Biology subjects

Abakarova, M.

Publications and source records attributed to Abakarova, M..

3 recordsLinked to original sources

bioRxiv2025

Proteome-wide prediction of the Functional Impact of Missense Variants with ProteoCast

Dissecting the functional impact of genetic mutations is essential to advancing our understanding of genotype-phenotype relationships and identifying therapeutic targets. Despite progress in sequencing and genome editing technologies, proteome-wide mutation effect prediction remains challenging. Here we show that evolutionary information alone enables accurate prediction of mutation effects across entire proteomes. ProteoCast is a scalable and interpretable computational method that leverages protein sequence conservation to classify genetic variants and identify functionally important protein sites. We apply ProteoCast to the complete Drosophila melanogaster proteome (22,000 isoforms, 300 million mutations) and validate it against nearly 400,000 natural and experimental variants. It correctly classifies 85% of known lethal mutations as functionally impactful versus 13-18% of population variants. ProteoCast-guided genome editing experiments confirm these predictions. Moreover, ProteoCast successfully identifies functionally important protein modification sites and binding motifs. ProteoCast provides a publicly available resource and deployable pipeline for studying gene function and mutations in any organism.

evolutionary biology↗

bioRxiv2024

VespaG: Expert-guided protein Language Models enable accurate and blazingly fast fitness prediction

Exhaustive experimental annotation of the effect of all known protein variants remains daunting and expensive, stressing the need for scalable effect predictions. We introduce VespaG, a blazingly fast missense amino acid variant effect predictor, leveraging protein Language Model (pLM) embeddings as input to a minimal deep learning model. To overcome the sparsity of experimental training data, we created a dataset of 39 million single amino acid variants from the human proteome applying the multiple sequence alignment-based effect predictor GEMME as a pseudo standard-of-truth. This setup increases interpretability compared to the baseline pLM and is easily retrainable with novel or updated pLMs. Assessed against the ProteinGym benchmark (217 multiplex assays of variant effect - MAVE - with 2.5 million variants), VespaG achieved a mean Spearman correlation of 0.48{+/-}0.02, matching top-performing methods evaluated on the same data. VespaG has the advantage of being orders of magnitude faster, predicting all mutational landscapes of all proteins in proteomes such as Homo sapiens or Drosophila melanogaster in under 30 minutes on a consumer laptop (12-core CPU, 16 GB RAM). AvailabilityVespaG is available freely at https://github.com/jschlensok/vespag. The associated training data and predictions are available at https://doi.org/10.5281/zenodo.11085958.

bioinformatics↗

bioRxiv2022

Alignment-based protein mutational landscape prediction: doing more with less

The wealth of genomic data has boosted the development of computational methods predicting the phenotypic outcomes of missense variants. The most accurate ones exploit multiple sequence alignments, which can be costly to generate. Recent efforts for democratizing protein structure prediction have overcome this bottleneck by leveraging the fast homology search of MMseqs2. Here, we show the usefulness of this strategy for mutational outcome prediction through a large-scale assessment of 1.5M missense variants across 72 protein families. Our study demonstrates the feasibility of producing alignment-based mutational landscape predictions that are both high-quality and compute-efficient for entire proteomes. We provide the community with the whole human proteome mutational landscape and simplified access to our predictive pipeline. Significant statementUnderstanding the implications of DNA alterations, particularly missense variants, on our health is paramount. This study introduces a faster and more efficient approach to predict these effects, harnessing vast genomic data resources. The speed-up is possible by establishing that resource-saving multiple sequence alignments suffice even as input to a method fitting few parameters given the alignment. Our results opens the door to discovering how tiny changes in our genes can impact our health. They provide valuable insights into the genotype-phenotype relationship that could lead to new treatments for genetic diseases.

bioinformatics↗