A Glycosylated, Labionin-Containing Lanthipeptide with Marked Antinociceptive Activity

Marianna Iorio, Oscar Sasso, Sonia I. Maffioli, Rosalia Bertorelli, Paolo Monciardini, Margherita Sosio, Fabiola Bonezzi, Maria Summa, Cristina Brunati, Roberta Bordoni,

ACS Chemical Biology · 2013 · 99 citations · 21 references

Concepts

Abstract

Among the growing family of ribosomally synthesized, post-translationally modified peptides, particularly intriguing are class III lanthipeptides containing the triamino acid labionin. In the course of a screening program aimed at finding bacterial cell wall inhibitors, we discovered a new lanthipeptide produced by an Actinoplanes sp. The molecule, designated NAI-112, consists of 22 amino acids and contains an N-terminal labionin and a C-terminal methyl-labionin. Unique among lanthipeptides, it carries a 6-deoxyhexose moiety N-linked to a tryptophan residue. Consistently, the corresponding gene cluster encodes, in addition to the LanKC enzyme characteristic of this lanthipeptide class, a glycosyl transferase. Despite possessing weak antibacterial activity, NAI-112 is effective in experimental models of nociceptive pain, reducing pain symptoms in mice in both the formalin and the chronic constriction injury tests. Thus, NAI-112 represents, after the labyrinthopeptins, the second example of a lanthipeptide effective against nociceptive pain.

References

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