DNA shuffling of a family of genes from diverse species accelerates directed evolution
By A. Crameri, S. Raillard, Ericka Bermudez, W. Stemmer. 1998
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Citations in the corpus
- Exploring protein fitness landscapes by directed evolution (2009, positive): “Naturally-occurring homologous proteins can be recombined to create genetic diversity within protein sequence librarie”
- Directed Polymerase Evolution (2013, methodology): “Family shuffling has proven to be an effective way to construct high-quality libraries; however, reassembly is relatively inefficient when the method is applied to regions with low sequence homology [45].”
- Programming cells by multiplex genome engineering and accelerated evolution (2009, background): “7); (2) induce cells for allelic replacement via 42 uC heat shock for 15 min; (3) chill cells at 4 uC to halt cellular metabolism; (4) wash cells through 15–20 iterations of filtration and resuspension with dH2O; (5) mix cell suspension and synthetic DNA; (6) deliver DNA into cells by electroporatio”
- Golden Gate Shuffling: A One-Pot DNA Shuffling Method Based on Type IIs Restriction Enzymes (2009, background): “For example, libraries can be constructed from pools of DNaseI digested fragments prepared from parental templates [5,6,7,8], from degenerate oligonucleotides [9,10] or from mixtures of both, or even from undigested parental templates [11,12,13], and are usually assembled through PCR.”
- Directed evolution of new catalytic activity using the α/β-barrel scaffold (2000, background): “, the generation of mutants must be coupled to a suitable selection procedure to allow in vitro evolutio”
- PERSPECTIVE: TRANSPOSABLE ELEMENTS, PARASITIC DNA, AND GENOME EVOLUTION (2001, background): “Experimental evolution (Moore et al. 1997; Zhang et al. 1997; Crameri et al. 1998) and computer simulation experiments (Bogarad and Deem 1999) showed that sequence shuffling has the potential to improve protein function significantly better than does point mutation alone.”
- Improving catalytic function by ProSAR-driven enzyme evolution (2007, methodology): “The iterative nature of this approach results in stepwise improvements in overall function, yielding substantial improvements in desired enzyme propertie”
- In silico protein design by combinatorial assembly of protein building blocks (2004, methodology): “Recombination is a powerful tool for the engineering and optimization of proteins in vitro (Crameri et al. 1998; Riechmann and Winter 2000).”
- Protein building blocks preserved by recombination (2002, background): “It promotes the combination of traits from multiple parents onto a single offspring, thus exploiting information obtained in previous rounds of selectio”
- Adeno-associated virus serotypes: vector toolkit for human gene therapy. (2006, background): “Template switching causes crossovers in areas of sequence homology [117].”