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Automated optimization of the solubility of a hyper-stable α-amylase

Open Biol. 2024-05; 
Montader Ali, Matthew Greenig, Marc Oeller, Misha Atkinson, Xing Xu, Pietro Sormanni
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Proteins, Expression, Isolation and Analysis … PBS and loaded onto the GenScript AmMag SA Plus purification system (GenScript, cat. … protein was eluted and collected in PBS fractions with 40- and 200 mM Imidazole. The proteins … Get A Quote

摘要

Most successes in computational protein engineering to date have focused on enhancing one biophysical trait, while multi-trait optimization remains a challenge. Different biophysical properties are often conflicting, as mutations that improve one tend to worsen the others. In this study, we explored the potential of an automated computational design strategy, called CamSol Combination, to optimize solubility and stability of enzymes without affecting their activity. Specifically, we focus on α-amylase (BLA), a hyper-stable enzyme that finds diverse application in industry and biotechnology. We validate the computational predictions by producing 10 BLA variants, including the wild-type (WT) and three designed ... More

關鍵詞

enzyme optimization, protein design, protein solubility
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