Barbany, M.; Gutierrez-de-Teran, H.; Sanz, F.; Villà-Freixa...

来自 : www.oalib.com/references/8808. 发布时间：2021-03-25

ABSTRACT: Enzymes are tremendously proficient catalysts, which can be used as extracellular catalysts for a whole host of processes, from chemical synthesis to the generation of novel biofuels. For them to be more amenable to the needs of biotechnology, however, it is often necessary to be able to manipulate their physico-chemical properties in an efficient and streamlined manner, and, ideally, to be able to train them to catalyze completely new reactions. Recent years have seen an explosion of interest in different approaches to achieve this, both in the laboratory, and in silico. There remains, however, a gap between current approaches to computational enzyme design, which have primarily focused on the early stages of the design process, and laboratory evolution, which is an extremely powerful tool for enzyme redesign, but will always be limited by the vastness of sequence space combined with the low frequency for desirable mutations. This review discusses different approaches towards computational enzyme design and demonstrates how combining newly developed screening approaches that can rapidly predict potential mutation “hotspots” with approaches that can quantitatively and reliably dissect the catalytic step can bridge the gap that currently exists between computational enzyme design and laboratory evolution studies.
Barbany, M.; Gutierrez-de-Teran, H.; Sanz, F.; Villà-Freixa, J.; Warshel, A. On the generation of catalytic antibodies by transition state ...Barbany, M.; Gutierrez-de-Teran, H.; Sanz, F.; Villà-Freixa, J.; Warshel, A. On the generation of catalytic antibodies by transition state analogues. Chem Bio Chem 2003, 4, 277–285.Barbany, M.; Gutierrez-de-Teran, H.; Sanz, F.; Villà-Freixa, J.; Warshel, A. On the generation of catalytic antibodies by transition state analogues. Chem Bio Chem 2003, 4, 277–285.Barbany, M.; Gutierrez