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与去唾液酸糖蛋白-聚赖氨酸载体复合的核酸对核酸酶降解的抗性增强。

Enhanced resistance to nuclease degradation of nucleic acids complexed to asialoglycoprotein-polylysine carriers.

作者信息

Chiou H C, Tangco M V, Levine S M, Robertson D, Kormis K, Wu C H, Wu G Y

机构信息

Gene Therapy Group, TargeTech Inc., Carlsbad, CA 92008.

出版信息

Nucleic Acids Res. 1994 Dec 11;22(24):5439-46. doi: 10.1093/nar/22.24.5439.

Abstract

We have previously shown targeting of DNA to hepatocytes using an asialoorosomucoid-polylysine (AsOR-PL) carrier system. The AsOR-PL conjugate condenses DNA and facilitates entry via specific receptor-ligand interactions. In these studies, our objective was to determine if AsOR-PL conjugates protect bound DNA from nuclease attack. Double-stranded plasmid or single-stranded oligonucleotide DNA, alone or bound to conjugate, was incubated under conditions mimicking those encountered during in vitro and in vivo transfections. The results showed that complexed DNA was effectively protected from degradation by serum nucleases. Degradation of single-stranded oligonucleotides was inhibited 3- to 6-fold in serum during 5 hours of incubation. For complexed plasmids, greater than 90% remained full-length during 1.5 and 3 hour incubations in serum or culture medium containing 10% serum, respectively. Uncomplexed plasmid was completely degraded after 15 minutes in serum or 60 minutes in medium. In cell lysates, the conjugate was not effective in inhibiting endonuclease activity; plasmids were readily converted from supercoiled to open circular and linear forms. However, the resultant nicked forms were substantially protected from further degradation during one hour of incubation compared to plasmid alone. Under all conditions complexed DNA did not readily dissociate from the conjugate. Overall, for both single and double-stranded DNA, AsOR-PL conjugates conferred substantial protection from nuclease degradation.

摘要

我们之前已经证明,使用去唾液酸糖蛋白-聚赖氨酸(AsOR-PL)载体系统可将DNA靶向递送至肝细胞。AsOR-PL偶联物可使DNA凝聚,并通过特定的受体-配体相互作用促进其进入细胞。在这些研究中,我们的目的是确定AsOR-PL偶联物是否能保护结合的DNA免受核酸酶攻击。双链质粒或单链寡核苷酸DNA,单独或与偶联物结合后,在模拟体外和体内转染过程中所遇到的条件下进行孵育。结果表明,复合DNA能有效免受血清核酸酶的降解。在5小时的孵育过程中,血清中单链寡核苷酸的降解受到3至6倍的抑制。对于复合质粒,在含有10%血清的血清或培养基中分别孵育1.5小时和3小时后,超过90%的质粒仍保持全长。未复合的质粒在血清中15分钟或培养基中60分钟后完全降解。在细胞裂解物中,偶联物在抑制核酸内切酶活性方面无效;质粒很容易从超螺旋形式转变为开环和线性形式。然而,与单独的质粒相比,在孵育1小时期间,产生的切口形式能得到显著保护,免受进一步降解。在所有条件下,复合DNA都不易与偶联物解离。总体而言,对于单链和双链DNA,AsOR-PL偶联物都能提供显著的保护,使其免受核酸酶降解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc37/332094/a9ad6dc337b9/nar00048-0305-a.jpg

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