Degenerate codon (DC) libraries efficiently address the experimental library-size limitations of directed evolution by focusing diversity toward the positions and toward the amino acids (AAs) that are most likely to generate hits; however, manually constructing DC libraries is challenging, error prone and time consuming. This paper provides a dynamic programming solution to the task of finding the best DCs while keeping the size of the library beneath some given limit, improving on the existing integer-linear programming formulation. It then extends the algorithm to consider multiple DCs at each position, a heretofore unsolved problem, while adhering to a constraint on the number of primers needed to synthesize the library. In the two libra...
Efficient and economic methods in directed evolution at the protein, metabolic, and genome level are...
Efficient and economic methods in directed evolution at the protein, metabolic, and genome level are...
Back in 2003, we published ‘MAX’ randomisation, a process of non-degenerate saturation mutagenesis u...
Degenerate codon (DC) libraries efficiently address the experimental library-size limitations of dir...
Protein variant libraries produced by site-directed mutagenesis are a useful tool utilized by protei...
Degenerate codon libraries are frequently used in protein engineering and evolution studies but are ...
There are many methods for introducing random mutations into nucleic acid sequences. Previously, we ...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
Engineering proteins for designer functions and biotechnological applications almost invariably requ...
Saturation mutagenesis is employed in protein engineering and genome-editing efforts to generate lib...
DNA shuffling generates combinatorial libraries of chimeric genes by stochastically recombining pare...
Protein engineering can be performed by combinatorial techniques (directed evolution) and data-drive...
We have previously described ProxiMAX, a technology that enables the fabrication of precise, combina...
Protein engineering has been the most attractive strategy for biologists to redesign enzymes. As the...
Efficient and economic methods in directed evolution at the protein, metabolic, and genome level are...
Efficient and economic methods in directed evolution at the protein, metabolic, and genome level are...
Back in 2003, we published ‘MAX’ randomisation, a process of non-degenerate saturation mutagenesis u...
Degenerate codon (DC) libraries efficiently address the experimental library-size limitations of dir...
Protein variant libraries produced by site-directed mutagenesis are a useful tool utilized by protei...
Degenerate codon libraries are frequently used in protein engineering and evolution studies but are ...
There are many methods for introducing random mutations into nucleic acid sequences. Previously, we ...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
Engineering proteins for designer functions and biotechnological applications almost invariably requ...
Saturation mutagenesis is employed in protein engineering and genome-editing efforts to generate lib...
DNA shuffling generates combinatorial libraries of chimeric genes by stochastically recombining pare...
Protein engineering can be performed by combinatorial techniques (directed evolution) and data-drive...
We have previously described ProxiMAX, a technology that enables the fabrication of precise, combina...
Protein engineering has been the most attractive strategy for biologists to redesign enzymes. As the...
Efficient and economic methods in directed evolution at the protein, metabolic, and genome level are...
Efficient and economic methods in directed evolution at the protein, metabolic, and genome level are...
Back in 2003, we published ‘MAX’ randomisation, a process of non-degenerate saturation mutagenesis u...