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抗菌肽和线粒体前序列影响线粒体偶联、呼吸作用及蛋白质导入。

Antibacterial peptides and mitochondrial presequences affect mitochondrial coupling, respiration and protein import.

作者信息

Hugosson M, Andreu D, Boman H G, Glaser E

机构信息

Department of Biochemistry, Arrhenius Laboratories for Natural Sciences, Stockholm University, Sweden.

出版信息

Eur J Biochem. 1994 Aug 1;223(3):1027-33. doi: 10.1111/j.1432-1033.1994.tb19081.x.

Abstract

Cecropins A and P1, antibacterial peptides from insects and from pig and some related peptides released respiratory control, inhibited protein import and at higher concentrations also inhibited respiration. However, PR-39, an antibacterial peptide from pig intestine, was found to be almost inert towards mitochondria. The concentrations at which the three mitochondrial functions were effected varied for different peptides. Melittin, magainin and Cecropin-A-(1,13)-Melittin(1,13)-NH2, a hybrid between cecropin A and melittin, were most potent, while the two cecropins acted at higher concentrations. The biosynthesis of cecropin A is known and the intermediates are synthesized. We have used four peptides from this pathway to investigate their effects on coupling, respiration and protein import into mitochondria. Mature cecropin A followed by the preproprotein were most aggressive whereas the intermediates were less active or inert. The efficiency of different derivatives of cecropin A as uncouplers correlates well with their capacity to release membrane potential measured as fluorescence quenching of Rhodamine 123. Inhibition of respiration was found to be dependent on membrane potential and was most pronounced with mature cecropin A, less so with its three precursors. We also found that three peptides derived from mitochondrial presequences showed antibacterial activity. It is concluded that, there are similarities in the functions of antibacterial peptides and mitochondrial presequences, uncoupling activity in mitochondria cannot be correlated with the antibacterial activity (contrary to a previous suggestion), the processing of preprocecropin A may have evolved in such a way that there is a minimum of membrane damage from the intermediates in the pathway, and peptides produced for delivery outside of an animal have evolved to be more aggressive against mitochondria than peptides for delivery inside of the animal.

摘要

天蚕素A和P1是来自昆虫、猪的抗菌肽,一些相关肽释放呼吸控制、抑制蛋白质导入,且在较高浓度时也抑制呼吸作用。然而,猪肠道抗菌肽PR-39被发现对线粒体几乎没有作用。三种线粒体功能受影响时的肽浓度因肽的不同而有所变化。蜂毒素、蛙皮素以及天蚕素A与蜂毒素的杂合体天蚕素A-(1,13)-蜂毒素(1,13)-NH2最为有效,而两种天蚕素在较高浓度时才起作用。天蚕素A的生物合成途径已知且中间产物已被合成。我们使用了该途径中的四种肽来研究它们对线粒体偶联、呼吸作用以及蛋白质导入的影响。成熟天蚕素A及其前原蛋白最具活性,而中间产物活性较低或无活性。天蚕素A不同衍生物作为解偶联剂的效率与其通过罗丹明123荧光猝灭测量的释放膜电位的能力密切相关。呼吸作用的抑制被发现依赖于膜电位,成熟天蚕素A最为显著,其三种前体则较弱。我们还发现源自线粒体前导序列的三种肽具有抗菌活性。结论是,抗菌肽和线粒体前导序列的功能存在相似性,线粒体中的解偶联活性与抗菌活性无关(与先前的观点相反),前原天蚕素A的加工过程可能以这样一种方式进化,即该途径中的中间产物对膜的损伤最小,并且为在动物体外传递而产生的肽进化得比对在动物体内传递的肽对线粒体更具攻击性。

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