Programa de Bioquímica e Biofísica Celular, Instituto de Bioquímica Médica, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Int J Biochem Cell Biol. 2012 May;44(5):801-7. doi: 10.1016/j.biocel.2012.02.002. Epub 2012 Feb 17.
3-Bromopyruvate (3BrPA) is an antitumor agent that alkylates the thiol groups of enzymes and has been proposed as a treatment for neoplasias because of its specific reactivity with metabolic energy transducing enzymes in tumor cells. In this study, we show that the sarco/endoplasmic reticulum calcium (Ca(2+)) ATPase (SERCA) type 1 is one of the target enzymes of 3BrPA activity. Sarco/endoplasmic reticulum vesicles (SRV) were incubated in the presence of 1mM 3BrPA, which was unable to inhibit the ATPase activity of SERCA. However, Ca(2+)-uptake activity was significantly inhibited by 80% with 150 μM 3BrPA. These results indicate that 3BrPA has the ability to uncouple the ATP hydrolysis from the calcium transport activities. In addition, we observed that the inclusion of 2mM reduced glutathione (GSH) in the reaction medium with different 3BrPA concentrations promoted an increase in 40% in ATPase activity and protects the inhibition promoted by 3BrPA in calcium uptake activity. This derivatization is accompanied by a decrease of reduced cysteine (Cys), suggesting that GSH and 3BrPA increases SERCA activity and transport by pyruvylation and/or S-glutathiolation mediated by GSH at a critical Cys residues of the SERCA.
3-溴丙酮酸(3BrPA)是一种抗肿瘤剂,可使酶的巯基烷基化,由于其与肿瘤细胞中代谢能量转导酶的特异性反应,已被提议作为治疗肿瘤的方法。在这项研究中,我们表明肌浆/内质网钙(Ca(2+))ATP 酶(SERCA)1 型是 3BrPA 活性的靶酶之一。肌浆/内质网囊泡(SRV)在存在 1mM 3BrPA 的情况下孵育,3BrPA 不能抑制 SERCA 的 ATP 酶活性。然而,150μM 3BrPA 可使 Ca(2+)摄取活性显著抑制 80%。这些结果表明 3BrPA 具有将 ATP 水解与钙转运活性解耦的能力。此外,我们观察到在含有不同 3BrPA 浓度的反应介质中加入 2mM 还原型谷胱甘肽(GSH)可促进 ATP 酶活性增加 40%,并保护 3BrPA 对钙摄取活性的抑制作用。这种衍生化伴随着还原型半胱氨酸(Cys)的减少,表明 GSH 和 3BrPA 通过 GSH 介导的丙酮酸化和/或 S-谷胱甘肽化增加 SERCA 活性和转运,在 SERCA 的关键 Cys 残基上。