Excretion/secretion products from Schistosoma mansoni adults, eggs and schistosomula have unique peptidase specificity profiles
Jazyk angličtina Země Francie Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
P41 GM103481
NIGMS NIH HHS - United States
8P41GM103481
NIGMS NIH HHS - United States
R21 AI107390
NIAID NIH HHS - United States
R01AI089896
NIAID NIH HHS - United States
R21AI107390
NIAID NIH HHS - United States
R01 AI089896
NIAID NIH HHS - United States
PubMed
26409899
PubMed Central
PMC4747843
DOI
10.1016/j.biochi.2015.09.025
PII: S0300-9084(15)00300-4
Knihovny.cz E-zdroje
- Klíčová slova
- Excretion, Fluke, Inhibitor, Parasite, Protease, Secretion,
- MeSH
- interakce hostitele a patogenu MeSH
- lidé MeSH
- molekulární sekvence - údaje MeSH
- ovum metabolismus MeSH
- proteasy metabolismus MeSH
- proteiny červů metabolismus MeSH
- proteolýza MeSH
- Schistosoma mansoni růst a vývoj metabolismus fyziologie MeSH
- schistosomiasis mansoni parazitologie MeSH
- sekvence aminokyselin MeSH
- stadia vývoje MeSH
- substrátová specifita MeSH
- vazebná místa MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- proteasy MeSH
- proteiny červů MeSH
Schistosomiasis is one of a number of chronic helminth diseases of poverty that severely impact personal and societal well-being and productivity. Peptidases (proteases) are vital to successful parasitism, and can modulate host physiology and immunology. Interference of peptidase action by specific drugs or vaccines can be therapeutically beneficial. To date, research on peptidases in the schistosome parasite has focused on either the functional characterization of individual peptidases or their annotation as part of global genome or transcriptome studies. We were interested in functionally characterizing the complexity of peptidase activity operating at the host-parasite interface, therefore the excretory-secretory products of key developmental stages of Schistosoma mansoni that parasitize the human were examined. Using class specific peptidase inhibitors in combination with a multiplex substrate profiling assay, a number of unique activities derived from endo- and exo-peptidases were revealed in the excretory-secretory products of schistosomula (larval migratory worms), adults and eggs. The data highlight the complexity of the functional degradome for each developmental stage of this parasite and facilitate further enquiry to establish peptidase identity, physiological and immunological function, and utility as drug or vaccine candidates.
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