| Home > Articles > Published articles > AGGRESCAN and its evolution : |
| Date: | 2026 |
| Abstract: | Protein aggregation is a widespread phenomenon with profound biological, biomedical, and biotechnological implications. In human disease, aberrant protein self-assembly is a hallmark of numerous neurodegenerative disorders, whereas in the biopharmaceutical industry, aggregation complicates the production, stability, and formulation of therapeutic proteins. The Aggrescan platform was one of the first empirically based tools designed to predict aggregation-prone regions (APRs) within protein sequences. It has since expanded to incorporate three-dimensional structural contexts and environmental conditions. This review provides a comprehensive overview of the development, application, and impact of the Aggrescan family of tools, which includes AGGRESCAN, Aggrescan3D, and the recent Aggrescan4D. We examine the algorithmic foundations, empirical validation, and key use cases spanning fields from biotechnology to biomedical research. Additionally, we describe how the recent integration of AlphaFold models has enabled proteome-scale exploration of aggregation determinants. This review highlights how Aggrescan has evolved alongside with advances in the field, becoming a reliable and accessible tool for studying and redesigning protein aggregation. |
| Grants: | Agencia Estatal de Investigación PID2022-137963OB-I00 Generalitat de Catalunya 2021/SGR-00635 Ministerio de Ciencia, Innovación y Universidades FPU22/03656 |
| Note: | Altres ajuts: acords transformatius de la UAB |
| Rights: | Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. |
| Language: | Anglès |
| Document: | Article de revisió ; recerca ; Versió publicada |
| Subject: | Protein aggregation ; Aggregation-prone regions ; Computational protein design ; Amyloid ; Molecular dynamics ; Protein therapeutics |
| Published in: | Biophysical Reviews, January 2026, ISSN 1867-2469 |
12 p, 3.4 MB |