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1 bsorbance properties compared with authentic indolicidin.
2 rinated analogs of the antibacterial peptide indolicidin.
3 al partitioning free energies of variants of indolicidin, a cationic proline-rich antimicrobial pepti
5 ations are the principal structural motif of indolicidin and that these turns greatly enhance membran
6 ture of the cross-linked byproduct, termed X-indolicidin, by absorbance and fluorescence spectroscopy
10 tryptophan, we synthesized indolicidin-L and indolicidin-F in which all five tryptophans were replace
13 teps and was shown be identical to authentic indolicidin in its microbicidal activity against Staphyl
15 helix formation in the CD spectra of native indolicidin in various solvents or when bound to micelle
16 Consistent with experimental observations, indolicidin induces membrane thinning, although the simu
17 etric footprinting approaches, we found that indolicidin interferes with formation of the catalytic i
21 s associated with tryptophan, we synthesized indolicidin-L and indolicidin-F in which all five trypto
24 cluding melittin, fowlicidin-1, tritrpticin, indolicidin, puroindoline A peptide, magainin II F5W, la
25 tructured cationic peptides, because five of indolicidin's 13 residues are tryptophans: H-Ile-Leu-Pro
26 a 2-atomic mass unit reduction compared with indolicidin, suggesting the deprotonation of two indole
28 dependent of the PWWP motif but involves the indolicidin unique lysine residue and the N- and C- term
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