| Literature DB >> 27424215 |
Ji-Hyun Yeom1, Boeun Lee1, Daeyoung Kim1, Jong-Kook Lee2, Suk Kim3, Jeehyeon Bae4, Yoonkyung Park5, Kangseok Lee6.
Abstract
Antimicrobial peptides (AMPs) are a promising new class of antibacterial compounds. However, their applications in the treatment of intracellular pathogenic bacteria have been limited by their in vivo instability and low penetrating ability into mammalian cells. Here, we report that gold nanoparticles conjugated with DNA aptamer (AuNP-Apt) efficiently delivered AMPs into mammalian living systems with enhanced stability of the AMPs. C-terminally hexahistidine-tagged A3-APO (A3-APO(His)) AMPs were loaded onto AuNPs conjugated with His-tag DNA aptamer (AuNP-Apt(His)) by simple mixing and were delivered into Salmonella enterica serovar Typhimurium (S. Typhimurium)-infected HeLa cells, resulting in the increased viability of host cells due to the elimination of intracellular S. Typhimurium cells. Furthermore, the intravenous injection of AuNP-Apt(His) loaded with A3-APO(His) into S. Typhimurium-infected mice resulted in a complete inhibition of S. Typhimurium colonization in the mice organs, leading to 100% survival of the mice. Therefore, AuNP-Apt(His) can serve as an innovative platform for AMP therapeutics to treat intracellular bacterial infections in mammals.Entities:
Keywords: A3-APO; Antimicrobial peptides; Gold-nanoparticle; S.Typhimurium
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Year: 2016 PMID: 27424215 DOI: 10.1016/j.biomaterials.2016.07.009
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479