Metal fluorides—multi-functional tools for the study of phosphoryl transfer enzymes, a practical guide

Enzymes facilitating the transfer of phosphate groups constitute the most extensive protein families across all kingdoms of life. They make up approximately 10% of the proteins found in the human genome. Understanding the mechanisms by which enzymes catalyze these reactions is essential in characterizing the processes they regulate. Metal fluorides can be used as multifunctional tools to study these enzymes. These ionic species bear the same charge as phosphate and the transferring phosphoryl group and, in addition, allow the enzyme to be trapped in catalytically important states with spectroscopically sensitive atoms interacting directly with active site residues. The ionic nature of these phosphate surrogates also allows their removal and replacement with other analogs. Here, we describe the best practices to obtain these complexes, their use in NMR, X-ray crystallography, cryo-EM, and SAXS and describe a new metal fluoride, scandium tetrafluoride, which has significant anomalous signal using soft X-rays.

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Publication Details

Journal
Structure
Published
2024-08-05
DOI
https://doi.org/10.1016/j.str.2024.07.007
Citations
3
Primary Topic
Enzyme Structure and Function
Type
article
Field-Weighted Citation Impact
0.35

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Metal fluorides—multi-functional tools for the study of phosphoryl transfer enzymes, a practical guide

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Metal fluorides—multi-functional tools for the study of phosphoryl transfer enzymes, a practical guide

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article en
3 citations

Abstract

Enzymes facilitating the transfer of phosphate groups constitute the most extensive protein families across all kingdoms of life. They make up approximately 10% of the proteins found in the human genome. Understanding the mechanisms by which enzymes catalyze these reactions is essential in characterizing the processes they regulate. Metal fluorides can be used as multifunctional tools to study these enzymes. These ionic species bear the same charge as phosphate and the transferring phosphoryl group and, in addition, allow the enzyme to be trapped in catalytically important states with spectroscopically sensitive atoms interacting directly with active site residues. The ionic nature of these phosphate surrogates also allows their removal and replacement with other analogs. Here, we describe the best practices to obtain these complexes, their use in NMR, X-ray crystallography, cryo-EM, and SAXS and describe a new metal fluoride, scandium tetrafluoride, which has significant anomalous signal using soft X-rays.

StructureVol. 32(10)
University of Manchester (GB), European Molecular Biology Laboratory (FR), University of Sheffield (GB)
Université Grenoble Alpes, European Molecular Biology Laboratory, French Infrastructure for Integrated Structural Biology, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 45%
Enzyme Structure and Function
0.35
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