Fluorescent Ligands of Kv1 Channels on the Basis of Hongotoxin: Atto488-Hongotoxin
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[1] Yuliya V. Korolkova,et al. Complexes of Peptide Blockers with Kv1.6 Pore Domain: Molecular Modeling and Studies with KcsA-Kv1.6 Channel , 2017, Journal of Neuroimmune Pharmacology.
[2] E. Grishin,et al. Variability of Potassium Channel Blockers in Mesobuthus eupeus Scorpion Venom with Focus on Kv1.1 , 2015, The Journal of Biological Chemistry.
[3] E. Grishin,et al. Fluorescent system based on bacterial expression of hybrid KcsA channels designed for Kv1.3 ligand screening and study , 2013, Analytical and Bioanalytical Chemistry.
[4] E. Grishin,et al. Recombinant Kv Channels at the Membrane of Escherichia coli Bind Specifically Agitoxin2 , 2009, Journal of Neuroimmune Pharmacology.
[5] Olaf Pongs,et al. Engineering-specific pharmacological binding sites for peptidyl inhibitors of potassium channels into KcsA. , 2002, Biochemistry.
[6] G. Schütz,et al. Synthesis, characterization, and application of cy-dye- and alexa-dye-labeled hongotoxin(1) analogues. The first high affinity fluorescence probes for voltage-gated K+ channels. , 2002, Bioconjugate chemistry.
[7] G. Schütz,et al. Ultrasensitive pharmacological characterisation of the voltage-gated potassium channel KV1.3 studied by single-molecule fluorescence microscopy , 2002, Histochemistry and Cell Biology.
[8] A. Koschak,et al. Subunit Composition of Brain Voltage-gated Potassium Channels Determined by Hongotoxin-1, a Novel Peptide Derived fromCentruroides limbatus Venom* , 1998, The Journal of Biological Chemistry.