• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1093/nar/22.24.5439
PMID:7816636
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC332094/
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/bc37/332094/53228bff277f/nar00048-0306-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc37/332094/a9ad6dc337b9/nar00048-0305-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc37/332094/fa2ae997eac2/nar00048-0305-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc37/332094/53228bff277f/nar00048-0306-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc37/332094/a9ad6dc337b9/nar00048-0305-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc37/332094/fa2ae997eac2/nar00048-0305-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc37/332094/53228bff277f/nar00048-0306-a.jpg

相似文献

1
Enhanced resistance to nuclease degradation of nucleic acids complexed to asialoglycoprotein-polylysine carriers.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。
Nucleic Acids Res. 1994 Dec 11;22(24):5439-46. doi: 10.1093/nar/22.24.5439.
2
Preparation of asialoorosomucoid-polylysine conjugates.去唾液酸血清类黏蛋白-聚赖氨酸缀合物的制备
Bioconjug Chem. 1994 Jul-Aug;5(4):306-11. doi: 10.1021/bc00028a004.
3
Targeted delivery of DNA using YEE(GalNAcAH)3, a synthetic glycopeptide ligand for the asialoglycoprotein receptor.使用YEE(GalNAcAH)3进行DNA的靶向递送,YEE(GalNAcAH)3是一种用于去唾液酸糖蛋白受体的合成糖肽配体。
Bioconjug Chem. 1994 Nov-Dec;5(6):612-20. doi: 10.1021/bc00030a017.
4
Receptor-mediated gene delivery and expression in vivo.体内受体介导的基因递送与表达
J Biol Chem. 1988 Oct 15;263(29):14621-4.
5
Modulation of the molecular conformation of a hepatocyte-targeting gene drug in order to improve its expression efficiency in vitro.调节一种靶向肝细胞的基因药物的分子构象,以提高其体外表达效率。
Chin J Dig Dis. 2005;6(1):37-42. doi: 10.1111/j.1443-9573.2005.00186.x.
6
Targeted delivery of DNA encoding herpes simplex virus type-1 glycoprotein D enhances the cellular response to primary viral challenge.靶向递送编码单纯疱疹病毒1型糖蛋白D的DNA可增强细胞对原发性病毒攻击的反应。
Arch Dermatol Res. 2000 Nov;292(11):542-9. doi: 10.1007/s004030000181.
7
A novel immunization method to induce cytotoxic T-lymphocyte responses (CTL) against plasmid-encoded herpes simplex virus type-1 glycoprotein D.一种诱导细胞毒性T淋巴细胞应答(CTL)以对抗质粒编码的单纯疱疹病毒1型糖蛋白D的新型免疫方法。
Vaccine. 1999 Mar 5;17(9-10):1091-9. doi: 10.1016/s0264-410x(98)00326-0.
8
DNA toroids: stages in condensation.DNA超螺旋环:凝聚阶段
Biochemistry. 1999 Oct 19;38(42):14069-76. doi: 10.1021/bi990901o.
9
Improvement of receptor-mediated gene delivery to HepG2 cells using an amphiphilic gelling agent.使用两亲性凝胶剂改善受体介导的基因向HepG2细胞的递送
Biotechnol Appl Biochem. 2000 Aug;32(1):21-6. doi: 10.1042/ba20000022.
10
Receptor-mediated in vitro gene transformation by a soluble DNA carrier system.可溶性DNA载体系统介导的体外受体基因转化
J Biol Chem. 1987 Apr 5;262(10):4429-32.

引用本文的文献

1
Advanced biopolymeric materials and nanosystems for RNA/DNA vaccines: a review.高级生物聚合材料和纳米系统用于 RNA/DNA 疫苗:综述。
Nanomedicine (Lond). 2024;19(24):2027-2043. doi: 10.1080/17435889.2024.2382077. Epub 2024 Aug 7.
2
Synthesis, Biophysical Properties, and Antitumor Activity of Antisense Oligonucleotides Conjugated with Anisamide.与茴香酰胺偶联的反义寡核苷酸的合成、生物物理性质及抗肿瘤活性
Pharmaceutics. 2023 Jun 2;15(6):1645. doi: 10.3390/pharmaceutics15061645.
3
Non-Viral Carriers for Nucleic Acids Delivery: Fundamentals and Current Applications.

本文引用的文献

1
Fate of DNA targeted to the liver by asialoglycoprotein receptor-mediated endocytosis in vivo. Prolonged persistence in cytoplasmic vesicles after partial hepatectomy.去唾液酸糖蛋白受体介导的内吞作用靶向肝脏的DNA在体内的命运。部分肝切除术后在细胞质囊泡中持续存在较长时间。
J Biol Chem. 1993 May 25;268(15):11265-71.
2
Hepatic gene therapy: adenovirus enhancement of receptor-mediated gene delivery and expression in primary hepatocytes.肝脏基因治疗:腺病毒增强受体介导的基因递送及在原代肝细胞中的表达
Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2122-6. doi: 10.1073/pnas.90.6.2122.
3
Incorporation of adenovirus into a ligand-based DNA carrier system results in retention of original receptor specificity and enhances targeted gene expression.
用于核酸递送的非病毒载体:基础与当前应用
Life (Basel). 2023 Mar 29;13(4):903. doi: 10.3390/life13040903.
4
Gene Therapy: The Next-Generation Therapeutics and Their Delivery Approaches for Neurological Disorders.基因治疗:用于神经系统疾病的下一代治疗方法及其递送途径。
Front Genome Ed. 2022 Jun 22;4:899209. doi: 10.3389/fgeed.2022.899209. eCollection 2022.
5
Nanotechnology-Based Strategies to Overcome Current Barriers in Gene Delivery.基于纳米技术的策略来克服基因传递中的当前障碍。
Int J Mol Sci. 2021 Aug 9;22(16):8537. doi: 10.3390/ijms22168537.
6
Cytocompatibility of stabilized black phosphorus nanosheets tailored by directly conjugated polymeric micelles for human breast cancer therapy.通过直接共轭聚合物胶束稳定化的黑磷纳米片用于人乳腺癌治疗的细胞相容性。
Sci Rep. 2021 Apr 29;11(1):9304. doi: 10.1038/s41598-021-88791-7.
7
Modulating the Crosstalk between the Tumor and the Microenvironment Using SiRNA: A Flexible Strategy for Breast Cancer Treatment.使用小干扰RNA调节肿瘤与微环境之间的串扰:一种用于乳腺癌治疗的灵活策略
Cancers (Basel). 2020 Dec 13;12(12):3744. doi: 10.3390/cancers12123744.
8
DNA Methylation Profiles and Their Diagnostic Utility in BC.BC 中的 DNA 甲基化图谱及其诊断效用。
Dis Markers. 2019 May 6;2019:6328503. doi: 10.1155/2019/6328503. eCollection 2019.
9
Correlating blood-based DNA methylation markers and prostate cancer risk in African-American men.关联基于血液的 DNA 甲基化标志物与非裔美国男性前列腺癌风险。
PLoS One. 2018 Sep 11;13(9):e0203322. doi: 10.1371/journal.pone.0203322. eCollection 2018.
10
It's All in the Delivery: Designing Hydrogels for Cell and Non-viral Gene Therapies.一切都在传递中:设计水凝胶用于细胞和非病毒基因治疗。
Mol Ther. 2018 Sep 5;26(9):2087-2106. doi: 10.1016/j.ymthe.2018.07.022. Epub 2018 Aug 4.
将腺病毒整合到基于配体的DNA载体系统中,可保留原始受体特异性并增强靶向基因表达。
J Biol Chem. 1994 Apr 15;269(15):11542-6.
4
Preparation of asialoorosomucoid-polylysine conjugates.去唾液酸血清类黏蛋白-聚赖氨酸缀合物的制备
Bioconjug Chem. 1994 Jul-Aug;5(4):306-11. doi: 10.1021/bc00028a004.
5
Partial characterization of the sialic acid-free forms of alpha-1-acid glycoprotein from human plasma.人血浆中无唾液酸形式的α-1-酸性糖蛋白的部分特性分析
Biochem J. 1967 Aug;104(2):361-8. doi: 10.1042/bj1040361.
6
High resolution acrylamide gel electrophoresis of histones.组蛋白的高分辨率丙烯酰胺凝胶电泳
Arch Biochem Biophys. 1969 Mar;130(1):337-46. doi: 10.1016/0003-9861(69)90042-3.
7
A simple technique for the isolation of orosomucoid from normal and pathological sera.从正常和病理血清中分离类粘蛋白的一种简单技术。
Biochim Biophys Acta. 1966 Jul 27;124(1):209-11. doi: 10.1016/0304-4165(66)90336-9.
8
Oligodeoxynucleotide stability in subcellular extracts and culture media.亚细胞提取物和培养基中寡脱氧核苷酸的稳定性
J Biochem Biophys Methods. 1986 Sep;13(2):97-102. doi: 10.1016/0165-022x(86)90021-7.
9
Receptor-mediated in vitro gene transformation by a soluble DNA carrier system.可溶性DNA载体系统介导的体外受体基因转化
J Biol Chem. 1987 Apr 5;262(10):4429-32.
10
Receptor-mediated gene delivery and expression in vivo.体内受体介导的基因递送与表达
J Biol Chem. 1988 Oct 15;263(29):14621-4.