Comprehensive protein datasets and benchmarking for liquid-liquid phase separation studies
Pintado-Grima, Carlos (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular)
Bárcenas, Oriol (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular)
Arribas-Ruiz, Eva (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular)
Iglesias, Valentin (Medical University of Białystok)
Burdukiewicz, Michał (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular)
Ventura, Salvador (Parc Taulí Hospital Universitari. Institut d'Investigació i Innovació Parc Taulí (I3PT))

Fecha:	2025
Resumen:	Proteins self-organize in dynamic cellular environments by assembling into reversible biomolecular condensates through liquid-liquid phase separation (LLPS). These condensates can comprise single or multiple proteins, with different roles in the ensemble's structural and functional integrity. Driver proteins form condensates autonomously, while client proteins just localize within them. Although several databases exist to catalog proteins undergoing LLPS, they often contain divergent data that impedes interoperability between these resources. Additionally, there is a lack of consensus on selecting proteins without explicit experimental association with condensates under physiological conditions (non-LLPS proteins or negative proteins). These two aspects have prevented the generation of reliable predictive models and fair benchmarks. In this work, we use an integrated biocuration protocol to analyze information from all relevant LLPS databases and generate confident datasets of client and driver proteins. We introduce standardized negative datasets, encompassing both globular and disordered proteins. To validate our datasets, we investigate specific physicochemical traits related to LLPS across different subsets of protein sequences and benchmark them against 16 predictive algorithms. We observe significant differences not only between positive and negative instances but also among LLPS proteins themselves. The datasets from this study are available as a website at and as a data repository at . Our datasets offer a reliable means for confidently assessing the specific roles of proteins in LLPS and identifying key differences in physicochemical properties underlying this process. Moreover, we describe limitations in classical and state-of-the-art predictive algorithms by providing the most comprehensive benchmark to date. {'@id': 'Par4', 'graphic': {'@position': 'anchor', '@id': 'MO1', '@orientation': 'portrait', '@xlink:href': '13059_2025_3668_Figa_HTML. jpg'}} The online version contains supplementary material available at 10. 1186/s13059-025-03668-6.
Ayudas:	Agencia Estatal de Investigación PID2022-137963OB-I00 Generalitat de Catalunya 2021-SGR-00635
Derechos:	Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades.
Lengua:	Anglès
Documento:	Article ; recerca ; Versió publicada
Materia:	Liquid-liquid phase separation ; Datasets ; Integration ; Driver ; Client ; Negative ; Proteins ; Disorder ; Machine learning ; Benchmark
Publicado en:	Genome biology, Vol. 26 (July 2025) , art. 198, ISSN 1474-760X

DOI: 10.1186/s13059-025-03668-6
PMID: 40629388

21 p, 3.3 MB

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Documentos de investigación > Documentos de los grupos de investigación de la UAB > Centros y grupos de investigación (producción científica) > Ciencias de la salud y biociencias > Instituto de Investigación e Innovación Parc Taulí (I3PT)
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