کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2006369 1066336 2010 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Interaction of cationic antimicrobial peptides with phospholipid vesicles and their antibacterial activity
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Interaction of cationic antimicrobial peptides with phospholipid vesicles and their antibacterial activity
چکیده انگلیسی

We have designed and synthesized a series of cationic α-helical AMPs with improved antibacterial activity and selectivity against a broad spectrum of G(+) and G(−) bacteria. In the current study, we intended to gain further insight into the mechanisms of action between AMPs and cellular membranes using model liposomes of various phospholipid compositions. Circular dichroism measurements showed that AMPs adopted amphipathic α-helical conformation in the presence of negatively charged vesicles (DOPC/DOPG = 1:3), while they were largely unstructured when incubated with neutral vesicles (DOPC). The interaction of AMPs with phospholipid vesicles were further analyzed by calcein leakage experiments. AMPs exhibited weak dye-leakage activity for DOPC (neutral) vesicles, while they effectively induced calcein leakage when interacted with DOPC/DOPG-entrapped vesicles. These results indicated that our newly designed cationic AMPs did show preferences for bacteria-mimicking anionic membranes. All of them exert their cytolytic activity by folding into an amphipathic helix upon selectively binding and insertion into the target membrane, leading to breakdown of the membrane structure, thus causing leakage of cell contents, resulting finally in cell death. Elucidating the mechanism of the membranolytic activity of AMPs may facilitate the development of more effective antimicrobial agents.

Research highlights▶ Cationic AMPs adopt amphipathic α-helical conformation in the presence of negatively charged vesicles (DOPC/DOPG = 1:3). ▶ Cationic AMPs effectively induce calcein-leakage when interacted with DOPC/DOPG-entrapped vesicles. ▶ Cationic AMPs show preferences for bacteria-mimicking anionic membranes. ▶ Cationic AMPs exert their cytolytic activity by folding into an amphipathic helix upon selectively binding and insertion into the target membrane, leading to breakdown of the membrane structure, thus causing leakage of cell contents, resulting finally in cell death. ▶ Elucidating the mechanism of the membranolytic activity of cationic AMPs may facilitate the development of more effective antimicrobial agents.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Peptides - Volume 31, Issue 10, October 2010, Pages 1811–1820
نویسندگان
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