Huang Shyh-Shyun, Deng Jeng-Shyan, Chen Hsien-Jung, Lin Yaw-Huei, Huang Guan-Jhong
Department of Pharmacy, College of Pharmacy, China Medical University, Taichung, 404, Taiwan.
Department of Health and Nutrition Biotechnology, Asia University, Taichung, 413, Taiwan.
Bot Stud. 2014 Dec;55(1):64. doi: 10.1186/s40529-014-0064-4. Epub 2014 Aug 15.
Metallothionein (MT) characterized by their low molecular weight and high cysteine content.
Two recombinant proteins of MT-I and MT-II overproduced in E. coli (M15) was purified by Ni-chelated affinity chromatography. The molecular mass of MT-I and MT-II are ca. 6,600 and 8,000 Da as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Total antioxidant status, DPPH radical scavenging activity, reducing power method, Fe-chelating ability, ferric thiocyanate (FTC) method, and protecting calf thymus DNA against hydroxyl radical-induced damage were studied. The MT-I and MT-II proteins with a concentration of 100 μg/mL exhibited the highest activity (expressed respectively as 61.72 ± 0.13 and 74.28 ± 1.15 μM Trolox equivalent antioxidative capacity, TEAC) in total antioxidant status test. Like total antioxidant status, DPPH radical scavenging activity, reducing power, Fe-chelating ability, FTC activity, and protecting calf thymus DNA against hydroxyl radical-induced damage all showed that MT-1 and MT-II proteins have antioxidant activities. In this study, we also found that antioxidant activities of MT-I and MT-II increased from 17% and 16% (0 h) to about 26% and 28% (24 h) after 24 h hydrolysis by trypsin. Smaller peptides increased the antioxidant activities. Four and three peptides, respectively, from MT-I and MT-II protein sequences for testing antioxidative activity were synthesized according to tryptic hydrolysis simulation. The obtained MSSGCK, CGSDCK, LTLEGSSEK, ATEGGHACK, CGNGCGGCK, and CDPCNCK showed IC values of 309.87, 1423.37, 3925.54, 561.32, 300.76, and 610.12 μM, respectively, when scavenging activity of DPPH radicals (%) was measured.
These findings mean that a cysteine residue is most important in antiradical activities. It was suggested that MT-I and MT-II might contribute their antioxidant activities against hydroxyl and peroxyl radicals.
金属硫蛋白(MT)具有低分子量和高半胱氨酸含量的特点。
通过镍螯合亲和层析法纯化了在大肠杆菌(M15)中过量表达的两种重组蛋白MT-I和MT-II。经十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)测定,MT-I和MT-II的分子量分别约为6600和8000道尔顿。研究了总抗氧化状态、DPPH自由基清除活性、还原能力法、铁螯合能力、硫氰酸铁(FTC)法以及保护小牛胸腺DNA免受羟基自由基诱导损伤的情况。在总抗氧化状态测试中,浓度为100μg/mL的MT-I和MT-II蛋白表现出最高活性(分别表示为61.72±0.13和74.28±1.15μM Trolox等效抗氧化能力,TEAC)。与总抗氧化状态一样,DPPH自由基清除活性、还原能力、铁螯合能力、FTC活性以及保护小牛胸腺DNA免受羟基自由基诱导损伤均表明MT-1和MT-II蛋白具有抗氧化活性。在本研究中,我们还发现,经胰蛋白酶水解24小时后,MT-I和MT-II的抗氧化活性从17%和16%(0小时)增加到约26%和28%(24小时)。较小的肽增加了抗氧化活性。根据胰蛋白酶水解模拟,分别从MT-I和MT-II蛋白序列中合成了四个和三个用于测试抗氧化活性的肽。在测定DPPH自由基清除活性(%)时,得到的MSSGCK、CGSDCK、LTLEGSSEK、ATEGGHACK、CGNGCGGCK和CDPCNCK的IC值分别为309.87、1423.37、3925.54、561.32、300.76和610.12μM。
这些发现意味着半胱氨酸残基在抗自由基活性中最为重要。提示MT-I和MT-II可能对羟基自由基和过氧自由基具有抗氧化活性。