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Investigating the nucleic acid interactions of histone-derived antimicrobial peptides.

ABSTRACT: While many antimicrobial peptides (AMPs) disrupt bacterial membranes, some translocate into bacteria and interfere with intracellular processes. Buforin II and DesHDAP1 are thought to kill bacteria by interacting with nucleic acids. Here, molecular modeling and experimental measurements are used to show that neither nucleic acid binding peptide selectively binds DNA sequences. Simulations and experiments also show that changing lysines to arginines enhances DNA binding, suggesting that including additional guanidinium groups is a potential strategy to engineer more potent AMPs. Moreover, the lack of binding specificity may make it more difficult for bacteria to evolve resistance to these and other similar AMPs.

SUBMITTER: Sim S

PROVIDER: S-EPMC5371511 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature

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Investigating the nucleic acid interactions of histone-derived antimicrobial peptides.

Sim Sukin S Wang Penny P Beyer Brittany N BN Cutrona Kara J KJ Radhakrishnan Mala L ML Elmore Donald E DE

FEBS letters 20170301 5

While many antimicrobial peptides (AMPs) disrupt bacterial membranes, some translocate into bacteria and interfere with intracellular processes. Buforin II and DesHDAP1 are thought to kill bacteria by interacting with nucleic acids. Here, molecular modeling and experimental measurements are used to show that neither nucleic acid binding peptide selectively binds DNA sequences. Simulations and experiments also show that changing lysines to arginines enhances DNA binding, suggesting that including ...[more]

PMID: 28130840

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