细菌锌-金属磷脂酶C

R. Titball, A. Basak
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引用次数: 7

摘要

细菌锌金属磷脂酶C仅由革兰氏阳性细菌产生,其特征是在活性位点存在多达三个锌离子。一些锌-金属磷脂酶C,如产气荚膜梭菌的α -毒素,是强效毒素,在疾病的发病机制中起关键作用。毒性似乎与酶与宿主细胞膜磷脂相互作用的能力以及磷脂酰胆碱和鞘磷脂的水解有关。锌-金属磷脂酶的作用方式的重要见解已经从这组成员的晶体结构的知识中获得。所有的酶都具有酶结构域,但只有一些锌-金属磷脂酶具有在膜磷脂识别中起关键作用的结构域。这个结构域的存在似乎对毒性是必要的,但并非所有拥有这个结构域的酶都是有毒的。一些研究表明,膜活性毒素,如产气荚膜梭菌α毒素,可能被用于治疗癌性疾病。
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The Bacterial Zinc‐Metallophospholipases C
The bacterial zinc‐metallophospholipases C are produced only by gram‐positive bacteria and are characterised on the basis of the presence of up to three zinc ions in the active site. Some zinc‐metallophospholipases C, like the α‐toxin of Clostridium perfringens, are potent toxins and play key roles in the pathogenesis of disease. Toxicity appears to be related to the ability of the enzyme to interact with phospholipids in host cell membranes and to the hydrolysis of both phosphatidylcholine and sphingomyelin. Significant insight into the mode of action of the zinc‐metallophospholipases has been gained from knowledge of the crystal structures of several members of this group. All of the enzymes possess an enzymatic domain, but only some zinc‐metallophospholipases possess a domain that can play a key role in the recognition of membrane phospholipids. The presence of this domain appears to be necessary for toxicity, but not all enzymes that possess this domain are toxic. Several studies have indicated that membrane active toxins, such as C. perfringens α‐toxin, might be exploited for the treatment of oncogenic disease.
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