Evidence map›Paper›PMID 27977806›Full record

ArticlePLoS pathogens2016

Integrated Activity and Genetic Profiling of Secreted Peptidases in Cryptococcus neoformans Reveals an Aspartyl Peptidase Required for Low pH Survival and Virulence.

Starlynn C Clarke, Phillip A Dumesic, Christina M Homer, Anthony J O'Donoghue, Florencia La Greca, Lenka Pallova, Pavel Majer, Hiten D Madhani, Charles S Craik

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Insights from Mass Spectrometry-Based Proteomics onJournal of fungi (Basel, Switzerland) · 2025
    Review
  5. On-Resin Assembly of Macrocyclic Inhibitors ofJournal of medicinal chemistry · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Secretome analysis and virulence assessment inJournal of oral microbiology · 2024
    Article
  11. Article
  12. Review
  13. Secreted peptidases contribute to virulence of fish pathogenFrontiers in cellular and infection microbiology · 2023
    Article
  14. Article
  15. The human pathobiontProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Article
  17. Review
  18. Article
  19. Re-emerging Aspartic Protease Targets: ExaminingJournal of medicinal chemistry · 2021
    Article
  20. Aspartic peptidase ofJournal of enzyme inhibition and medicinal chemistry · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Starlynn C ClarkeDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California, United States of America.
Phillip A DumesicDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, California, United States of America.
Christina M HomerDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, California, United States of America.
Anthony J O'DonoghueDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California, United States of America.
Florencia La GrecaDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California, United States of America.
Lenka PallovaInstitute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Pavel MajerInstitute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Hiten D MadhaniDepartment of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, California, United States of America.
Charles S CraikDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California, United States of America.
University of California, San Francisco · USCzech Academy of Sciences, Institute of Organic Chemistry and Biochemistry · CZ

Funding

X-ray Screening and Rapid Structure DeterminationP50GM082250 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KROGAN, NEVAN J · 2007 to 2018
$48.8M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007618 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANDERSON, MARK S · 1985 to 2020
$29.6M
Regulation of Virulence of Cryptococcus neoformansR01AI096869 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MADHANI, HITEN D · 2012 to 2016
$1.9M
NIAID NIH HHS R01 AI096869NIGMS NIH HHS P50 GM082250NIGMS NIH HHS T32 GM007618
6 · The paper itself

Abstract

The opportunistic fungal pathogen Cryptococcus neoformans is a major cause of mortality in immunocompromised individuals, resulting in more than 600,000 deaths per year. Many human fungal pathogens secrete peptidases that influence virulence, but in most cases the substrate specificity and regulation of these enzymes remains poorly understood. The paucity of such information is a roadblock to our understanding of the biological functions of peptidases and whether or not these enzymes are viable therapeutic targets. We report here an unbiased analysis of secreted peptidase activity and specificity in C. neoformans using a mass spectrometry-based substrate profiling strategy and subsequent functional investigations. Our initial studies revealed that global peptidase activity and specificity are dramatically altered by environmental conditions. To uncover the substrate preferences of individual enzymes and interrogate their biological functions, we constructed and profiled a ten-member gene deletion collection of candidate secreted peptidases. Through this deletion approach, we characterized the substrate specificity of three peptidases within the context of the C. neoformans secretome, including an enzyme known to be important for fungal entry into the brain. We selected a previously uncharacterized peptidase, which we term Major aspartyl peptidase 1 (May1), for detailed study due to its substantial contribution to extracellular proteolytic activity. Based on the preference of May1 for proteolysis between hydrophobic amino acids, we screened a focused library of aspartyl peptidase inhibitors and identified four high-affinity antagonists. Finally, we tested may1Δ strains in a mouse model of C. neoformans infection and found that strains lacking this enzyme are significantly attenuated for virulence. Our study reveals the secreted peptidase activity and specificity of an important human fungal pathogen, identifies responsible enzymes through genetic tests of their function, and demonstrates how this information can guide the development of high affinity small molecule inhibitors.

Indexed as

AnimalsAspartic Acid ProteasesCryptococcosisCryptococcus neoformansDisease Models, AnimalFungal ProteinsGene Expression ProfilingHydrogen-Ion ConcentrationImmunoblottingMass SpectrometryMicePeptide HydrolasesProteomicsReal-Time Polymerase Chain ReactionVirulenceVirulence FactorsAspartic Acid ProteasesFungal ProteinsPeptide HydrolasesVirulence Factors

Identifiers

PMID27977806
PMCPMC5158083
OpenAlexW2563625422

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.