Rizzello Antonia, Ciardiello M Antonietta, Acierno Raffaele, Carratore Vito, Verri Tiziano, di Prisco Guido, Storelli Carlo, Maffia Michele
Laboratory of General Physiology, Department of Biological and Environmental Science and Technology, University of Salento, via Monteroni, 73100, Lecce, Italy.
Protein J. 2007 Aug;26(5):335-48. doi: 10.1007/s10930-007-9076-1.
Gill cytoplasmic carbonic anhydrase of the haemoglobinless Antarctic icefish Chionodraco hamatus (Ice-CA) was directly sequenced and consists in 259 residues with an acetylated N-terminus. The molecular mass, deduced from the sequence, was 28.45 kDa, while mass spectrometry analysis of the native protein gave higher values. Treatment with dithiothreitol abolished this difference, indicating possible post-translational modifications. Isoelectric focusing analysis of Ice-CA suggested S-thiolation, which was identified as S-glutathionylation by immunostaining. Deglutathionylated Ice-CA maintained the anhydrase activity but showed higher susceptibility to hydrogen peroxide, suggesting that glutathione binding to Cys residues may have a role in the defence against oxidative damage. Ice-CA is characterized by lower thermal stability, higher activity and lower activation energy than its homologue gill CA of the temperate European eel, confirming the adaptation of the catalytic capacity to low temperatures. Alignment of Ice-CA with homologous enzymes from other fish shows high identity; the enzyme is grouped with a previously described fish CA monophyletic clade although Ice-CA shows several characteristics that can increase protein-solvent interaction and structural flexibility.
对无血红蛋白的南极冰鱼长鳍南极鱼(Chionodraco hamatus)的鳃细胞质碳酸酐酶(冰鱼碳酸酐酶,Ice-CA)进行了直接测序,它由259个残基组成,N端乙酰化。根据序列推导,其分子量为28.45 kDa,而对天然蛋白的质谱分析得出的值更高。用二硫苏糖醇处理消除了这种差异,表明可能存在翻译后修饰。对Ice-CA的等电聚焦分析表明存在S-硫醇化,通过免疫染色鉴定为S-谷胱甘肽化。去谷胱甘肽化的Ice-CA保持了碳酸酐酶活性,但对过氧化氢的敏感性更高,这表明谷胱甘肽与半胱氨酸残基的结合可能在防御氧化损伤中起作用。与温带欧洲鳗鲡的同源鳃碳酸酐酶相比,Ice-CA的特点是热稳定性较低、活性较高和活化能较低,这证实了催化能力对低温的适应性。Ice-CA与其他鱼类的同源酶比对显示出高度同源性;该酶与先前描述的鱼类碳酸酐酶单系分支归为一类,尽管Ice-CA表现出一些可以增加蛋白质与溶剂相互作用和结构灵活性的特征。