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Basic peptide-morpholino oligomer conjugate that is very effective in killing bacteria by gene-specific and nonspecific modes

机译:基本的肽-吗啉代寡聚物结合物,通过基因特异性和非特异性方式对杀死细菌非常有效

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摘要

Basic peptides covalently linked to nucleic acids, or chemically modified nucleic acids, enable the insertion of such a conjugate into bacteria grown in liquid medium and mammalian cells in tissue culture. A unique peptide, derived from human T cells, has been employed in a chemical synthesis to make a conjugate with a morpholino oligonucleotide. This new conjugate is at least 10- to 100-fold more effective than previous peptides used in altering the phenotype of host bacteria if the external guide sequence methodology is employed in these experiments. Bacteria with target genes expressing chloramphenicol resistance, penicillin resistance, or gyrase A function can effectively be reduced in their expression and the host cells killed. Several bacteria are susceptible to this treatment, which has a broad range of potency. The loss in viability of bacteria is not due only to complementarity with a target RNA and the action of RNase P, but also to a non-gene-specific tight binding of the complexed nontargeted RNA to the basic polypeptide-morpholino oligonucleotide.
机译:与核酸或化学修饰的核酸共价连接的碱性肽能够将这种缀合物插入在液体培养基中生长的细菌和组织培养物中的哺乳动物细胞中。源自人T细胞的独特肽已用于化学合成中,以与吗啉代寡核苷酸形成偶联物。如果在这些实验中采用外部指导序列方法,那么这种新的偶联物比用于改变宿主细菌表型的以前的肽至少有效10至100倍。具有表达氯霉素抗性,青霉素抗性或回旋酶A功能的靶基因的细菌可有效降低其表达并杀死宿主细胞。几种细菌对这种治疗敏感,具有广泛的效力。细菌生存力的丧失不仅是由于与靶RNA的互补性和RNase P的作用,还归因于复合的非靶RNA与基本多肽-吗啉代寡核苷酸的非基因特异性紧密结合。

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