Computational optimization of cell culture media for cultured meat production

One of the biggest challenges in making cultured meat accessible is reducing the cost of culture media. This project outlines two methods of reducing cost of media: 1) optimisation of concentration of components and 2) discovery of alternative components. Optimisation of culture media components wa...

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Bibliographic Details
Main Author: Reji, Rinta Pullamkottu
Other Authors: -
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2023
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Online Access:https://hdl.handle.net/10356/166433
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Institution: Nanyang Technological University
Language: English
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Summary:One of the biggest challenges in making cultured meat accessible is reducing the cost of culture media. This project outlines two methods of reducing cost of media: 1) optimisation of concentration of components and 2) discovery of alternative components. Optimisation of culture media components was modelled as a blackbox optimisation problem with test functions to replace in vitro optimisation. A comparison of algorithmic methods for media optimisation was done at low, medium and high dimension and found that the best performing method was surrogate-based optimisation with truncated differential evolution as the acquisition method. This method is currently under-utilised and thus could improve media optimisation. Protein hydrolysates are viable substitutes for serum in culture media. To classify potentially useful hydrolysates, a structure-based prediction graph convolutional network (GCN) was trained on predicted structural information from AlphaFold2. ESM-2 was trained on amino acid sequences for masked residue prediction in order to extract residue-level features to be embedded into the graphical input. Even though the GCN (without residue-level features) did not perform the classification task well, ESM-2 was able to achieve a phenomenal performance with ROC-AUC of 0.94. ESM-2 is deep enough to capture protein function and can be used to classify serum-equivalent hydrolysates.