Wyss M, Wallimann T, Köhrle J
Swiss Federal Institute of Technology, Institute for Cell Biology, ETH-Hönggerberg, Zürich.
Biochem J. 1993 Apr 15;291 ( Pt 2)(Pt 2):463-72. doi: 10.1042/bj2910463.
Besides their well-known regulation of transcription by binding to nuclear receptors, thyroid hormones have been suggested to have direct effects on mitochondria. In a previous study, incubation of rat heart mitochondria with 125I-labelled N-bromoacetyl-3,3',5-tri-iodo-L-thyronine (BrAcT3), a thyroid hormone derivative with an alkylating side chain, resulted in the selective labelling of a protein doublet around M(r) 45,000 on SDS/polyacrylamide gels [Rasmussen, Köhrle, Rokos and Hesch (1989) FEBS Lett. 255, 385-390]. Now, this protein doublet has been identified as mitochondrial creatine kinase (Mi-CK). Immunoblotting experiments with the cytoplasmic and mitochondrial fractions of rat heart, brain and liver, as well as inactivation studies with the purified chicken CK isoenzymes have further demonstrated that all four CK isoenzymes (Mia-, Mib-, M- and B-CK) are indeed selectively labelled by BrAcT3. However, in contrast with their bromoalkyl derivatives, thyroid hormones themselves did not compete for CK labelling, suggesting that not the thyroid hormone moiety but rather the bromoacetyl-driven alkylation of the highly reactive 'essential' thiol group of CK accounts for this selective labelling. Therefore the assumption that CK isoenzymes are thyroid-hormone-binding proteins has to be dismissed. Instead, bromoacetyl-based reagents may allow a very specific covalent modification and inactivation of CK isoenzymes in vitro and in vivo.
除了通过与核受体结合对转录进行众所周知的调控外,甲状腺激素还被认为对线粒体有直接作用。在先前的一项研究中,用125I标记的N-溴乙酰基-3,3',5-三碘-L-甲状腺原氨酸(BrAcT3,一种带有烷基化侧链的甲状腺激素衍生物)孵育大鼠心脏线粒体,在SDS/聚丙烯酰胺凝胶上导致了Mr约45,000处一种蛋白质双峰的选择性标记[拉斯穆森、科尔勒、罗科斯和赫施(1989年)《欧洲生物化学学会联合会快报》255, 385 - 390]。现在,这种蛋白质双峰已被鉴定为线粒体肌酸激酶(Mi-CK)。用大鼠心脏、大脑和肝脏的细胞质和线粒体部分进行的免疫印迹实验,以及对纯化的鸡CK同工酶的失活研究进一步证明,所有四种CK同工酶(Mia-、Mib-、M-和B-CK)确实都被BrAcT3选择性标记。然而,与它们的溴烷基衍生物不同,甲状腺激素本身并不竞争CK标记,这表明不是甲状腺激素部分,而是溴乙酰驱动的CK高反应性“必需”巯基的烷基化导致了这种选择性标记。因此,CK同工酶是甲状腺激素结合蛋白的假设必须被摒弃。相反,基于溴乙酰的试剂可能允许在体外和体内对CK同工酶进行非常特异性的共价修饰和失活。