Fan Zhuo, Zhang Zhenggang, Fu Mingyu, Qi Zhi, Xiao Zhongju
Department of Physiology, Southern Medical University, Guangzhou, China.
Biochim Biophys Acta. 2013 Mar;1828(3):990-6. doi: 10.1016/j.bbamem.2012.11.016. Epub 2012 Nov 27.
Rapid inactivation of voltage-gated potassium channel plays an important role in shaping the electrical signaling in neurons and other excitable cells. N-type ("ball and chain") inactivation, as the most extensively studied inactivation model, is assumed to be the inactivation mechanism of Kv1.4 channel. The inactivation ball inactivates the channel by interacting with the hydrophobic wall of inner pore and occluding it. Recently, we have proved that the electrostatic interaction between two charged segments in the NH(2)-termainal plays an important role through promoting the inactivation process of the Kv1.4 channel. This study investigates the effect of inserting negatively or positively charged short peptides at NH(2)-terminal on the inactivation of Kv1.4 channel. The results that inserting negatively-charged peptide (either myc or D-peptide) at different sites of NH(2)-terminal, deceleraes inactivation process of Kv1.4 channel to a different extent with inserting site changing and that the mutant Kv1.4-D50 exhibits a more slower inactivation rate than Kv1.4-K50 further identified the role of electrostatic interactions in the "ball and chain" inactivation mechanism.
电压门控钾通道的快速失活在塑造神经元和其他可兴奋细胞的电信号传导中起着重要作用。N型(“球链”)失活作为研究最广泛的失活模型,被认为是Kv1.4通道的失活机制。失活球通过与内孔的疏水壁相互作用并将其堵塞来使通道失活。最近,我们已经证明,NH(2)末端两个带电荷片段之间的静电相互作用通过促进Kv1.4通道的失活过程发挥重要作用。本研究调查了在NH(2)末端插入带负电荷或正电荷的短肽对Kv1.4通道失活的影响。在NH(2)末端不同位点插入带负电荷肽(myc或D肽),随着插入位点的变化,Kv1.4通道的失活过程在不同程度上减慢,并且突变体Kv1.4-D50比Kv1.4-K50表现出更慢的失活速率,这进一步证实了静电相互作用在“球链”失活机制中的作用。