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Giannakoulias, S.

Publications and source records attributed to Giannakoulias, S..

3 recordsLinked to original sources

Proteins Need Extra Attention: Improving the Predictive Power of Protein Language Models on Mutational Datasets with Hint Tokens

In this computational study, we introduce "hint token learning," a novel machine learning approach designed to enhance protein language modeling. This method effectively addresses the unique challenges of protein mutational datasets, characterized by highly similar inputs that may differ by only a single token. Our research highlights the superiority of hint token learning over traditional fine-tuning methods through three distinct case studies. We first developed a highly accurate free energy of folding model using the largest protein stability dataset to date. Then, we applied hint token learning to predict a biophysical attribute, the brightness of green fluorescent protein mutants. In our third case, hint token learning was utilized to assess the impact of mutations on RecA bioactivity. These diverse applications collectively demonstrate the potential of hint token learning for improving protein language modeling across general and specific mutational datasets. To facilitate broader use, we have integrated our protein language models into the HuggingFace ecosystem for downstream, mutational fine-tuning tasks.

bioinformatics↗

Prot-SCL: State Of The Art Prediction Of Protein Subcellular Localization From Primary Sequence Using Contrastive Learning

Protein subcellular localization is a critically important parameter to consider when designing expression constructs and production strategies for industry scale protein production. In this study, we present Prot-SCL an innovative self-supervised machine learning approach to predict protein subcellular localization exclusively from primary sequence. The models herein were learned from a dataset of subcellular localizations derived by exhaustively analyzing the Uniprot database. The set of localization data was rigorously curated for machine learning by employing group sampling following clustering of the protein sequences. The novel component of this approach lies in the development of a triplet neural network architecture capable of generating meaningful embeddings for classification of protein subcellular localization. We observed a robust predictive power for our classical gradient boosted machine learning models trained on these triplet embeddings in both cross validation and in generalization to the testing set. Importantly, we have made this extensive dataset of protein subcellular localizations publicly accessible, facilitating future, need-based, localization studies. Finally, we provide the relevant codebase to encourage a wider adoption and expansion of this methodology. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=123 SRC="FIGDIR/small/555932v1_ufig1.gif" ALT="Figure 1"> View larger version (52K): org.highwire.dtl.DTLVardef@1d9b205org.highwire.dtl.DTLVardef@1368c23org.highwire.dtl.DTLVardef@2a88edorg.highwire.dtl.DTLVardef@8380b7_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioinformatics↗

Rosetta Custom Score Functions Accurately Predict ΔΔG of Mutations at Protein-Protein Interfaces Using Machine Learning

Protein-protein interfaces play essential roles in a variety of biological processes and many therapeutic molecules are targeted at these interfaces. However, accurate predictions of the effects of interfacial mutations to identify "hotspots" have remained elusive despite the myriad of modeling and machine learning methods tested. Here, for the first time, we demonstrate that nonlinear reweighting of energy terms from Rosetta, through the use of machine learning, exhibits improved predictability of {Delta}{Delta}G values associated with interfacial mutations.

biophysics↗