Census of exposed aggregation-prone regions in proteomes
Authors:
- 17 May 2023
- journal article
- research article
- Published by Oxford University Press (OUP) in Briefings in Bioinformatics
- Vol. 24 (4)
Abstract
Loss of solubility usually leads to the detrimental elimination of protein function. In some cases, the protein aggregation is also required for beneficial functions. Given the duality of this phenomenon, it remains a fundamental question how natural selection controls the aggregation. The exponential growth of genomic sequence data and recent progress with in silico predictors of the aggregation allows approaching this problem by a large-scale bioinformatics analysis. Most of the aggregation-prone regions are hidden within the 3D structure, rendering them inaccessible for the intermolecular interactions responsible for aggregation. Thus, the most realistic census of the aggregation-prone regions requires crossing aggregation prediction with information about the location of the natively unfolded regions. This allows us to detect so-called ‘exposed aggregation-prone regions’ (EARs). Here, we analyzed the occurrence and distribution of the EARs in 76 reference proteomes from the three kingdoms of life. For this purpose, we used a bioinformatics pipeline, which provides a consensual result based on several predictors of aggregation. Our analysis revealed a number of new statistically significant correlations about the presence of EARs in different organisms, their dependence on protein length, cellular localizations, co-occurrence with short linear motifs and the level of protein expression. We also obtained a list of proteins with the conserved aggregation-prone sequences for further experimental tests. Insights gained from this work led to a deeper understanding of the relationship between protein evolution and aggregation.Keywords
All Related Versions
Funding Information
- Latin America in Research and Innovation Staff Exchange Program (H2020-MSCA-RISE-2018)
- Azerbaijan National Academy of Sciences
- Ministry of Science and Education of Azerbaijan
- Ministère de l’Education Nationale de la Recherche et de Technologie
This publication has 60 references indexed in Scilit:
- Prediction of the aggregation propensity of proteins from the primary sequence: Aggregation properties of proteomesBiotechnology Journal, 2011
- Protein Aggregation Profile of the Bacterial CytosolPLOS ONE, 2010
- Identifying the amylome, proteins capable of forming amyloid-like fibrilsProceedings of the National Academy of Sciences, 2010
- Aggregation Propensity of the Human ProteomePLOS Computational Biology, 2008
- Natural Selection against Protein Aggregation on Self-Interacting and Essential Proteins in Yeast, Fly, and WormMolecular Biology and Evolution, 2008
- The Zyggregator method for predicting protein aggregation propensitiesChemical Society Reviews, 2008
- AGGRESCAN: a server for the prediction and evaluation of "hot spots" of aggregation in polypeptidesBMC Bioinformatics, 2007
- Curli Biogenesis and FunctionAnnual Review of Microbiology, 2006
- Prediction of sequence-dependent and mutational effects on the aggregation of peptides and proteinsNature Biotechnology, 2004
- Predicting transmembrane protein topology with a hidden markov model: application to complete genomes11Edited by F. CohenJournal of Molecular Biology, 2001