MoCHI: neural networks to fit interpretable models and quantify energies, energetic couplings, epistasis and allostery from deep mutational scanning data
MoCHI: нейронные сети для подгонки интерпретируемых моделей и количественной оценки энергий, энергетических взаимодействий, эпистаза и аллостерии по данным глубокого мутационного сканирования
2024-01-24
SCID: 54.1/dhy6vsau
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PyTorchallosteric mapsdeep mutational scanningenergetic couplingsepistasis
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Abstract (AI)
Abstract The massively parallel nature of deep mutational scanning (DMS) allows the quantification of the phenotypic effects of thousands of perturbations in a single experiment. We have developed MoCHI, a software tool that allows the parameterisation of arbitrarily complex models using DMS data. MoCHI simplifies the task of building custom models from measurements of mutant effects on any number of phenotypes. It allows the inference of free energy changes, as well as pairwise and higher-order interaction terms (energetic couplings) for specified biophysical models. When a suitable user-specified mechanistic model is not available, global nonlinearities (epistasis) can be estimated directly from the data. MoCHI also builds upon and leverages theory on ensemble (or background-averaged) epistasis to learn sparse predictive models that can incorporate higher-order epistatic terms and are informative of the genetic architecture of the underlying biological system. The combination of DMS and MoCHI allows biophysical measurements to be performed at scale, including the construction of complete allosteric maps of proteins. MoCHI is freely available ( https://github.com/lehner-lab/MoCHI ) and implemented as an easy-to-use python package relying on the PyTorch machine learning framework.
Key Findings
1
Combining DMS with MoCHI enables scalable biophysical measurements, including complete allosteric maps of proteins.
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MoCHI is a Python/PyTorch software tool for parameterizing arbitrarily complex, user-defined models from deep mutational scanning data.
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MoCHI uses ensemble epistasis theory to learn sparse predictive models containing higher-order terms that reveal underlying genetic architecture.
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The tool infers free-energy changes and pairwise or higher-order energetic couplings within specified biophysical models.
5
When no suitable mechanistic model exists, MoCHI estimates global nonlinearities and epistasis directly from experimental data.
Research Object
biological systems and proteins characterized by deep mutational scanning data
Research Subject
phenotypic effects, free-energy changes, energetic couplings, epistasis, and allosteric interactions inferred from mutational perturbations
Publication Details
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2024-01-24
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