Action potentials are initiated and modulated at the axon initial segment (AIS) by highly clustered ion channels. Voltage-gated Kv1 potassium channels underlie most outward AIS K(+) current. AIS Kv1 channels exist in a large protein complex including ADAM22, Caspr2, and LGI1. However, their clustering mechanisms remain unknown. Because Kv1 channels have a highly conserved PDZ-binding motif, we used CRISPR-based genome editing to screen 18 PDZ domain-containing proteins identified in our previous AIS proximity proteome for their AIS localization. Among these, we found that the scaffolding proteins SCRIB and PSD93 are highly enriched at the AIS. Using CRISPR-mediated knockout, cell surface clustering assays, and coimmunoprecipitation, we show that SCRIB and PSD93 bind to and are required for AIS Kv1 channel clustering, whereas SCRIB links the AIS Kv1 channel protein complex to the master AIS scaffolding protein AnkyrinG. These results define a hierarchy of scaffolding proteins that combine to cluster AIS Kv1 channels.
A hierarchy of PDZ domain scaffolding proteins clusters the Kv1 K(+) channel protein complex at the axon initial segment.
PDZ 结构域支架蛋白的层级结构将 Kv1 K(+) 通道蛋白复合物聚集在轴突起始段
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作者:Zhang Wei, Palfini Victoria L, Wu Yu, Ding Xiaoyun, Melton Allison J, Gao Yudong, Ogawa Yuki, Rasband Matthew N
| 期刊: | Science Advances | 影响因子: | 12.500 |
| 时间: | 2025 | 起止号: | 2025 May 23; 11(21):eadv1281 |
| doi: | 10.1126/sciadv.adv1281 | 研究方向: | 其它 |
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