Hua Wei, Liang Shuping, Lu Ying-Tang
Key Lab of MOE for Plant Developmental Biology, College of Life Sciences, Wuhan University, Wuhan 430072, People's Republic of China.
Biochem J. 2003 Nov 15;376(Pt 1):291-302. doi: 10.1042/BJ20030736.
A calcium (Ca2+)/calmodulin (CaM)-binding protein kinase (CBK) from tobacco (Nicotiana tabaccum ), NtCBK2, has been characterized molecularly and biochemically. NtCBK2 has all 11 conserved subdomains of the kinase-catalytic domain and a CaM-binding site as shown by other kinases, including Ca2+-dependent protein kinase and chimaeric Ca2+/CaM-dependent protein kinases. However, this kinase does not contain an EF-hand motif for Ca2+ binding, and its activity was not regulated by Ca2+. Whereas NtCBK2 phosphorylated both itself and other substrates, such as histone IIIS and syntide-2, in a Ca2+/CaM-independent manner, as also shown by OsCBK, a CaM-binding protein kinase from rice (Oryza sativa ), the kinase activity of NtCBK2 was greatly stimulated by Ca2+/CaM, whereas that of OsCBK was not. By molecular dissection analyses, the CaM-binding domain of NtCBK2 has been localized in a stretch of 30 amino acid residues at residue positions 431-460 as a 1-5-10 protein motif. Three tobacco CaM isoforms (NtCaM1, NtCaM3 and NtCaM13) used in the present study have been shown to bind to NtCBK2, but with different dissociation constants ( K(d)s), as follows: NtCaM1, 55.7 nM; NtCaM3, 25.4 nM; and NtCaM13, 19.8 nM, indicating that NtCBK2 has a higher affinity for NtCaM3 and NtCaM13 than for NtCaM1. The enzymic activity of NtCBK2 was also modulated differently by various CaM isoforms. Whereas the phosphorylation activity of NtCBK2 was shown by assay to be enhanced only approximately 2-3-fold by the presence of NtCaM1, the activity could be amplified up to 8-9-fold by NtCaM3 or 10-11-fold by NtCaM13, suggesting that NtCaM3 and NtCaM13 are better activators than NtCaM1 for NtCBK2.
已从烟草(烟草属)中对一种钙(Ca2+)/钙调蛋白(CaM)结合蛋白激酶(CBK)——NtCBK2进行了分子和生化特性分析。NtCBK2具有激酶催化结构域的所有11个保守亚结构域以及一个CaM结合位点,其他激酶如钙依赖蛋白激酶和嵌合型Ca2+/CaM依赖蛋白激酶也有这些结构域。然而,这种激酶不含用于Ca2+结合的EF手基序,其活性不受Ca2+调节。虽然NtCBK2能以不依赖Ca2+/CaM的方式使自身和其他底物(如组蛋白IIIS和合成肽-2)磷酸化,水稻(稻属)的一种CaM结合蛋白激酶OsCBK也有此现象,但NtCBK2的激酶活性受到Ca2+/CaM的极大刺激,而OsCBK的激酶活性则不受其刺激。通过分子剖析分析,NtCBK2的CaM结合结构域已定位在第431 - 460位残基的一段30个氨基酸残基中,呈1 - 5 - 10蛋白基序。本研究中使用的三种烟草CaM同工型(NtCaM1、NtCaM3和NtCaM13)已被证明能与NtCBK2结合,但解离常数(K(d)s)不同,如下:NtCaM1为55.7 nM;NtCaM3为25.4 nM;NtCaM13为19.8 nM,这表明NtCBK2对NtCaM3和NtCaM13的亲和力高于对NtCaM1的亲和力。NtCBK2的酶活性也受到不同CaM同工型的不同调节。通过测定表明,NtCaM1的存在仅使NtCBK2的磷酸化活性增强约2 - 3倍,而NtCaM3可使其活性放大至8 - 9倍,NtCaM13可使其活性放大至10 - (此处原文有误,推测应为10 - 11倍),这表明对于NtCBK2而言,NtCaM3和NtCaM13比NtCaM1是更好的激活剂。