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Identification of an HV 1 voltage-gated proton channel in insects.
Chaves, Gustavo; Derst, Christian; Franzen, Arne; Mashimo, Yuta; Machida, Ryuichiro; Musset, Boris.
Afiliação
  • Chaves G; Institute of Complex Systems, Zelluläre Biophysik (ICS-4) Forschungszentrum Jülich, Germany.
  • Derst C; Zoologisches Institut, Biozentrum Universität zu Köln, Germany.
  • Franzen A; Institute of Complex Systems, Zelluläre Biophysik (ICS-4) Forschungszentrum Jülich, Germany.
  • Mashimo Y; Sugadaira Montane Research Center, University of Tsukuba, Ueda, Japan.
  • Machida R; Sugadaira Montane Research Center, University of Tsukuba, Ueda, Japan.
  • Musset B; Institute of Complex Systems, Zelluläre Biophysik (ICS-4) Forschungszentrum Jülich, Germany.
FEBS J ; 283(8): 1453-64, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26866814
ABSTRACT
UNLABELLED The voltage-gated proton channel 1 (HV 1) is an important component of the cellular proton extrusion machinery and is essential for charge compensation during the respiratory burst of phagocytes. HV 1 has been identified in a wide range of eukaryotes throughout the animal kingdom, with the exception of insects. Therefore, it has been proposed that insects do not possess an HV 1 channel. In the present study, we report the existence of an HV 1-type proton channel in insects. We searched insect transcriptome shotgun assembly (TSA) sequence databases and found putative HV 1 orthologues in various polyneopteran insects. To confirm that these putative HV 1 orthologues were functional channels, we studied the HV 1 channel of Nicoletia phytophila (NpHV 1), an insect of the Zygentoma order, in more detail. NpHV 1 comprises 239 amino acids and is 33% identical to the human voltage-gated proton channel 1. Patch clamp measurements in a heterologous expression system showed proton selectivity, as well as pH- and voltage-dependent gating. Interestingly, NpHV 1 shows slightly enhanced pH-dependent gating compared to the human channel. Mutations in the first transmembrane segment at position 66 (Asp66), the presumed selectivity filter, lead to a loss of proton-selective conduction, confirming the importance of this aspartate residue in voltage-gated proton channels. DATABASE Nucleotide sequence data have been deposited in the GenBank database under accession number KT780722.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Prótons / Ativação do Canal Iônico / Membrana Celular / Insetos / Canais Iônicos / Potenciais da Membrana Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Prótons / Ativação do Canal Iônico / Membrana Celular / Insetos / Canais Iônicos / Potenciais da Membrana Idioma: En Ano de publicação: 2016 Tipo de documento: Article