A Cell-penetrating Helical Polymer For siRNA Delivery to Mammalian Cells

被引:54
|
作者
Gabrielson, Nathan P. [2 ]
Lu, Hua [3 ]
Yin, Lichen [1 ]
Kim, Kyung Hoon [1 ]
Cheng, Jianjun [1 ]
机构
[1] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[2] Univ Illinois, Inst Genom Biol, Urbana, IL 61801 USA
[3] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
关键词
INTERFERING RNA SIRNA; IN-VIVO DELIVERY; GENE DELIVERY; HELA-CELLS; PEPTIDE; THERAPY; KNOCKING; HUMANS; DESIGN; POTENT;
D O I
10.1038/mt.2012.78
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cell-penetrating peptides (CPPs) are routinely used for intracellular delivery of a variety of cargo, including drugs, genes, and short interfering RNA (siRNA). Most CPPs are active only upon exposure to acidic environments inside of late endosomes, thereby facilitating the endosomal escape of internalized vectors. Here, we describe the generation of a synthetic polypeptide-PVBLG(n)-8-that is able to adopt a helical structure independent of pH. Like other CPPs, the helical structure of PVBLG(n)-8 allows the polypeptide to destabilize membranes. However, since the helix is stable at all physiologically relevant pH values between pH 2 and pH 7.4, the membrane permeation properties of PVBLG(n)-8 are irreversible. Given its pH-insensitive activity, our results suggest that PVBLG(n)-8 is able to facilitate efficient siRNA delivery by causing pore formation in the cell membranes through which either free or complexed siRNA is able to diffuse. This nonspecific form of entry into the cell cytosol may prove useful when trying to deliver siRNA to cells which have proven to be difficult to transfect.
引用
收藏
页码:1599 / 1609
页数:11
相关论文
共 50 条
  • [1] A New Potent Secondary Amphipathic Cell-penetrating Peptide for siRNA Delivery Into Mammalian Cells
    Crombez, Laurence
    Aldrian-Herrada, Gudrun
    Konate, Karidia
    Nguyen, Quan N.
    McMaster, Gary K.
    Brasseur, Robert
    Heitz, Frederic
    Divita, Gilles
    MOLECULAR THERAPY, 2009, 17 (01) : 95 - 103
  • [2] Cell-penetrating peptides for siRNA delivery to glioblastomas
    Srimanee, Artita
    Arvanitidou, Maria
    Kim, Kumjee
    Hallbrink, Mattias
    Langel, Ulo
    PEPTIDES, 2018, 104 : 62 - 69
  • [3] Versatility of cell-penetrating peptides for intracellular delivery of siRNA
    Singh, Tejinder
    Murthy, Akula S. N.
    Yang, Hye-Jin
    Im, Jungkyun
    DRUG DELIVERY, 2018, 25 (01) : 1996 - 2006
  • [4] Systemic siRNA delivery to tumors by cell-penetrating α-helical polypeptide-based metastable nanoparticles
    Liu, Yang
    Song, Ziyuan
    Zheng, Nan
    Nagasaka, Kenya
    Yin, Lichen
    Cheng, Jianjun
    NANOSCALE, 2018, 10 (32) : 15339 - 15349
  • [5] Cationic cell-penetrating peptides as vehicles for siRNA delivery
    Beloor, Jagadish
    Zeller, Skye
    Choi, Chang Seon
    Lee, Sang-Kyung
    Kumar, Priti
    THERAPEUTIC DELIVERY, 2015, 6 (04) : 491 - 507
  • [6] siRNA delivery using amphipathic cell-penetrating peptides into human hepatoma cells
    Furukawa, Kaori
    Tanaka, Masakazu
    Oba, Makoto
    BIOORGANIC & MEDICINAL CHEMISTRY, 2020, 28 (08)
  • [7] siRNA Delivery: From Lipids to Cell-penetrating Peptides and Their Mimics
    Gooding, Matt
    Browne, Lorcan P.
    Quinteiro, Filipa M.
    Selwood, David L.
    CHEMICAL BIOLOGY & DRUG DESIGN, 2012, 80 (06) : 787 - 809
  • [8] Perspectives and Challenges of Cell-Penetrating Peptides in Effective siRNA Delivery
    Yu, Zhiqiang
    Yu, Bin
    Kaye, Justin Boy
    Tang, Chenhong
    Chen, Shengxi
    Dong, Chenbo
    Shen, Bing
    NANO LIFE, 2014, 4 (04)
  • [9] A retro-inverso cell-penetrating peptide for siRNA delivery
    Anaïs Vaissière
    Gudrun Aldrian
    Karidia Konate
    Mattias F. Lindberg
    Carole Jourdan
    Anthony Telmar
    Quentin Seisel
    Frédéric Fernandez
    Véronique Viguier
    Coralie Genevois
    Franck Couillaud
    Prisca Boisguerin
    Sébastien Deshayes
    Journal of Nanobiotechnology, 15
  • [10] Cell-penetrating peptide TAT modified chitosan for siRNA delivery
    Yang, Feifei
    Li, Yunfei
    Huang, Wei
    Chen, Wei
    Jin, Mingji
    Gao, Zhonggao
    JOURNAL OF CONTROLLED RELEASE, 2013, 172 (01) : E100 - E101