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A Screening Platform to Identify and Tailor Biocompatible Small-Molecule Catalysts.


ABSTRACT: Interfacing biocompatible, small-molecule catalysis with cellular metabolism promises a straightforward introduction of new function into organisms without the need for genetic manipulation. However, identifying and optimizing synthetic catalysts that perform new-to-nature transformations under conditions that support life is a cumbersome task. To enable the rapid discovery and fine-tuning of biocompatible catalysts, we describe a 96-well screening platform that couples the activity of synthetic catalysts to yield non-canonical amino acids from appropriate precursors with the subsequent incorporation of these nonstandard building blocks into GFP (quantifiable readout). Critically, this strategy does not only provide a common readout (fluorescence) for different reaction/catalyst combinations, but also informs on the organism's fitness, as stop codon suppression relies on all steps of the central dogma of molecular biology. To showcase our approach, we have applied it to the evaluation and optimization of transition-metal-catalyzed deprotection reactions.

SUBMITTER: Rubini R 

PROVIDER: S-EPMC6972700 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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A Screening Platform to Identify and Tailor Biocompatible Small-Molecule Catalysts.

Rubini Rudy R   Ivanov Ilya I   Mayer Clemens C  

Chemistry (Weinheim an der Bergstrasse, Germany) 20191118 70


Interfacing biocompatible, small-molecule catalysis with cellular metabolism promises a straightforward introduction of new function into organisms without the need for genetic manipulation. However, identifying and optimizing synthetic catalysts that perform new-to-nature transformations under conditions that support life is a cumbersome task. To enable the rapid discovery and fine-tuning of biocompatible catalysts, we describe a 96-well screening platform that couples the activity of synthetic  ...[more]

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