ArticleBMC bioinformatics2014
A review of machine learning methods to predict the solubility of overexpressed recombinant proteins in Escherichia coli.
Article in BMC bioinformatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.
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Who cites it
25 citing papers in PubMed, 68 citations in OpenAlex.
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- Protein Extraction and Purification by Differential Solubilization.Methods in molecular biology (Clifton, N.J.) · 2023Article
- Protein Design: From the Aspect of Water Solubility and Stability.Chemical reviews · 2022Review
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- Artificial Intelligence, Machine Learning and Deep Learning in Ion Channel Bioinformatics.Membranes · 2021Review
- Platforms for Production of Protein-Based Vaccines: From Classical to Next-Generation Strategies.Biomolecules · 2021Review
- Solubility and Aggregation of Selected Proteins Interpreted on the Basis of Hydrophobicity Distribution.International journal of molecular sciences · 2021Article
- Structure-aware protein solubility prediction from sequence through graph convolutional network and predicted contact map.Journal of cheminformatics · 2021Article
- Solubility-Weighted Index: fast and accurate prediction of protein solubility.Bioinformatics (Oxford, England) · 2020Article
- Solubility of proteins.ADMET & DMPK · 2020Article
- A guide to machine learning for bacterial host attribution using genome sequence data.Microbial genomics · 2019Article
- Establishing synthesis pathway-host compatibility via enzyme solubility.Biotechnology and bioengineering · 2019Article
- Codon usage clusters correlation: towards protein solubility prediction in heterologous expression systems in E. coli.Scientific reports · 2018Article
- Correlation Between Protein Primary Structure and Soluble Expression Level of HSA dAb inFood technology and biotechnology · 2018Article
- Machine learning to design integral membrane channelrhodopsins for efficient eukaryotic expression and plasma membrane localization.PLoS computational biology · 2017Article
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundOver the last 20 years in biotechnology, the production of recombinant proteins has been a crucial bioprocess in both biopharmaceutical and research arena in terms of human health, scientific impact and economic volume. Although logical strategies of genetic engineering have been established, protein overexpression is still an art. In particular, heterologous expression is often hindered by low level of production and frequent fail due to opaque reasons. The problem is accentuated because there is no generic solution available to enhance heterologous overexpression. For a given protein, the extent of its solubility can indicate the quality of its function. Over 30% of synthesized proteins are not soluble. In certain experimental circumstances, including temperature, expression host, etc., protein solubility is a feature eventually defined by its sequence. Until now, numerous methods based on machine learning are proposed to predict the solubility of protein merely from its amino acid sequence. In spite of the 20 years of research on the matter, no comprehensive review is available on the published methods.
resultsThis paper presents an extensive review of the existing models to predict protein solubility in Escherichia coli recombinant protein overexpression system. The models are investigated and compared regarding the datasets used, features, feature selection methods, machine learning techniques and accuracy of prediction. A discussion on the models is provided at the end.
conclusionsThis study aims to investigate extensively the machine learning based methods to predict recombinant protein solubility, so as to offer a general as well as a detailed understanding for researches in the field. Some of the models present acceptable prediction performances and convenient user interfaces. These models can be considered as valuable tools to predict recombinant protein overexpression results before performing real laboratory experiments, thus saving labour, time and cost.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.