In this study, we evaluated the impact of incorporating diblock and triblock amphiphilic copolymers, as well as cholesterol into DPPC liposomes on the release of a model molecule, calcein, mediated by exogenous phospholipase A2 activity. Our findings show that calcein release slows down in the presence of copolymers at low concentration, while at high concentration, the calcein release profile resembles that of the DPPC control. Additionally, calcein release mediated by exogenous PLA2 decreases as the amount of solubilized cholesterol increases, with a maximum between 18 mol% and 20 mol%.
View Article and Find Full Text PDFSequences derived from parvoviruses (family ) are relatively common in animal genomes, but the functional significance of these endogenous parvoviral element (EPV) sequences remains unclear. In this study, we used a combination of and molecular biological approaches to investigate a fusion gene carried by guinea pigs (genus ) that is partially derived from an EPV. This gene, named , encodes a predicted polypeptide gene product comprising a partial 9-like () gene fused to a 3' truncated, EPV-encoded replicase.
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