Hassiki Rym, Labro Alain J, Benlasfar Zakaria, Vincke Cécile, Somia Mahmoud, El Ayeb Mohamed, Muyldermans Serge, Snyders Dirk J, Bouhaouala-Zahar Balkiss
Laboratoire des Venins et de Molécules Thérapeutiques, Institut Pasteur Tunis, University Tunis El Manar, 13 Place Pasteur, BP-74, 1002 Tunis, Tunisia.
Laboratory for Molecular Biophysics, Physiology, and Pharmacology, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.
Int J Biol Macromol. 2016 Dec;93(Pt A):167-171. doi: 10.1016/j.ijbiomac.2016.06.031. Epub 2016 Jun 16.
Voltage-gated potassium (Kv) channels form cells repolarizing power and are commonly expressed in excitable cells. In non-excitable cells, Kv channels such as Kv2.1 are involved in cell differentiation and growth. Due to the involvement of Kv2.1 in several physiological processes, these channels are promising therapeutic targets. To develop Kv2.1 specific antibody-based channel modulators, we applied a novel approach and immunized a dromedary with heterologous Ltk- cells that overexpress the mouse Kv2.1 channel instead of immunizing with channel protein fragments. The advantage of this approach is that the channel is presented in its native tetrameric configuration. Using a Cell-ELISA, we demonstrated the ability of the immune serum to detect Kv2.1 channels on the surface of cells that express the channel. Then, using a Patch Clamp electrophysiology assay we explored the capability of the dromedary serum in modulating Kv2.1 currents. Cells that were incubated for 3h with serum taken at Day 51 from the start of the immunization displayed a statistically significant 2-fold reduction in current density compared to control conditions as well as cells incubated with serum from Day 0. Here we show that an immunization approach with cells overexpressing the Kv2.1 channel yields immune serum with Kv2.1 specific antibodies.
电压门控钾(Kv)通道构成细胞的复极化能力,通常在可兴奋细胞中表达。在非可兴奋细胞中,诸如Kv2.1之类的Kv通道参与细胞分化和生长。由于Kv2.1参与多种生理过程,这些通道是很有前景的治疗靶点。为了开发基于Kv2.1特异性抗体的通道调节剂,我们采用了一种新方法,用过量表达小鼠Kv2.1通道的异源Ltk-细胞免疫单峰骆驼,而不是用通道蛋白片段进行免疫。这种方法的优点是通道以其天然四聚体构象呈现。使用细胞酶联免疫吸附测定法,我们证明了免疫血清能够检测表达该通道的细胞表面上的Kv2.1通道。然后,使用膜片钳电生理测定法,我们探究了单峰骆驼血清调节Kv2.1电流的能力。与对照条件以及用第0天的血清孵育的细胞相比,用免疫开始后第51天采集的血清孵育3小时的细胞,其电流密度在统计学上显著降低了2倍。在此我们表明,用过量表达Kv2.1通道的细胞进行免疫的方法可产生具有Kv2.1特异性抗体的免疫血清。