Linder Jürgen Ulrich
Department of Biochemistry, University of Bayreuth, Bayreuth, Germany.
PLoS One. 2015 Oct 29;10(10):e0141843. doi: 10.1371/journal.pone.0141843. eCollection 2015.
YHS-domains are small protein modules which have been proposed to bind transition-metal ions like the related TRASH-domains. They are found in a variety of enzymes including copper-transporting ATPases and adenylyl cyclases. Here we investigate a class IIIc adenylyl cyclase from Mycobacterium phlei which contains a C-terminal YHS-domain linked to the catalytic domain by a peptide of 8 amino acids. We expressed the isolated catalytic domain and the full-length enzyme in E. coli. The catalytic domain requires millimolar Mn2+ as a cofactor for efficient production of cAMP, is unaffected by low micromolar concentrations of Cu2+ and inhibited by concentrations higher than 10 μM. The full-length enzyme also requires Mn2+ in the absence of an activator. However, 1-10 μM Cu2+ stimulate the M. phlei adenylyl cyclase sixfold when assayed with Mn2+. With Mg2+ as the probable physiological cofactor of the adenylyl cyclase Cu2+ specifically switches the enzyme from an inactive to an active state. Other transition-metal ions do not elicit activity with Mg2+. We favor the view that the YHS-domain of M. phlei adenylyl cyclase acts as a sensor for copper ions and signals elevated levels of the transition-metal via cAMP. By analogy to TRASH-domains binding of Cu2+ probably occurs via one conserved aspartate and three conserved cysteine-residues in the YHS-domain.
YHS结构域是一种小的蛋白质模块,有人提出它能像相关的TRASH结构域一样结合过渡金属离子。它们存在于多种酶中,包括铜转运ATP酶和腺苷酸环化酶。在这里,我们研究了来自草分枝杆菌的IIIc类腺苷酸环化酶,它含有一个C端YHS结构域,通过一个8个氨基酸的肽段与催化结构域相连。我们在大肠杆菌中表达了分离的催化结构域和全长酶。催化结构域需要毫摩尔浓度的Mn2+作为辅因子才能高效产生cAMP,不受低微摩尔浓度Cu2+的影响,但会被高于10μM的浓度抑制。在没有激活剂的情况下,全长酶也需要Mn2+。然而,在用Mn2+进行测定时,1 - 10μM的Cu2+能将草分枝杆菌腺苷酸环化酶的活性提高6倍。以Mg2+作为腺苷酸环化酶可能的生理辅因子时,Cu2+能特异性地将该酶从无活性状态转变为活性状态。其他过渡金属离子不会引发该酶与Mg2+相关的活性。我们倾向于这样一种观点,即草分枝杆菌腺苷酸环化酶的YHS结构域作为铜离子的传感器,通过cAMP信号传导过渡金属水平的升高。类似于TRASH结构域,Cu2+的结合可能通过YHS结构域中一个保守的天冬氨酸和三个保守的半胱氨酸残基发生。