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The AHNAKs are a class of giant propeller-like proteins that associate with calcium channel proteins of cardiomyocytes and other cells

机译:AHNAK是一类巨大的螺旋桨状蛋白,与心肌细胞和其他细胞的钙通道蛋白相关

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摘要

To explore the function of the giant AHNAK molecule, first described in 1992 [Shtivelman, E., Cohen, F. E. & Bishop, J. M. (1992) Proc. Natl. Acad. Sci. USA 89, 5472–5476], we created AHNAK null mice by homologous recombination. Homozygous knockouts showed no obvious phenotype, but revealed instead a second AHNAK-like molecule, provisionally designated AHNAK2. Like the original AHNAK, AHNAK2 is a 600-kDa protein composed of a large number of highly conserved repeat segments. Structural predictions suggest that the repeat segments of both AHNAKs may have as their basic framework a series of linked, antiparallel β-strands similar to those found in β-propeller proteins. Both AHNAKs appear to localize to Z-band regions of mouse cardiomyocytes and cosediment with membrane vesicles containing the dihydropyridine receptor, which is consistent with earlier reports that the AHNAKs are linked to L-type calcium channels and can be phosphorylated by protein kinase A. The localization of the AHNAKs in close proximity to transverse tubule membranes and Z-band regions of cardiac sarcomeres raise the possibility that they might be involved in regulating excitation/contraction coupling of cardiomyocytes, but other studies indicate that the association of AHNAKs with calcium channel proteins is more widespread. AHNAK2 is predicted to have a PDZ domain within its N-terminal, nonrepeating domain, which may mediate these interactions.
机译:为了探索巨型AHNAK分子的功能,最早于1992年进行了描述[Shtivelman,E.,Cohen,F. E.&Bishop,J.M.(1992)Proc.Natl.Acad.Sci.USA 90:5873-5877。 Natl。学院科学[USA 89,5472-5476],我们通过同源重组创建了AHNAK null小鼠。纯合子敲除没有显示明显的表型,而是揭示了第二个类似AHNAK的分子,临时命名为AHNAK2。像原始的AHNAK一样,AHNAK2是一个600 kDa的蛋白质,由大量高度保守的重复片段组成。结构预测表明,两个AHNAK的重复片段都可能具有一系列与β-螺旋桨蛋白相似的,相互连接的反平行β链作为其基本框架。两种AHNAK似乎都定位于小鼠心肌细胞的Z带区域,并与含有二氢吡啶受体的膜囊泡共沉淀,这与早期的报道一致,即AHNAK与L型钙通道相连并且可以被蛋白激酶A磷酸化。 AHNAKs定位于心肌肉瘤的小管横膜和Z带区域附近,这增加了它们可能参与调节心肌细胞的兴奋/收缩偶联的可能性,但其他研究表明AHNAKs与钙通道蛋白的相关性是更普遍。预计AHNAK2在其N末端非重复域中具有PDZ域,该域可能介导这些相互作用。

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