Teixobactin is a head to side chain cyclodepsipeptide that contains two positive charges. One is found in the cycle, as a result of the presence of the guanidino-unusual amino acid L-allo-End, while the other is at the N-terminal. Here we introduce 26 new Teixobactin analogues with an increasing number of positive charges. In an attempt to fine-tune the biological activity of Teixobactin, we examined the effect of cationicity on the SAR of these analogues. The maximum number of positive charges to maintain the activity are three to four. Analogues with five positive charges show the lowest activity.
Teixobactin
is a recently discovered antimicrobial cyclodepsipeptide
with good activity against Gram positive bacteria. Taking Arg10–teixobactin as
a reference, where the nonproteinogenic residue l-allo-enduracididine
was substituted by arginine, a lysine scan was performed to identify
the importance of keeping the balance between hydrophilic and hydrophobic
amino acids for the antimicrobial activities of this peptide family.
Thus, the substitution of four isoleucine residues present in the
natural sequence by lysine led to a total loss of activity. On the
other hand, the substitution of the polar noncharged residues and
alanine by lysine allowed us to keep and in some cases to improve
the antimicrobial activity.
Teixobactin is a head to side-chain cyclic depsipeptide with a guanidino based residue within the cycle, three d-amino acids in the tail, and a N-methylated terminal residue.
Teixobactin is a recently described antimicrobial peptide that shows high activity against gram-positive bacteria as well as mycobacterium tuberculosis. Due to both its structure as a head-to-side chain cyclodepsipeptide and its activity, it has attracted the attention of several research groups. In this regard, a large number of analogs with substitutions in both the cycle and the tail has been described. Here, we report the contribution of the N-terminus residue, N-Me-d-Phe, to the activity of Arg10-teixobactin. On the basis of our findings, we conclude that the N-terminus accepts minimum changes but not the presence of long alkyl chains. The presence of a positive charge is a requirement for the activity of the peptide. Furthermore, acylation of the N-terminus leads to total loss of activity.
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