We have previously described a novel cancer chemotherapeutic approach based on the induction of apoptosis in targeted cells by homing pro-apoptotic peptides. In order to improve this approach we developed a computational method (approach for detecting potential apoptotic peptides, APAP) to detect short PAPs, based on the prediction of the helical content of peptides, the hydrophobic moment, and the isoelectric point. PAPs are toxic against bacteria and mitochondria, but not against mammalian cells when applied extracellularly. Among other peptides, substance P was identified as a PAP and subsequently demonstrated to be a pro-apoptotic peptide experimentally. APAP thus provides a method to detect and ultimately improve pro-apoptotic peptides for chemotherapy.

译文

我们先前已经描述了一种新的癌症化学治疗方法,该方法基于通过归巢促凋亡肽诱导靶向细胞凋亡。为了改进这种方法,我们基于对肽的螺旋含量,疏水矩和等电点的预测,开发了一种计算方法 (用于检测潜在凋亡肽的方法,APAP) 来检测短PAPs。PAPs对细菌和线粒体具有毒性,但在细胞外使用时对哺乳动物细胞没有毒性。在其他肽中,p物质被鉴定为PAP,随后通过实验证明是促凋亡肽。因此,APAP提供了一种检测并最终改善用于化学疗法的促凋亡肽的方法。

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