Atlante A, Passarella S, Quagliariello E, Moreno G, Salet C
Dipartimento di Biochimica e Biologia Molecolare, Università di Bari, Italy.
J Photochem Photobiol B. 1989 Oct;4(1):35-46. doi: 10.1016/1011-1344(89)80100-9.
To gain further insight into the mechanism by which irradiation of mitochondria in the presence of haematoporphyrin derivative (Photofrin II) (PF II) causes impairment of mitochondrial oxidative phosphorylation, the rate of ADP/ATP exchange via the ADP/ATP translocator was measured fluorometrically is isolated rat liver mitochondria. In accord with noncompetitive inhibition, PF II photosensitization decreases the maximum rate of exchange Vmax (20.8 and 9.6 nmol ATP effluxed min-1 x mg protein in the control and after 2 min irradiation, respectively) without changing the ADP affinity for the carrier (Km = 5 microM in both cases). Comparison of the rate of oxygen uptake by mitochondria stimulated by either ADP or by the uncoupler carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP) confirms that the adenine nucleotide carrier is a major target of photodynamic action which causes oxidative phosphorylation impairment.
为了进一步深入了解在血卟啉衍生物(卟吩姆钠II)(PF II)存在的情况下照射线粒体导致线粒体氧化磷酸化受损的机制,通过荧光法测定了分离的大鼠肝线粒体中经由ADP/ATP转位酶的ADP/ATP交换速率。与非竞争性抑制一致,PF II光致敏作用降低了最大交换速率Vmax(对照组和照射2分钟后分别为20.8和9.6 nmol ATP每分钟流出量x毫克蛋白质),而不改变ADP对载体的亲和力(两种情况下Km均为5 microM)。比较由ADP或解偶联剂羰基氰4-(三氟甲氧基)苯腙(FCCP)刺激的线粒体的氧摄取速率证实,腺嘌呤核苷酸载体是导致氧化磷酸化受损的光动力作用的主要靶点。