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A study of effects of peptide fragments of bovine and human lactoferrins on activities of three key HIV-1 enzymes.
- Source :
-
Peptides [Peptides] 2014 Dec; Vol. 62, pp. 183-8. - Publication Year :
- 2014
-
Abstract
- The intent of this study was to examine human and bovine lactoferrin fragments including lactoferrin (1-11), lactoferricin and lactoferrampin, all of which did not demonstrate hemolytic activity toward rabbit erythrocytes at 1 mM concentration, for possible inhibitory effects on the activities of HIV-1 reverse transcriptase, protease and integrase. The data showed that human lactoferricin was the most potent in inhibiting HIV-1 reverse transcriptase (IC50 =2 μM). Bovine lactoferricin (IC50 = 10 μM) and bovine lactoferrampin (IC50 = 150 μM) were less potent. Human lactoferrampin and human and bovine lactoferrin (1-11) at 1 mM concentration did not exhibit any inhibitory effect on HIV-1 reverse transcriptase. All peptides showed only a slight inhibitory effect (from slightly below 2% to 6% inhibition) on HIV-1 protease. Human lactoferrampin and bovine lactoferrampin showed obvious inhibitory effect on HIV-1 integrase at 37 μM and 18.5 μM, respectively. The HIV-1 integrase inhibitory activity of human lactoferrampin and bovine lactoferrampin was dose-dependent. The other peptides were devoid of HIV-1 integrase inhibitory activity. Thus, it is concluded that some lactoferrin fragments exert an inhibitory action on HIV-1 reverse transcriptase and HIV-1 integrase.
- Subjects :
- Amino Acid Sequence
Animals
Cattle
Erythrocytes drug effects
HIV Integrase drug effects
HIV Protease drug effects
HIV Reverse Transcriptase antagonists & inhibitors
Humans
Lactoferrin genetics
Peptide Fragments genetics
Rabbits
HIV-1 drug effects
HIV-1 enzymology
Lactoferrin administration & dosage
Peptide Fragments administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 1873-5169
- Volume :
- 62
- Database :
- MEDLINE
- Journal :
- Peptides
- Publication Type :
- Academic Journal
- Accession number :
- 25445609
- Full Text :
- https://doi.org/10.1016/j.peptides.2014.07.006