| Literature DB >> 27738055 |
Alejandro Castellanos-Gonzalez1, Hayley Sparks1, Samantha Nava1, Wenlin Huang2, Zhongsheng Zhang2, Kasey Rivas2, Matthew A Hulverson2, Lynn K Barrett2, Kayode K Ojo2, Erkang Fan2, Wesley C Van Voorhis2, Arthur Clinton White1.
Abstract
Cryptosporidium is recognized as one of the main causes of childhood diarrhea worldwide. However, the current treatment for cryptosporidiosis is suboptimal. Calcium flux is essential for entry in apicomplexan parasites. Calcium-dependent protein kinases (CDPKs) are distinct from protein kinases of mammals, and the CDPK1 of the apicomplexan Cryptosporidium lack side chains that typically block a hydrophobic pocket in protein kinases. We exploited this to develop bumped kinase inhibitors (BKIs) that selectively target CDPK1. We have shown that several BKIs of Cryptosporidium CDPK1 potently reduce enzymatic activity and decrease parasite numbers when tested in vitro. In the present work, we studied the anticryptosporidial activity of BKI-1517, a novel BKI. The half maximal effective concentration for Cryptosporidium parvum in HCT-8 cells was determined to be approximately 50 nM. Silencing experiments of CDPK1 suggest that BKI-1517 acts on CDPK1 as its primary target. In a mouse model of chronic infection, 5 of 6 SCID/beige mice (83.3%) were cured after treatment with a single daily dose of 120 mg/kg BKI-1517. No side effects were observed. These data support advancing BKI-1517 as a lead compound for drug development for cryptosporidiosis.Entities:
Keywords: BKI; CDPK; CDPK1; cryptosporidiosis; cryptosporidium; kinase inhibitors; siRNA
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Year: 2016 PMID: 27738055 PMCID: PMC5142094 DOI: 10.1093/infdis/jiw481
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226