Department of Cell Biology, University ofOklahoma Health Sciences Center, 940 Stanton L. Young Boulevard, Oklahoma City, Oklahoma 73104, USA.
Biochemistry. 2010 Mar 2;49(8):1628-39. doi: 10.1021/bi901960u.
The cone photoreceptor cyclic nucleotide-gated (CNG) channel plays a pivotal role in phototransducton. Mutations in the channel subunits are associated with achromatopsia and progressive cone dystrophy in humans. More than 50 mutations have been identified in the channel CNGA3 subunit, with 50% of them located in the carboxyl (C) terminus. This study investigates the defects of the two frequently occurring mutations, R377W and F488L, in the C-terminus of CNGA3. Ratiometric measurement of the intracellular Ca(2+) concentration and electrophysiological recordings showed the loss of functional activity of the mutant channels in an HEK293 heterologous expression system. Immunofluorescence labeling revealed an apparent cytosolic aggregation of the mutant channels compared to the wild type (WT). The R377W and F488L mutants, expressed and purified from Escherichia coli as glutathione S-transferase (GST) fused to the CNGA3 C-terminal domain, showed no negative effects on interactions with the channel subunits. Circular dichroism spectrum analyses were performed to examine the structural impact of the mutations. Although the R377W and F488L C-termini mutants retained stable, folded structures, the secondary structures of both mutants differed from the WT protein. Furthermore, the WT C-terminus exhibited a significant decrease in alpha-helical content in response to the channel ligands, while this allosteric transition was diminished in the two mutants. This is the first study showing the structural impact of the disease-causing mutations in the cone CNG channel subunit. The observed alterations in the local secondary structure and active conformational change may confer an adverse effect on the channel's activity and cellular processing.
视锥细胞环核苷酸门控(CNG)通道在光转导中起着关键作用。通道亚基的突变与人类的色盲和进行性锥体细胞营养不良有关。在通道 CNGA3 亚基中已经发现了超过 50 种突变,其中 50%位于羧基(C)末端。本研究探讨了 CNGA3 羧基末端两个常见突变 R377W 和 F488L 的缺陷。细胞内 Ca(2+)浓度的比率测量和电生理记录显示,突变通道在 HEK293 异源表达系统中的功能活性丧失。免疫荧光标记显示突变通道与野生型(WT)相比明显在细胞质中聚集。与野生型相比,从大肠杆菌表达和纯化的作为谷胱甘肽 S-转移酶(GST)融合到 CNGA3 C 末端结构域的 R377W 和 F488L 突变体,对与通道亚基的相互作用没有负面影响。圆二色光谱分析用于检查突变对结构的影响。尽管 R377W 和 F488L C 末端突变体保留了稳定的折叠结构,但两种突变体的二级结构均与 WT 蛋白不同。此外,WT C 末端在通道配体的作用下表现出明显的α-螺旋含量减少,而这种变构转变在两个突变体中减弱。这是首次研究表明视锥细胞 CNG 通道亚基的致病突变对结构的影响。观察到的局部二级结构和活性构象变化的改变可能对通道的活性和细胞处理产生不利影响。