首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Cyclic Nucleotide-gated Channel α-3 (CNGA3) Interacts with Stereocilia Tip-Link Cadherin 23 + Exon 68 or Alternatively with Myosin VIIa Two Proteins Required for Hair Cell Mechanotransduction
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Cyclic Nucleotide-gated Channel α-3 (CNGA3) Interacts with Stereocilia Tip-Link Cadherin 23 + Exon 68 or Alternatively with Myosin VIIa Two Proteins Required for Hair Cell Mechanotransduction

机译:环状核苷酸门控通道α-3(CNGA3)与Stereocilia Tip-Link钙黏着蛋白23 +外显子68相互作用或与肌球蛋白VIIa相互作用这是毛细胞机械转导所需的两种蛋白质

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摘要

Previously, we obtained evidence for a photoreceptor/olfactory type of CNGA3 transcript in a purified teleost vestibular hair cell preparation with immunolocalization of CNGA3 protein to stereocilia of teleost vestibular and mammalian cochlear hair cells. The carboxyl terminus of highly Ca2+-permeable CNGA3 expressed in the mammalian organ of Corti and saccular hair cells was found to interact with an intracellular domain of microfibril interface-located protein 1 (EMILIN 1), a member of the elastin superfamily, also immunolocalizd to hair cell stereocilia (Selvakumar, D., Drescher, M. J., Dowdall, J. R., Khan, K. M., Hatfield, J. S., Ramakrishnan, N. A., and Drescher, D. G. (2012) Biochem. J. 443, 463–476). Here, we provide evidence for organ of Corti proteins, of Ca2+-dependent binding of the amino terminus of CNGA3 specifically to the carboxyl terminus of stereocilia tip-link protein CDH23 +68 (cadherin 23 with expressed exon 68) by yeast two-hybrid mating and co-transformation protocols, pulldown assays, and surface plasmon resonance analysis. Myosin VIIa, required for adaptation of hair cell mechanotransduction (MET) channel(s), competed with CDH23 +68, with direct Ca2+-dependent binding to the amino terminus of CNGA3. Based upon the premise that hair cell stereocilia tip-link proteins are closely coupled with MET, these results are consistent with the possibility that CNGA3 participates in hair-cell MET. Together with the demonstration of protein-protein interaction between HCN1 and tip-link protein protocadherin 15 CD3 (Ramakrishnan, N. A., Drescher, M. J., Barretto, R. L., Beisel, K. W., Hatfield, J. S., and Drescher, D. G. (2009) J. Biol. Chem. 284, 3227–3238; Ramakrishnan, N. A., Drescher, M. J., Khan, K. M., Hatfield, J. S., and Drescher, D. G. (2012) J. Biol. Chem. 287, 37628–37646), a protein-protein interaction for CNGA3 and a second tip-link protein, CDH23 +68, further suggests possible association of two different channels with a single stereocilia tip link.
机译:以前,我们获得了在纯化的硬骨前庭毛细胞制备物中CNGA3转录物的感光/嗅觉类型的证据,其中CNGA3蛋白免疫定位于硬骨鱼前庭和哺乳动物的耳蜗毛细胞。发现在哺乳动物的Corti和囊性毛细胞中表达的具有高Ca 2 + 渗透性的CNGA3的羧基末端与微纤维界面定位蛋白1(EMILIN 1)的胞内结构域相互作用。弹性蛋白超家族成员,也免疫定位于毛细胞立体纤毛(Selvakumar,D.,Drescher,MJ,Dowdall,JR,Khan,KM,Hatfield,JS,Ramakrishnan,NA,and Drescher,DG(2012)Biochem.J.443 ,463–476)。在这里,我们为Corti蛋白的器官,CNGA3的氨基末端特异于纤毛纤毛末端连接蛋白CDH23 +68(钙黏着蛋白23的羧基末端)的Ca 2 + 依赖性结合提供证据外显子68)通过酵母双杂交交配和共转化协议,下拉检测和表面等离振子共振分析。适应毛细胞机械转导(MET)通道所需的肌球蛋白VIIa与CDH23 +68竞争,并直接依赖Ca 2 + 结合到CNGA3的氨基末端。基于毛细胞立体纤毛末端连接蛋白与MET紧密结合的前提,这些结果与CNGA3参与毛细胞MET的可能性一致。以及HCN1和尖端连接蛋白原钙粘蛋白15 CD3之间蛋白质相互作用的证明(Ramakrishnan,NA,Drescher,MJ,Barretto,RL,Beisel,KW,Hatfield,JS和Drescher,DG(2009)J.Biol Chem。284,3227–3238; Ramakrishnan,NA,Drescher,MJ,Khan,KM,Hatfield,JS和Drescher,DG(2012)J. Biol。Chem。287,37628–37646),蛋白质-蛋白质相互作用对于CNGA3和第二个尖端连接蛋白CDH23 +68的研究进一步表明,两个不同的通道可能与单个立体纤毛尖端连接相关联。

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