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March 4, 2026Moscow University Biological Sciences Bulletin0 citations

N- or C-terminal Position of the Fluorescent Protein mKate2 in the mKate2-KCa3.1 Chimera Influences Membrane Expression of the Channel

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VKV. N. KorabeynikovaAFA. V. FeofanovONO. V. Nekrasova

Key Points

  • The study aims to understand how the position of mKate2 affects the membrane expression of KCa3.1 channels.
  • Constructed plasmids with KCa3.1 α-subunit fused to mKate2 at N- or C-terminus
  • Used fluorescence analysis to study membrane expression in Neuro-2a cells
  • Created fluorescent ligand ChTx-GFP from charybdotoxin and green fluorescent protein
  • mKate2 at the N-terminus inhibits KCa3.1 transport to the plasma membrane
  • mKate2 at the C-terminus allows efficient KCa3.1 accumulation and tetramer formation
  • ChTx-GFP binds to KCa3.1 at 20 nM concentration for imaging in mammalian cells

Abstract

The intermediate-conductance calcium-activated potassium channel KCa3.1 promotes calcium-dependent hyperpolarization of the cell membrane. Its malfunction has been observed in autoimmune and oncological diseases. To study this channel and its peptide blockers using fluorescence analysis, plasmids encoding the α-subunit KCa3.1 fused with the fluorescent protein mKate2 at the N- or C-terminus were constructed, and the fluorescent ligand ChTx-GFP was obtained, which is a combination of the peptide blocker charybdotoxin and the green fluorescent protein. It was found that mKate2 at the N-terminus of the α-subunit blocks the transport of the channel into the plasma membrane of Neuro-2a cells, while mKate2 at its C-terminus does not interfere with the efficient accumulation of the channel in the plasma membrane and the formation of a regular tetrameric structure capable of binding peptide blockers. The ligand ChTx-GFP binds to the KCa3.1 channel on the membrane at a concentration of 20 nM and can be used for fluorescent imaging of these channels in mammalian cells.

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Cite This Study

Korabeynikova et al. (2025) studied this question.

synapsesocial.com/papers/69a7cd1dd48f933b5eed929dhttps://doi.org/10.3103/s0096392525600978
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