Ando S, Tokui T, Yano T, Inagaki M
Biophysics Unit and Laboratory of Biochemistry, Aichi Cancer Center Research Institite, Chikusa-ku, Nagoya, Japan.
Biochem Biophys Res Commun. 1996 Apr 5;221(1):67-71. doi: 10.1006/bbrc.1996.0546.
We reported earlier that phosphorylation in vitro of keratin filaments reconstituted from rat type I keratin 18 and type II keratin 8 by cAPM-dependent protein kinase induces disassembly of the keratin filament structure. Keratin 8 rather than keratin 18 was the major target of the kinase. We have now identified the sites on rat keratin 8 for cAMP-dependent protein kinase. Sequential analysis of the purified phosphoropeptides, together with the known primary sequence, revealed that four major sites, Ser-12, Ser-23, Ser-36, and Ser-50, and three minor sites, Ser-8, Ser-33, Ser-42, are located in the amino-terminal head domain, while three minor sites, Ser-416, Ser-423 and Ser-425 locate in the carboxyl-terminal tail domain.
我们之前报道过,由大鼠I型角蛋白18和II型角蛋白8重构的角蛋白丝在体外被cAMP依赖性蛋白激酶磷酸化会导致角蛋白丝结构的解体。角蛋白8而非角蛋白18是该激酶的主要作用靶点。我们现已确定大鼠角蛋白8上cAMP依赖性蛋白激酶的作用位点。对纯化的磷酸肽进行序列分析,并结合已知的一级序列,结果显示四个主要位点,即丝氨酸-12、丝氨酸-23、丝氨酸-36和丝氨酸-50,以及三个次要位点,丝氨酸-8、丝氨酸-33、丝氨酸-42,位于氨基末端头部结构域,而三个次要位点,丝氨酸-416、丝氨酸-423和丝氨酸-425位于羧基末端尾部结构域。