Abstract 2343 Functional Characterization and Inhibitor Screening of the Monotopic Phosphoglycosyl Transferase Superfamily Using a Novel Protein-Purification-Free Approach for Antibiotic Drug Discovery
The rise of antibiotic resistance has intensified the need for new bacterial targets for therapeutic intervention. Monotopic phosphoglycosyl transferases (monoPGTs), a class of exclusively prokaryotic membrane proteins that remain poorly understood, represent promising targets for pharmacological intervention against human pathogens, including Campylobacter jejuni and Streptococcus pneumoniae. MonoPGTs play a key role in glycoconjugate synthesis, which is crucial for bacterial pathogenesis. These enzymes initiate glycan biosynthesis by transferring a sugar-phosphate from a soluble nucleotide diphosphate sugar to a polyprenol phosphate acceptor in the membrane.
Authors
- Hugh Higinbotham (ORCID: https://orcid.org/0000-0002-9418-7958)
- Barbara Imperiali (ORCID: https://orcid.org/0000-0002-5749-7869)
- Karen N. Allen (ORCID: https://orcid.org/0000-0001-7296-0551)
- Christine A. Arbour (ORCID: https://orcid.org/0000-0001-6056-296X)
- Greg J. Dodge (ORCID: https://orcid.org/0000-0002-6555-8350)
- Soumi Ghosh (ORCID: https://orcid.org/0000-0001-6101-0147)
- Theo Durand (ORCID: https://orcid.org/0009-0004-8131-581X)
- Roxanne P. Siuda (ORCID: https://orcid.org/0000-0001-7387-8429)
Institutions
- Boston Medical Center (US)
Publication Details
- Journal
- Journal of Biological Chemistry
- Published
- 2025-05-01
- DOI
- https://doi.org/10.1016/j.jbc.2025.109337
- Primary Topic
- Carbohydrate Chemistry and Synthesis
- Type
- article
- Field-Weighted Citation Impact
- 0.00