Different KChIPs Compete for Heteromultimeric Assembly with Pore-Forming Kv4 Subunits

• Published in: Biophysical journal 2015-06, Vol.108 (11), p.2658-2669
• Main Authors: Zhou, Jingheng, Tang, Yiquan, Zheng, Qin, Li, Meng, Yuan, Tianyi, Chen, Liangyi, Huang, Zhuo, Wang, KeWei
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Binding sites; Binding, Competitive; Biochemistry; Biophysics; Channels and Transporters; Gene Expression Regulation; HEK293 Cells; Humans; Ion Channel Gating; Kinetics; Kv Channel-Interacting Proteins - chemistry; Kv Channel-Interacting Proteins - metabolism; Microscopy; Neuropsychology; Peptides; Porosity; Protein Multimerization; Protein Subunits - chemistry; Protein Subunits - metabolism; Proteins; Shal Potassium Channels - chemistry; Shal Potassium Channels - metabolism; Xenopus
• ISSN: 0006-3495; 1542-0086
• DOI: 10.1016/j.bpj.2015.04.024

Auxiliary Kv channel-interacting proteins 1–4 (KChIPs1–4) coassemble with pore-forming Kv4 α-subunits to form channel complexes underlying somatodendritic subthreshold A-type current that regulates neuronal excitability. It has been hypothesized that different KChIPs can competitively bind to Kv4 α-subunit to form variable channel complexes that can exhibit distinct biophysical properties for modulation of neural function. In this study, we use single-molecule subunit counting by total internal reflection fluorescence microscopy in combinations with electrophysiology and biochemistry to investigate whether different isoforms of auxiliary KChIPs, KChIP4a, and KChIP4bl, can compete for binding of Kv4.3 to coassemble heteromultimeric channel complexes for modulation of channel function. To count the number of photobleaching steps solely from cell membrane, we take advantage of a membrane tethered k-ras-CAAX peptide that anchors cytosolic KChIP4 proteins to the surface for reduction of background noise. Single-molecule subunit counting reveals that the number of KChIP4 isoforms in Kv4.3-KChIP4 complexes can vary depending on the KChIP4 expression level. Increasing the amount of KChIP4bl gradually reduces bleaching steps of KChIP4a isoform proteins, and vice versa. Further analysis of channel gating kinetics from different Kv4-KChIP4 subunit compositions confirms that both KChIP4a and KChIP4bl can modulate the channel complex function upon coassembly. Taken together, our findings show that auxiliary KChIPs can heteroassemble with Kv4 in a competitive manner to form heteromultimeric Kv4-KChIP4 channel complexes that are biophysically distinct and regulated under physiological or pathological conditions.