Adams Julian, Chen Zhi-Ping, Van Denderen Bryce J W, Morton Craig J, Parker Michael W, Witters Lee A, Stapleton David, Kemp Bruce E
St. Vincent's Institute of Medical Research, Fitzroy, Victoria 3065, Australia.
Protein Sci. 2004 Jan;13(1):155-65. doi: 10.1110/ps.03340004.
AMP-activated protein kinase (AMPK) is a alphabetagamma heterotrimer that is activated in response to both hormones and intracellular metabolic stress signals. AMPK is regulated by phosphorylation on the alpha subunit and by AMP allosteric control previously thought to be mediated by both alpha and gamma subunits. Here we present evidence that adjacent gamma subunit pairs of CBS repeat sequences (after Cystathionine Beta Synthase) form an AMP binding site related to, but distinct from the classical AMP binding site in phosphorylase, that can also bind ATP. The AMP binding site of the gamma(1) CBS1/CBS2 pair, modeled on the structures of the CBS sequences present in the inosine monophosphate dehydrogenase crystal structure, contains three arginine residues 70, 152, and 171 and His151. The yeast gamma homolog, snf4 contains a His151Gly substitution, and when this is introduced into gamma(1), AMP allosteric control is substantially lost and explains why the yeast snf1p/snf4p complex is insensitive to AMP. Arg70 in gamma(1) corresponds to the site of mutation in human gamma(2) and pig gamma(3) genes previously identified to cause an unusual cardiac phenotype and glycogen storage disease, respectively. Mutation of any of AMP binding site Arg residues to Gln substantially abolishes AMP allosteric control in expressed AMPK holoenzyme. The Arg/Gln mutations also suppress the previously described inhibitory properties of ATP and render the enzyme constitutively active. We propose that ATP acts as an intrasteric inhibitor by bridging the alpha and gamma subunits and that AMP functions to derepress AMPK activity.
AMP激活的蛋白激酶(AMPK)是一种αβγ异源三聚体,可响应激素和细胞内代谢应激信号而被激活。AMPK受α亚基上的磷酸化调节,并受AMP变构控制,此前认为这种变构控制由α和γ亚基共同介导。在此,我们提供证据表明,CBS重复序列(在胱硫醚β合酶之后)的相邻γ亚基对形成了一个与磷酸化酶中的经典AMP结合位点相关但不同的AMP结合位点,该位点也能结合ATP。基于肌苷单磷酸脱氢酶晶体结构中存在的CBS序列结构构建的γ(1) CBS1/CBS2对的AMP结合位点,包含三个精氨酸残基70、152和171以及His151。酵母γ同源物snf4含有His151Gly替代,当将其引入γ(1)时,AMP变构控制基本丧失,这解释了酵母snf1p/snf4p复合物对AMP不敏感的原因。γ(1)中的Arg70对应于人类γ(2)和猪γ(3)基因中先前分别被鉴定为导致异常心脏表型和糖原贮积病的突变位点。将AMP结合位点的任何一个精氨酸残基突变为谷氨酰胺,在表达的AMPK全酶中基本消除了AMP变构控制。Arg/Gln突变也抑制了先前描述的ATP的抑制特性,并使该酶组成型激活。我们提出,ATP通过连接α和γ亚基而作为一种内源性抑制剂起作用,而AMP则起到解除对AMPK活性抑制的作用。