Engineered thioredoxin-like fold proteins
The invention features compositions based on thioredoxin-like fold protein domains described as engineered thioredoxin-like fold proteins (ETRXs). These proteins include one or more artificially diversified thioredoxin-like fold protein domains; each domain may be originated from the same or different thioredoxin-like fold protein domains. Features of the invention also include methods for identifying and preparing an enriched composition of target binding, loop-diversified ETRXs with additional sequence variations to improve affinity, stability, selectivity, or solubility. The invention also features compositions of ETRXs substituted with prosthetic groups, polymers, proteins, nucleic acids, carbohydrates, metals, natural or synthetic small molecules and toxins.
1. A loop-diversified engineered human thioredoxin protein comprising a Cysteine to Serine mutation at C32 and C35, and at least one mutation in loop 1, loop 3, or loop 5, wherein the at least one mutation comprises at least one random amino acid(s) inserted between T30 and W31 in loop 1; or replacement of 5 residues between Ala69 and Pro75 with at least 5 randomized residues in loop 3.
2. The loop-diversified engineered human thioredoxin protein of claim 1 , which is derived from a protein comprising SEQ ID NO:219.
3. An undivided sample comprising a plurality of different loop-diversified engineered human thioredoxin proteins according to claim 1 .
4. The undivided sample of claim 3 comprising at least 100 distinct different loop-diversified engineered human thioredoxin proteins.
5. The loop-diversified engineered human thioredoxin protein of claim 1 , comprising SEQ ID NO:219 with a Cysteine to Serine mutation at C32 and C35 and mutations in loop 1 and loop 3.
6. The loop-diversified engineered human thioredoxin protein of claim 1 , comprising at least one of: one to nine random amino acids inserted between T30 and W31 in loop1; and replacement of 5 residues between Ala69 and Pro75 with 5 to 9 randomized residues in loop 3.
7. The loop-diversified engineered human thioredoxin protein of claim 6 , comprising a Cysteine to Serine mutation at C32 and C35, six random amino acids inserted between T30 and W31 in loop 1; and replacement of 5 residues between Ala69 and Pro75 with 9 randomized residues in loop 3.