Takagi T, Petrova T, Comte M, Kuster T, Heizmann C W, Cox J A
Biological Institute, Faculty of Science, Tohoku University, Sendai, Japan.
Eur J Biochem. 1994 Apr 1;221(1):537-46. doi: 10.1111/j.1432-1033.1994.tb18766.x.
Troponin C (TnC) from amphioxus (Protochordate) was purified and its primary structure determined. Unlike the case of vertebrates and other invertebrates, amphioxus TnC is found in the soluble fraction after extractions at physiological ionic strength in the presence of Ca2+. Edman sequencing combined with mass spectroscopy indicate that the protein contains 163 amino acid residues. It possesses an acetylated N-terminus (although a small percentage has a free Ser N-terminus) and either epsilon-N-methyllysine or epsilon-N-dimethyllysine in position 20. It displays about 50% sequence identity with vertebrate skeletal-muscle and cardiac-muscle TnC, 44% with TnC of sea squirt, also a Protochordate, and 30% with other invertebrate TnC. Like vertebrate TnC, amphioxus TnC contains a N-terminal alpha-helix plus the usual four ancestral Ca(2+)-binding regions, but analysis of the sequence suggests that the fourth site is not functional. Flow dialysis shows that amphioxus TnC binds three Ca2+ with the mean apparent affinity constant K' of 3.4 +/- 1.5 10(5) M-1. No cooperativity exists between the sites, and the presence of up to 10 mM Mg2+ does not influence the Ca(2+)-binding isotherm, indicating that the metal-binding sites are Ca(2+)-specific at physiological Mg2+ concentrations. It forms a Ca(2+)-dependent, 1:1 complex with melittin and rabbit or crayfish troponin I (TnI). Amphioxus TnC possesses one Trp residue in position 151 and one at the C-terminus. Trp fluorescence suggests that one or both residues are solvent-exposed in the metal-free form and efficiently shielded in the Ca2+ form. Although Mg2+ has no effect on the Ca2+ binding, the Trp fluorescence is influenced by millimolar Mg2+, suggesting the presence of one or more independent Mg(2+)-binding site(s). A phylogenetic analysis clearly shows that amphioxus TnC is positioned on the branch of the Chordates, but at a distance from the vertebrate TnC. Its place on the phylogenetic tree is in accordance with the consensus evolutionary phylogeny.
文昌鱼(原索动物)的肌钙蛋白C(TnC)被纯化并确定了其一级结构。与脊椎动物和其他无脊椎动物的情况不同,在生理离子强度下于Ca2+存在时进行提取后,文昌鱼TnC存在于可溶部分。埃德曼测序结合质谱分析表明该蛋白质含有163个氨基酸残基。它具有乙酰化的N端(尽管一小部分具有游离的丝氨酸N端),并且在第20位含有ε-N-甲基赖氨酸或ε-N-二甲基赖氨酸。它与脊椎动物骨骼肌和心肌TnC的序列同一性约为50%,与同样是原索动物的海鞘的TnC序列同一性为44%,与其他无脊椎动物TnC的序列同一性为30%。与脊椎动物TnC一样,文昌鱼TnC包含一个N端α-螺旋以及通常的四个原始Ca(2+)结合区域,但序列分析表明第四个位点没有功能。流动透析显示文昌鱼TnC结合三个Ca2+,平均表观亲和常数K'为3.4±1.5×10(5) M-1。位点之间不存在协同性,高达10 mM的Mg2+的存在不影响Ca(2+)结合等温线,表明在生理Mg2+浓度下金属结合位点对Ca(2+)具有特异性。它与蜂毒肽以及兔或小龙虾肌钙蛋白I(TnI)形成Ca(2+)依赖性的1:1复合物。文昌鱼TnC在第151位和C端各有一个色氨酸残基。色氨酸荧光表明一个或两个残基在无金属形式下暴露于溶剂中,而在Ca2+形式下被有效屏蔽。尽管Mg2+对Ca2+结合没有影响,但毫摩尔浓度的Mg2+会影响色氨酸荧光,表明存在一个或多个独立的Mg(2+)结合位点。系统发育分析清楚地表明文昌鱼TnC位于脊索动物分支上,但与脊椎动物TnC有一定距离。它在系统发育树上的位置与公认的进化系统发育一致。