Publications by authors named "J S Finnigan"

Glycan-mediated interactions play a crucial role in biology and medicine, influencing signalling, immune responses, and disease pathogenesis. However, the use of glycans in biosensing and diagnostics is limited by cross-reactivity, as certain glycan motifs can be recognised by multiple biologically distinct protein receptors. To address this specificity challenge, we report the enzymatic synthesis of a 150-member library of site-specifically fluorinated Lewis analogues ('glycofluoroforms') using naturally occurring enzymes and fluorinated monosaccharides.

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In the ever-growing demand for sustainable ways to produce high-value small molecules, biocatalysis has come to the forefront of greener routes to these chemicals. As such, the need to constantly find and optimise suitable biocatalysts for specific transformations has never been greater. Metagenome mining has been shown to rapidly expand the toolkit of promiscuous enzymes needed for new transformations, without requiring protein engineering steps.

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  • T cell receptors (TCR) play a crucial role in identifying and attacking tumor cells by recognizing unique neoantigens produced from mutations, but the details on how TCRs recognize these neoantigens are still unclear.
  • This study focuses on a specific neoantigen from B16F10 murine melanoma and its corresponding TCR, showing that a particular mutation improves the binding to MHC-I, enhancing the presentation on cell surfaces.
  • The TCR studied demonstrated strong binding and recognition capabilities, even in low antigen situations, highlighting the importance of molecular studies for understanding how neoantigens induce immune responses against cancer.
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  • * Two engineered FMN-dependent "ene"-reductases (EREDs) were developed to enable regiodivergent hydroalkylations, allowing for easier creation of constitutional isomers compared to traditional methods.
  • * Specific engineered variants of EREDs were designed to favor different unsaturated ketones during the reaction, with accompanying investigations into the effects of mutations and the mechanism using isotope labeling.
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Enzymes are being increasingly exploited for their potential as industrial biocatalysts. Establishing a portfolio of useful biocatalysts from large and diverse protein family is challenging and a systematic method for candidate selection promises to aid in this task. Moreover, accurate enzyme functional annotation can only be confidently guaranteed through experimental characterisation in the laboratory.

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