There are many methods for introducing random mutations into nucleic acid sequences. Previously, we described a suite of programmes for estimating the completeness and diversity of randomized DNA libraries generated by a number of these protocols. Our programmes suggested some empirical guidelines for library design; however, no information was provided regarding library diversity at the protein (rather than DNA) level. We have now updated our web server, enabling analysis of translated libraries constructed by site-saturation mutagenesis and error-prone PCR (epPCR). We introduce GLUE-Including Translation (GLUE-IT), which finds the expected amino acid completeness of libraries in which up to six codons have been independently varied (accor...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
Directed molecular evolution and combinatorial methodologies are playing an increasingly important r...
The construction of custom libraries is critical for rational protein engineering and directed evolu...
A computer program for the generation and analysis of in silico random point mutagenesis libraries i...
During the last decade the use of randomised gene libraries has had an enormous impact in the field ...
Protein variant libraries produced by site-directed mutagenesis are a useful tool utilized by protei...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
AbstractThe laboratory evolution of functional proteins holds great fascination as an effective tool...
Site-directed mutagenesis and combinatorial libraries are powerful tools for providing information a...
We developed new criteria for determining the library size in a saturation mutagenesis experiment. W...
Genetic diversity creation is a core technology in directed evolution where a high quality mutant li...
Enzyme engineering allows to explore sequence diversity in search for new properties. The scientific...
Back in 2003, we published ‘MAX’ randomisation, a process of non-degenerate saturation mutagenesis u...
A directed evolution method has been developed that allows random substitution of a contiguous trinu...
The fraction of proteins that retain wild-type function after mutation has long been observed to dec...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
Directed molecular evolution and combinatorial methodologies are playing an increasingly important r...
The construction of custom libraries is critical for rational protein engineering and directed evolu...
A computer program for the generation and analysis of in silico random point mutagenesis libraries i...
During the last decade the use of randomised gene libraries has had an enormous impact in the field ...
Protein variant libraries produced by site-directed mutagenesis are a useful tool utilized by protei...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
AbstractThe laboratory evolution of functional proteins holds great fascination as an effective tool...
Site-directed mutagenesis and combinatorial libraries are powerful tools for providing information a...
We developed new criteria for determining the library size in a saturation mutagenesis experiment. W...
Genetic diversity creation is a core technology in directed evolution where a high quality mutant li...
Enzyme engineering allows to explore sequence diversity in search for new properties. The scientific...
Back in 2003, we published ‘MAX’ randomisation, a process of non-degenerate saturation mutagenesis u...
A directed evolution method has been developed that allows random substitution of a contiguous trinu...
The fraction of proteins that retain wild-type function after mutation has long been observed to dec...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
Directed molecular evolution and combinatorial methodologies are playing an increasingly important r...
The construction of custom libraries is critical for rational protein engineering and directed evolu...