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Engineering a Multifunctional Nitroreductase for Improved Activation of Prodrugs and PET Probes for Cancer Gene Therapy.

Cell Chem Biol. 2017; 
Copp JN, Mowday AM, Williams EM, Guise CP, Ashoorzadeh A, Sharrock AV, Flanagan JU, Smaill JB, Patterson AV, Ackerley DF.
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Codon Optimization Generation and Screening of a Combinatorial Library to Identify Improved NfsA Variants Based on the above results, a combinatorial gene library was generated (GenScript) to encode all 512 possible combinations of the 10 residue substitutions at the 8 identi?ed positions and the corresponding wild-type residues (Figure S1).... Combinatorial Library Construction Eight identi?ed positions (I5T, S41Y, E99G, L103M, K222E, R225x [x = A, G, P]), F227S, and L229V were chosen for inclusion in a synthetically constructed mutant gene library (GenScript; Figure S1), which, through the use of redun- dancy codons, was able to code for all possible 512 combinations of these mu- tations. Get A Quote

摘要

Gene-directed enzyme-prodrug therapy (GDEPT) is a?promising anti-cancer strategy. However, inadequate prodrugs, inefficient prodrug activation, and a lack of non-invasive imaging capabilities have hindered clinical progression. To address these issues, we used a high-throughput Escherichia coli platform to evolve the multifunctional nitroreductase E.?coli NfsA for improved activation of a promising next-generation prodrug, PR-104A, as well as clinically relevant nitro-masked positron emission tomography-imaging probes EF5 and HX4, thereby addressing a critical and unmet need for non-invasive bioimaging in nitroreductase GDEPT. The evolved variant performed better in E.?coli than in human cells, suggesting op... More

關鍵詞

BDEPT; GDEPT; PET imaging; PR-104A; SOS response; directed evolution; metabolic interference; nitroimidazole; nitroreductase; substrate promiscuity
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