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使用肽偶联肽核酸(PNA)在链球菌中验证用于反义治疗的合适载体分子和靶基因

Validation of Suitable Carrier Molecules and Target Genes for Antisense Therapy Using Peptide-Coupled Peptide Nucleic Acids (PNAs) in Streptococci.

作者信息

Barkowsky Gina, Kreikemeyer Bernd, Patenge Nadja

机构信息

Institute of Medical Microbiology, Virology and Hygiene, University Medicine Rostock, Rostock, Germany.

出版信息

Methods Mol Biol. 2020;2136:339-345. doi: 10.1007/978-1-0716-0467-0_27.

Abstract

Antisense peptide nucleic acids (PNAs) targeting genes involved in metabolism or virulence are a possible means to treat infections or to investigate pathogenic bacteria. Potential targets include essential genes, virulence factor genes, or antibiotic resistance genes. For efficient cellular uptake, PNAs can be coupled to cell-penetrating peptides (CPPs). CPPs are peptides that serve as molecular transporters and are characterized by a comparably low cytotoxicity. So far, there is only limited information about CPPs that mediate PNA uptake by Gram-positive bacteria. Here, we describe two methods to identify suitable CPP-antisense PNA conjugates, novel carrier molecules, and efficient target genes for streptococcal species and to evaluate their antimicrobial efficiency.

摘要

靶向参与代谢或毒力相关基因的反义肽核酸(PNA)是治疗感染或研究病原菌的一种可能手段。潜在靶点包括必需基因、毒力因子基因或抗生素抗性基因。为了实现有效的细胞摄取,PNA可与细胞穿透肽(CPP)偶联。CPP是作为分子转运体的肽,其特征是细胞毒性相对较低。到目前为止,关于介导革兰氏阳性菌摄取PNA的CPP的信息还很有限。在此,我们描述了两种方法,用于鉴定适合链球菌属的CPP-反义PNA偶联物、新型载体分子和有效靶基因,并评估它们的抗菌效率。

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