In vitro synthesis of polypeptides by optimizing amino acid metabolism
View Patent ↗Compositions and methods are provided for the enhanced in vitro synthesis of polypeptides. In order to improve the performance of in vitro protein synthesis reactions, metabolic inhibitors, or manipulation of a source organism, is used to diminish or avoid the action of enzymes responsible for undesirable amino acids production or depletion. A homeostatic system may be used for production of ATP, where the required high energy phosphate bonds are generated in situ, e.g. through coupling with an oxidation reaction. The homeostatic energy source will typically lack high energy phosphate bonds itself, and will therefore utilize free phosphate in the reaction mix during generation of ATP. The homeostatic energy source is provided in combination with an enzyme that catalyzes the creation of high energy phosphate bonds and with an enzyme that can use that high energy phosphate bond to regenerate ATP.
1. A method for in vitro synthesis of polypeptides, the method comprising:
combining a template for polypeptide biosynthesis and a reaction mix comprising an E. coli extract deficient in the enzyme arginine decarboxylase.
2. A method for in vitro synthesis of polypeptides, the method comprising:
combining a template for polypeptide biosynthesis and a reaction mix comprising an E. coli extract deficient in the enzyme tryptophanase.
3. A method for in vitro synthesis of polypeptides, the method comprising:
combining a template for polypeptide biosynthesis and a reaction mix comprising an E. coli extract deficient in the enzyme alanine glutamate transaminase.
4. A method for in vitro synthesis of polypeptides, the method comprising:
combining a template for polypeptide biosynthesis and a reaction mix comprising an E. coli extract deficient in the enzyme E. coli pyruvate oxidase.
5. The method according to any of claims 1 to 4 wherein said E. coli extract is obtained by genetically inactivating said enzyme in said E. coli source of said extracts.
6. The method according to any of claims 1 to 4 wherein said E. coli extract is obtained by depleting said enzyme by affinity purification from said extract.