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肽核酸依赖性基因化学:肽和寡核苷酸与质粒DNA的稳定偶联

PNA-dependent gene chemistry: stable coupling of peptides and oligonucleotides to plasmid DNA.

作者信息

Zelphati O, Liang X, Nguyen C, Barlow S, Sheng S, Shao Z, Felgner P L

机构信息

Gene Therapy Systems, San Diego, CA, USA.

出版信息

Biotechniques. 2000 Feb;28(2):304-10, 312-4, 316. doi: 10.2144/00282rr01.

Abstract

Two approaches are described for stably conjugating peptides, proteins and oligonucleotides onto plasmid DNA. Both methods use a peptide nucleic acid (PNA) clamp, which binds irreversibly and specifically to a binding site cloned into the plasmid. The first approach uses a biotin-conjugated PNA clamp that can be used to introduce functional biotin groups onto the plasmid to which streptavidin can bind. Atomic force microscopy images of linearized plasmid show streptavidin localized at the predicted PNA binding site on the DNA strand. Peptides and oligonucleotides containing free thiol groups were conjugated to maleimide streptavidin, and these streptavidin conjugates were bound to the biotin-PNA-labeled plasmid. In this way, peptides and oligonucleotides could be brought into stable association with the plasmid. A second approach used a maleimide-conjugated PNA clamp. Methods are described for conjugating thiolated peptides and oligonucleotides directly to the maleimide-PNA-DNA hybrid. This straightforward technology offers an easy approach to introduce functional groups onto plasmid DNA without disturbing its transcriptional activity.

摘要

本文描述了两种将肽、蛋白质和寡核苷酸稳定偶联到质粒DNA上的方法。两种方法均使用肽核酸(PNA)钳,该钳可不可逆且特异性地结合克隆到质粒中的结合位点。第一种方法使用生物素偶联的PNA钳,可用于将功能性生物素基团引入质粒,链霉亲和素可与之结合。线性化质粒的原子力显微镜图像显示链霉亲和素定位于DNA链上预测的PNA结合位点。含有游离巯基的肽和寡核苷酸与马来酰亚胺链霉亲和素偶联,这些链霉亲和素偶联物与生物素-PNA标记的质粒结合。通过这种方式,肽和寡核苷酸可以与质粒形成稳定的结合。第二种方法使用马来酰亚胺偶联的PNA钳。文中描述了将硫醇化肽和寡核苷酸直接偶联到马来酰亚胺-PNA-DNA杂交体上的方法。这种简单的技术提供了一种在不干扰质粒转录活性的情况下将官能团引入质粒DNA的简便方法。

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