Aggrescan3D (A3D) 2.0

Protein aggregation is a hallmark of a growing number of human disorders and constitutes a major bottleneck in the manufacturing of therapeutic proteins. Therefore, there is a strong need of in-silico methods that can anticipate the aggregative properties of protein variants linked to disease and as...

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Detalles Bibliográficos
Autores: Kuriata, Aleksander, Iglesias, Valentin|||0000-0002-6133-0869, Pujols Pujol, Jordi|||0000-0001-9424-5866, Kurcinski, Mateusz, Kmiecik, Sebastian|||0000-0001-7623-0935, Ventura, Salvador|||0000-0002-9652-6351
Tipo de recurso: artículo
Fecha de publicación:2019
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:222827
Acceso en línea:https://ddd.uab.cat/record/222827
https://dx.doi.org/urn:doi:10.1093/nar/gkz321
Access Level:acceso abierto
Palabra clave:Algorithms
Humans
Information dissemination
Internet
Protein aggregates
Protein aggregation, pathological
Protein multimerization
Protein stability
Proteins
Software
Solubility
Descripción
Sumario:Protein aggregation is a hallmark of a growing number of human disorders and constitutes a major bottleneck in the manufacturing of therapeutic proteins. Therefore, there is a strong need of in-silico methods that can anticipate the aggregative properties of protein variants linked to disease and assist the engineering of soluble protein-based drugs. A few years ago, we developed a method for structure-based prediction of aggregation properties that takes into account the dynamic fluctuations of proteins. The method has been made available as the Aggrescan3D (A3D) web server and applied in numerous studies of protein structure-aggregation relationship. Here, we present a major update of the A3D web server to version 2.0. The new features include: extension of dynamic calculations to significantly larger and multimeric proteins, simultaneous prediction of changes in protein solubility and stability upon mutation, rapid screening for functional protein variants with improved solubility, a REST-ful service to incorporate A3D calculations in automatic pipelines, and a new, enhanced web server interface. A3D 2.0 is freely available at: http://biocomp.chem.uw.edu.pl/A3D2/.