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Biology subjects

Reuel, N.

Publications and source records attributed to Reuel, N..

2 recordsLinked to original sources

Improved Functional Classification of Hydrolases through Pairwise Structural Similarity of Reaction Cores

We report a systematic pipeline is for extracting the catalytically relevant reactive site in addition to the surrounding allosterically linked residue shells around the reaction site of the most diverse enzyme class - hydrolases, with known experimental structures. We first successfully extract 40196 such hydrolase reaction cores (RC) and collates them into a publicly accessible reaction core collection (RC-Hydrolase). We perform 128M pairwise shape comparison across RC-Hydrolase using a three-dimensional search engine and present 155,329 pair instances clustering them by 60% or higher similarities in a publicly available, visually interactive dataset. Robustness of defined RCs is shown to successfully capture experimentally known function-enhancing mutations distal to the active site in PETases. Allowing comparisons of enzyme reaction centers across functional spaces (ligands bound, EC classification numbers, and expression hosts) enables identification of enzyme backbones which can be minimally mutated to accommodate more than one type of catalytic activity thereby aiding rational design of multifunctional enzymes. We also demonstrate how such versatile enzyme backbones could be leveraged by the latest diffusion-based protein design models to design bespoke libraries of small molecule inhibitors, and structurally stable multifunctional enzyme pockets. With only sporadic successes in multifunctional enzyme design thus far, we provide strong structural priors for machine-learning-guided advanced enzyme engineering in the future.

bioinformatics↗

Controlling Heterogeneity and Increasing Titer from Riboswitch-Regulated Bacillus subtilis Spores for Time-Delayed Protein Expression Applications

Sporulated cells have potential as time-delayed expression chassis of proteins for applications such as on-demand biologics production, whole cell biosensors, or oral vaccines. However, the desired attributes of high expression rates and low product variances are difficult to maintain from germinated spores. In this work we study the effect of an integrating vs. theta replicating plasmid in a wild-type Bacillus subtilis and two PolY mutants. The cells were engineered to produce a fluorescent reporter protein (RFP) under the control of a riboswitch activated by theophylline. This allowed for greater sensitivity to point mutations. The fluorescence and cell growth curves were fit with a custom kinetic model and a peak kinetic rate (LKPmax) was extracted for each clonal population (n = 30 for all cell, vector, and growth combinations). Plasmid based expression yields higher (8.7x) expression rates due to an increased copy number of the expression cassette (10x over integrated). The variance of LKPmax values increased 2.07x after sporulation for the wild type strain. This increase in variance from sporulation is very similar to what is observed with UV exposure. This effect can be partially mitigated by the use of PolY knockouts observed in suspended cell growths and adherent biofilms.

microbiology↗