-08-018112010.1038/s42003-025-08399-9Decoding phospho-regulation and flanking regions in autophagy-associated short linear motifsMattia Utichi0Oana N. Antonescu1Valentina Sora2Henri-Baptiste Marjault3Matteo Tiberti4Emiliano Maiani5Matteo Lambrughi6Elena Papaleo7Cancer Structural Biology, Danish Cancer Institute, Strandboulevarden 49Cancer Structural Biology, Danish Cancer Institute, Strandboulevarden 49Cancer Structural Biology, Danish Cancer Institute, Strandboulevarden 49Cancer Structural Biology, Danish Cancer Institute, Strandboulevarden 49Cancer Structural Biology, Danish Cancer Institute, Strandboulevarden 49Cancer Structural Biology, Danish Cancer Institute, Strandboulevarden 49Cancer Structural Biology, Danish Cancer Institute, Strandboulevarden 49Cancer Structural Biology, Danish Cancer Institute, Strandboulevarden 49Abstract Short Linear Motifs (SLiMs) play a pivotal role in the interactions between intrinsically disordered proteins and their binding partners. SLiMs can undergo regulation through post-translational modifications, including phosphorylation. The flanking regions surrounding the core motifs also exert a crucial role for the interaction. While phosphorylation and flanking regions are known to influence SLiM function, the mechanistic basis of this regulation remains poorly understood. We integrate biomolecular simulations, in silico high-throughput mutational scans, and biophysical experiments to elucidate the phospho-regulation in SLiMs crucial for autophagy, i.e., the LC3 interacting regions (LIRs). We investigate the Optineurin LIR, which perfectly exemplifies a class of LIR with a complex interplay of phosphorylations and flanking regions. Here we show that specific phosphorylation events and flanking residues modulate binding to LC3 at the atomic level, and that disease-associated mutations alter these interactions in the phosphorylated context. Notably, we establish an approach based on Microfluidic Diffusional Sizing to investigate binding affinities of SLiMs to target proteins, complemented by Surface Plasmon Resonance, enabling precise measurements of dissociation constants and kinetics for a selection of variants. Our work provides a versatile toolkit to characterize phospho-regulated SLiMs, advancing the understanding of important cellular processes.https://doi.org/10.1038/s42003-025-08399-9
spellingShingle Mattia Utichi
Oana N. Antonescu
Valentina Sora
Henri-Baptiste Marjault
Matteo Tiberti
Emiliano Maiani
Matteo Lambrughi
Elena Papaleo
Decoding phospho-regulation and flanking regions in autophagy-associated short linear motifs
Communications Biology
title Decoding phospho-regulation and flanking regions in autophagy-associated short linear motifs
title_full Decoding phospho-regulation and flanking regions in autophagy-associated short linear motifs
title_fullStr Decoding phospho-regulation and flanking regions in autophagy-associated short linear motifs
title_full_unstemmed Decoding phospho-regulation and flanking regions in autophagy-associated short linear motifs
title_short Decoding phospho-regulation and flanking regions in autophagy-associated short linear motifs
title_sort decoding phospho regulation and flanking regions in autophagy associated short linear motifs
url https://doi.org/10.1038/s42003-025-08399-9
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