McManus Edward, Luisi Ben F, Perham Richard N
Department of Biochemistry, University of Cambridge, Old Addenbrooke's Site, Sanger Building, 80 Tennis Court Road, Cambridge CB2 1GA, UK.
J Mol Biol. 2006 Feb 24;356(3):625-37. doi: 10.1016/j.jmb.2005.11.057. Epub 2005 Dec 5.
Lipoyl-lysine swinging arms are crucial to the reactions catalysed by the 2-oxo acid dehydrogenase multienzyme complexes. A gene encoding a putative lipoate protein ligase (LplA) of Thermoplasma acidophilum was cloned and expressed in Escherichia coli. The recombinant protein, a monomer of molecular mass 29 kDa, was catalytically inactive. Crystal structures in the absence and presence of bound lipoic acid were solved at 2.1 A resolution. The protein was found to fall into the alpha/beta class and to be structurally homologous to the catalytic domains of class II aminoacyl-tRNA synthases and biotin protein ligase, BirA. Lipoic acid in LplA was bound in the same position as biotin in BirA. The structure of the T.acidophilum LplA and limited proteolysis of E.coli LplA together highlighted some key features of the post-translational modification. A loop comprising residues 71-79 in the T.acidophilum ligase is proposed as interacting with the dithiolane ring of lipoic acid and discriminating against the entry of biotin. A second loop comprising residues 179-193 was disordered in the T.acidophilum structure; tryptic cleavage of the corresponding loop in the E.coli LplA under non-denaturing conditions rendered the enzyme catalytically inactive, emphasizing its importance. The putative LplA of T.acidophilum lacks a C-terminal domain found in its counterparts in E.coli (Gram-negative) or Streptococcus pneumoniae (Gram-positive). A gene encoding a protein that appears to have structural homology to the additional domain in the E.coli and S.pneumoniae enzymes was detected alongside the structural gene encoding the putative LplA in the T.acidophilum genome. It is likely that this protein is required to confer activity on the LplA as currently purified, one protein perhaps catalysing the formation of the obligatory lipoyl-AMP intermediate, and the other transferring the lipoyl group from it to the specific lysine residue in the target protein.
硫辛酰赖氨酸摆动臂对于2-氧代酸脱氢酶多酶复合物催化的反应至关重要。克隆了嗜热栖热菌中一个编码假定硫辛酸蛋白连接酶(LplA)的基因,并在大肠杆菌中进行表达。重组蛋白为分子量29 kDa的单体,无催化活性。在有无结合硫辛酸的情况下,以2.1 Å的分辨率解析了晶体结构。发现该蛋白属于α/β类,在结构上与II类氨酰-tRNA合成酶和生物素蛋白连接酶BirA的催化结构域同源。LplA中的硫辛酸结合位置与BirA中的生物素相同。嗜热栖热菌LplA的结构以及大肠杆菌LplA的有限蛋白酶解共同突出了翻译后修饰的一些关键特征。提出嗜热栖热菌连接酶中包含71 - 79位残基的环与硫辛酸的二硫戊环相互作用,并区分生物素的进入。在嗜热栖热菌结构中,包含179 - 193位残基的第二个环无序;在非变性条件下,大肠杆菌LplA中相应环的胰蛋白酶切割使该酶无催化活性,强调了其重要性。嗜热栖热菌的假定LplA缺乏在大肠杆菌(革兰氏阴性菌)或肺炎链球菌(革兰氏阳性菌)对应物中发现的C末端结构域。在嗜热栖热菌基因组中,与编码假定LplA的结构基因一起检测到一个编码与大肠杆菌和肺炎链球菌酶中的附加结构域具有结构同源性的蛋白的基因。目前纯化的LplA可能需要这种蛋白来赋予其活性,一种蛋白可能催化必需的硫辛酰-AMP中间体的形成,另一种蛋白则将硫辛酰基团从该中间体转移到靶蛋白中的特定赖氨酸残基上。