Large-scale protein production for biotechnology and biopharmaceutical applications rely on high protein solubility in expression systems. Solubility has been measured for a significant fraction of E. coli and S. cerevisiae proteomes and these datasets are routinely used to train predictors of protein solubility in different organisms. Thanks to continued advances in experimental structure-determination and modelling, many of these solubility measurements can now be paired with accurate structural models.
The challenge is mentored by Christopher Ing and Mark Fingerhuth.
It is the objective of this project to use our provided dataset of protein structure and solubility value pairs in order to produce a solubility predictor with comparable accuracy to sequence-based predictors reported in the literature. The provided dataset to be used in this project is created by following the dataset curation procedure described in the SOLart paper, and this hackathon project has a similar aim to this manuscript.
The process of generating the dataset is described in the SOLArt manuscript. At a high level, all experimentally tested E. coli and S. cerevisiae proteins were matched through Uniprot IDs to known crystallographic structures or high sequence similarity homology models. After balancing the fold types using CATH, a dataset containing a balanced spread of solubility values was produced. The resulting proteins for the training and testing of these models were prepared and disclosed in the supplemental material of this paper as a list of (Uniprot,PDB,Chain,Solubility) pairs. The PDB files were not included in this work so we had to re-extract them from SWISS-MODEL. Whenever a crystallographic structure was present, it was used, assuming high coverage over the Uniprot sequence. In some cases, the original PDB templates used within the original SOLArt paper had been superceded by improved templates, and we opted to take the highest resolution, highest sequence identity, models in our updated dataset. We stripped away all irrelevant chains and heteroatoms.
If issues are identified with individual structures, please refer to the Uniprot ID and manually investigate the best template. In some cases, we needed to improve structure correctness by modelling missing atoms/residues inside the Chemical Computing Group software MOE on a case-by-case basis.
Your code should output a file called predictions.csv in the following format:
protein,solubility
P69829,83
P31133,62
whereby the protein column contains the Uniprot ID (corresponds to the filename of the PDB files) and the solubility column contains the predicted solubility value (can be int or float).
Note, that there are three (!) test subsets but you are expected to submit all the predictions in one file (not three) for the benchmarking system to work.
The continuous integration script in .github/workflows/ci.yml will automatically build the Dockerfile on every commit to the main branch. This docker image will be published as your hackathon submission to https://biolib.com/<YourTeam>/<TeamName>. For this to work, make sure you set the BIOLIB_TOKEN and BIOLIB_PROJECT_URI accordingly as repository secrets.
To read more about the benchmarking system click here.
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