Halogenation as a tool to tune antimicrobial activity of peptoids

Natalia Molchanova, Josefine Eilsø Nielsen, Kristian B. Sørensen, Bala Krishna Prabhala, Paul Robert Hansen, Reidar Lund, Annelise E. Barron*, Håvard Jenssen*

*Kontaktforfatter for dette arbejde

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Abstrakt

Antimicrobial peptides have attracted considerable interest as potential new class of antibiotics against multi-drug resistant bacteria. However, their therapeutic potential is limited, in part due to susceptibility towards enzymatic degradation and low bioavailability. Peptoids (oligomers of N-substituted glycines) demonstrate proteolytic stability and better bioavailability than corresponding peptides while in many cases retaining antibacterial activity. In this study, we synthesized a library of 36 peptoids containing fluorine, chlorine, bromine and iodine atoms, which vary by length and level of halogen substitution in position 4 of the phenyl rings. As we observed a clear correlation between halogenation of an inactive model peptoid and its increased antimicrobial activity, we designed chlorinated and brominated analogues of a known peptoid and its shorter counterpart. Short brominated analogues displayed up to 32-fold increase of the activity against S. aureus and 16- to 64-fold against E. coli and P. aeruginosa alongside reduced cytotoxicity. The biological effect of halogens seems to be linked to the relative hydrophobicity and self-assembly properties of the compounds. By small angle X-ray scattering (SAXS) we have demontrated how the self-assembled structures are dependent on the size of the halogen, degree of substitution and length of the peptoid, and correlated these features to their activity.

OriginalsprogEngelsk
Artikelnummer14805
TidsskriftScientific Reports
Vol/bind10
Udgave nummer1
Antal sider10
ISSN2045-2322
DOI
StatusUdgivet - 2020

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