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Surface expression and subunit specific control of steady protein levels by the Kv7.2 helix A-B linker.
Aivar, Paloma; Fernández-Orth, Juncal; Gomis-Perez, Carolina; Alberdi, Araitz; Alaimo, Alessandro; Rodríguez, Manuel S; Giraldez, Teresa; Miranda, Pablo; Areso, Pilar; Villarroel, Alvaro.
Afiliação
  • Aivar P; Unidad de Biofísica, CSIC, UPV/EHU, Universidad del País Vasco, Barrio Sarriena s/n, Leioa, Spain.
PLoS One ; 7(10): e47263, 2012.
Article em En | MEDLINE | ID: mdl-23115641
Kv7.2 and Kv7.3 are the main components of the neuronal voltage-dependent M-current, which is a subthreshold potassium conductance that exerts an important control on neuronal excitability. Despite their predominantly intracellular distribution, these channels must reach the plasma membrane in order to control neuronal activity. Thus, we analyzed the amino acid sequence of Kv7.2 to identify intrinsic signals that may control its surface expression. Removal of the interlinker connecting helix A and helix B of the intracellular C-terminus produces a large increase in the number of functional channels at the plasma membrane. Moreover, elimination of this linker increased the steady-state amount of protein, which was not associated with a decrease of protein degradation. The magnitude of this increase was inversely correlated with the number of helix A - helix B linkers present in the tetrameric channel assemblies. In contrast to the remarkable effect on the amount of Kv7.2 protein, removal of the Kv7.2 linker had no detectable impact on the steady-state levels of Kv7.3 protein.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canal de Potássio KCNQ2 Limite: Animals / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Espanha País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canal de Potássio KCNQ2 Limite: Animals / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Espanha País de publicação: Estados Unidos