New ShK-like peptide from the jellyfish Nemopilema nomurai has human potassium voltage-gated channel-blocking activity

DC Field Value Language
dc.contributor.author Ye-Ji Kim -
dc.contributor.author Jo, Ye Jin -
dc.contributor.author Seung Eun Lee -
dc.contributor.author Jungeun Kim -
dc.contributor.author Jae-Pil Choi -
dc.contributor.author Nayoung Lee -
dc.contributor.author Won, Hyokyoung -
dc.contributor.author Dong Ho Woo -
dc.contributor.author Yum, Seung Shic -
dc.date.accessioned 2023-11-17T06:30:21Z -
dc.date.available 2023-11-17T06:30:21Z -
dc.date.created 2023-11-09 -
dc.date.issued 2023-11-08 -
dc.identifier.uri https://sciwatch.kiost.ac.kr/handle/2020.kiost/44831 -
dc.description.abstract We have identified a new human voltage-gated potassium channel (hKv1.3) blocker, NnK-1 (CKDHHTYGVY10CKDWKSSGEC20KKNPKGMRHF30CRKTCGFC38), in the jellyfish Nemopilema nomurai, based on its genomic information. The gene sequence encoding NnK-1 contains 5,408 base pairs, with five introns and six exons. The coding sequence of the NnK-1 precursor is 894 nucleotides long and encodes 297 amino acids, containing five presumptive ShK-like peptides. An electrophysiological assay demonstrated that the chemically synthesized fifth peptide, NnK-1, is an effective hKv1.3 blocker. A multiple sequence alignment with cnidarian Shk-like peptides, which have Kv1.3-blocking activity, revealed that four residues (3Asp, 25Lys, 33Lys, and 34Thr) of NnK-1, together with six cysteine residues, are conserved. Therefore, we hypothesize that these four residues are crucial for the binding of the toxins to voltage-gated potassium channels. -
dc.description.uri 2 -
dc.language Korean -
dc.publisher 대한 독성 유전·단백체학회 -
dc.relation.isPartOf 2023 The 19th International Conference on Toxicogenomics Abstrack Book -
dc.title New ShK-like peptide from the jellyfish Nemopilema nomurai has human potassium voltage-gated channel-blocking activity -
dc.type Conference -
dc.citation.conferenceDate 2023-11-07 -
dc.citation.conferencePlace KO -
dc.citation.conferencePlace ICC호텔, 대전 -
dc.citation.endPage 148 -
dc.citation.startPage 148 -
dc.citation.title 2023 The 19th International Conference on Toxicogenomics(ICT-2023) -
dc.contributor.alternativeName 조예진 -
dc.contributor.alternativeName 이나영 -
dc.contributor.alternativeName 원효경 -
dc.contributor.alternativeName 염승식 -
dc.identifier.bibliographicCitation 2023 The 19th International Conference on Toxicogenomics(ICT-2023), pp.148 -
dc.description.journalClass 2 -
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South Sea Research Institute > Risk Assessment Research Center > 2. Conference Papers
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