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Structures of trehalose-6-phosphate synthase, Tps1, from the fungal pathogen Cryptococcus neoformans: A target for antifungals.

Publication ,  Journal Article
Washington, EJ; Zhou, Y; Hsu, AL; Petrovich, M; Tenor, JL; Toffaletti, DL; Guan, Z; Perfect, JR; Borgnia, MJ; Bartesaghi, A; Brennan, RG
Published in: Proc Natl Acad Sci U S A
August 6, 2024

Invasive fungal diseases are a major threat to human health, resulting in more than 1.5 million annual deaths worldwide. The arsenal of antifungal therapeutics remains limited and is in dire need of drugs that target additional biosynthetic pathways that are absent from humans. One such pathway involves the biosynthesis of trehalose. Trehalose is a disaccharide that is required for pathogenic fungi to survive in their human hosts. In the first step of trehalose biosynthesis, trehalose-6-phosphate synthase (Tps1) converts UDP-glucose and glucose-6-phosphate to trehalose-6-phosphate. Here, we report the structures of full-length Cryptococcus neoformans Tps1 (CnTps1) in unliganded form and in complex with uridine diphosphate and glucose-6-phosphate. Comparison of these two structures reveals significant movement toward the catalytic pocket by the N terminus upon ligand binding and identifies residues required for substrate binding, as well as residues that stabilize the tetramer. Intriguingly, an intrinsically disordered domain (IDD), which is conserved among Cryptococcal species and closely related basidiomycetes, extends from each subunit of the tetramer into the "solvent" but is not visible in density maps. We determined that the IDD is not required for C. neoformans Tps1-dependent thermotolerance and osmotic stress survival. Studies with UDP-galactose highlight the exquisite substrate specificity of CnTps1. In toto, these studies expand our knowledge of trehalose biosynthesis in Cryptococcus and highlight the potential of developing antifungal therapeutics that disrupt the synthesis of this disaccharide or the formation of a functional tetramer and the use of cryo-EM in the structural characterization of CnTps1-ligand/drug complexes.

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Published In

Proc Natl Acad Sci U S A

DOI

EISSN

1091-6490

Publication Date

August 6, 2024

Volume

121

Issue

32

Start / End Page

e2314087121

Location

United States

Related Subject Headings

  • Trehalose
  • Models, Molecular
  • Humans
  • Glucosyltransferases
  • Fungal Proteins
  • Crystallography, X-Ray
  • Cryptococcus neoformans
  • Catalytic Domain
  • Antifungal Agents
 

Citation

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ICMJE
MLA
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Washington, E. J., Zhou, Y., Hsu, A. L., Petrovich, M., Tenor, J. L., Toffaletti, D. L., … Brennan, R. G. (2024). Structures of trehalose-6-phosphate synthase, Tps1, from the fungal pathogen Cryptococcus neoformans: A target for antifungals. Proc Natl Acad Sci U S A, 121(32), e2314087121. https://doi.org/10.1073/pnas.2314087121
Washington, Erica J., Ye Zhou, Allen L. Hsu, Matthew Petrovich, Jennifer L. Tenor, Dena L. Toffaletti, Ziqiang Guan, et al. “Structures of trehalose-6-phosphate synthase, Tps1, from the fungal pathogen Cryptococcus neoformans: A target for antifungals.Proc Natl Acad Sci U S A 121, no. 32 (August 6, 2024): e2314087121. https://doi.org/10.1073/pnas.2314087121.
Washington EJ, Zhou Y, Hsu AL, Petrovich M, Tenor JL, Toffaletti DL, et al. Structures of trehalose-6-phosphate synthase, Tps1, from the fungal pathogen Cryptococcus neoformans: A target for antifungals. Proc Natl Acad Sci U S A. 2024 Aug 6;121(32):e2314087121.
Washington, Erica J., et al. “Structures of trehalose-6-phosphate synthase, Tps1, from the fungal pathogen Cryptococcus neoformans: A target for antifungals.Proc Natl Acad Sci U S A, vol. 121, no. 32, Aug. 2024, p. e2314087121. Pubmed, doi:10.1073/pnas.2314087121.
Washington EJ, Zhou Y, Hsu AL, Petrovich M, Tenor JL, Toffaletti DL, Guan Z, Perfect JR, Borgnia MJ, Bartesaghi A, Brennan RG. Structures of trehalose-6-phosphate synthase, Tps1, from the fungal pathogen Cryptococcus neoformans: A target for antifungals. Proc Natl Acad Sci U S A. 2024 Aug 6;121(32):e2314087121.
Journal cover image

Published In

Proc Natl Acad Sci U S A

DOI

EISSN

1091-6490

Publication Date

August 6, 2024

Volume

121

Issue

32

Start / End Page

e2314087121

Location

United States

Related Subject Headings

  • Trehalose
  • Models, Molecular
  • Humans
  • Glucosyltransferases
  • Fungal Proteins
  • Crystallography, X-Ray
  • Cryptococcus neoformans
  • Catalytic Domain
  • Antifungal Agents