Unknown

Dataset Information

0

Structure and function of papiliocin with antimicrobial and anti-inflammatory activities isolated from the swallowtail butterfly, Papilio xuthus.


ABSTRACT: Papiliocin is a novel 37-residue cecropin-like peptide isolated recently from the swallowtail butterfly, Papilio xuthus. With the aim of identifying a potent antimicrobial peptide, we tested papiliocin in a variety of biological and biophysical assays, demonstrating that the peptide possesses very low cytotoxicity against mammalian cells and high bacterial cell selectivity, particularly against Gram-negative bacteria as well as high anti-inflammatory activity. Using LPS-stimulated macrophage RAW264.7 cells, we found that papiliocin exerted its anti-inflammatory activities by inhibiting nitric oxide (NO) production and secretion of tumor necrosis factor (TNF)-? and macrophage inflammatory protein (MIP)-2, producing effects comparable with those of the antimicrobial peptide LL-37. We also showed that the innate defense response mechanisms engaged by papiliocin involve Toll-like receptor pathways that culminate in the nuclear translocation of NF-?B. Fluorescent dye leakage experiments showed that papiliocin targets the bacterial cell membrane. To understand structure-activity relationships, we determined the three-dimensional structure of papiliocin in 300 mm dodecylphosphocholine micelles by NMR spectroscopy, showing that papiliocin has an ?-helical structure from Lys(3) to Lys(21) and from Ala(25) to Val(36), linked by a hinge region. Interactions between the papiliocin and LPS studied using tryptophan blue-shift data, and saturation transfer difference-NMR experiments revealed that Trp(2) and Phe(5) at the N-terminal helix play an important role in attracting papiliocin to the cell membrane of Gram-negative bacteria. In conclusion, we have demonstrated that papiliocin is a potent peptide antibiotic with both anti-inflammatory and antibacterial activities, and we have laid the groundwork for future studies of its mechanism of action.

SUBMITTER: Kim JK 

PROVIDER: S-EPMC3308842 | biostudies-literature | 2011 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Structure and function of papiliocin with antimicrobial and anti-inflammatory activities isolated from the swallowtail butterfly, Papilio xuthus.

Kim Jin-Kyoung JK   Lee Eunjung E   Shin Soyoung S   Jeong Ki-Woong KW   Lee Jee-Young JY   Bae Su-Young SY   Kim Soo-Hyun SH   Lee Juneyoung J   Kim Seong Ryul SR   Lee Dong Gun DG   Hwang Jae-Sam JS   Kim Yangmee Y  

The Journal of biological chemistry 20110929 48


Papiliocin is a novel 37-residue cecropin-like peptide isolated recently from the swallowtail butterfly, Papilio xuthus. With the aim of identifying a potent antimicrobial peptide, we tested papiliocin in a variety of biological and biophysical assays, demonstrating that the peptide possesses very low cytotoxicity against mammalian cells and high bacterial cell selectivity, particularly against Gram-negative bacteria as well as high anti-inflammatory activity. Using LPS-stimulated macrophage RAW  ...[more]

Similar Datasets

2012-05-12 | GSE37920 | GEO
2012-05-11 | E-GEOD-37920 | biostudies-arrayexpress
| S-EPMC7891156 | biostudies-literature
| S-EPMC3386895 | biostudies-literature
| S-EPMC4650181 | biostudies-literature
| S-EPMC7697948 | biostudies-literature
| S-EPMC3402530 | biostudies-literature
| S-EPMC10411748 | biostudies-literature
2015-08-28 | GSE65280 | GEO
| S-EPMC8046538 | biostudies-literature