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Details

Autor(en) / Beteiligte
Titel
Scorpion Potassium Channel-blocking Defensin Highlights a Functional Link with Neurotoxin
Ist Teil von
  • The Journal of biological chemistry, 2016-03, Vol.291 (13), p.7097-7106
Ort / Verlag
United States: Elsevier Inc
Erscheinungsjahr
2016
Quelle
MEDLINE
Beschreibungen/Notizen
  • The structural similarity between defensins and scorpion neurotoxins suggests that they might have evolved from a common ancestor. However, there is no direct experimental evidence demonstrating a functional link between scorpion neurotoxins and defensins. The scorpion defensin BmKDfsin4 from Mesobuthus martensii Karsch contains 37 amino acid residues and a conserved cystine-stabilized α/β structural fold. The recombinant BmKDfsin4, a classical defensin, has been found to have inhibitory activity against Gram-positive bacteria such as Staphylococcus aureus, Bacillus subtilis, and Micrococcus luteus as well as methicillin-resistant Staphylococcus aureus. Interestingly, electrophysiological experiments showed that BmKDfsin4,like scorpion potassium channel neurotoxins, could effectively inhibit Kv1.1, Kv1.2, and Kv1.3 channel currents, and its IC50 value for the Kv1.3 channel was 510.2 nm. Similar to the structure-function relationships of classical scorpion potassium channel-blocking toxins, basic residues (Lys-13 and Arg-19) of BmKDfsin4 play critical roles in peptide-Kv1.3 channel interactions. Furthermore, mutagenesis and electrophysiological experiments demonstrated that the channel extracellular pore region is the binding site of BmKDfsin4, indicating that BmKDfsin4adopts the same mechanism for blocking potassium channel currents as classical scorpion toxins. Taken together, our work identifies scorpion BmKDfsin4 as the first invertebrate defensin to block potassium channels. These findings not only demonstrate that defensins from invertebrate animals are a novel type of potassium channel blockers but also provide evidence of a functional link between defensins and neurotoxins.
Sprache
Englisch
Identifikatoren
ISSN: 0021-9258
eISSN: 1083-351X
DOI: 10.1074/jbc.M115.680611
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4807291
Format
Schlagworte
Amino Acid Sequence, Animals, Anti-Bacterial Agents - chemistry, Anti-Bacterial Agents - metabolism, Anti-Bacterial Agents - pharmacology, Bacillus subtilis - drug effects, Bacillus subtilis - growth & development, bacteria, Cell Biology, defensin, Defensins - chemistry, Defensins - genetics, Defensins - metabolism, Defensins - pharmacology, Gene Expression, Humans, Kv1.1 Potassium Channel - antagonists & inhibitors, Kv1.1 Potassium Channel - genetics, Kv1.1 Potassium Channel - metabolism, Kv1.2 Potassium Channel - antagonists & inhibitors, Kv1.2 Potassium Channel - genetics, Kv1.2 Potassium Channel - metabolism, Kv1.3 Potassium Channel - antagonists & inhibitors, Kv1.3 Potassium Channel - genetics, Kv1.3 Potassium Channel - metabolism, Methicillin-Resistant Staphylococcus aureus - drug effects, Methicillin-Resistant Staphylococcus aureus - growth & development, Mice, Micrococcus luteus - drug effects, Micrococcus luteus - growth & development, Models, Molecular, Molecular Sequence Data, neurotoxin, Neurotoxins - chemistry, Neurotoxins - genetics, Neurotoxins - metabolism, Neurotoxins - pharmacology, potassium channel, Potassium Channel Blockers - chemistry, Potassium Channel Blockers - metabolism, Potassium Channel Blockers - pharmacology, Protein Interaction Domains and Motifs, Protein Structure, Secondary, Recombinant Proteins - chemistry, Recombinant Proteins - genetics, Recombinant Proteins - metabolism, Recombinant Proteins - pharmacology, Scorpion Venoms - biosynthesis, Scorpion Venoms - chemistry, Scorpions - chemistry, Scorpions - physiology, Sequence Alignment, Staphylococcus aureus - drug effects, Staphylococcus aureus - growth & development, Structural Homology, Protein, Structure-Activity Relationship, structure-function

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