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克罗塔明细胞穿透纳米载体:癌症靶向及潜在的生物技术和/或医学应用

Crotamine Cell-Penetrating Nanocarriers: Cancer-Targeting and Potential Biotechnological and/or Medical Applications.

作者信息

Hayashi Mirian A F, Campeiro Joana Darc, Porta Lucas Carvalho, Szychowski Brian, Alves Wendel Andrade, Oliveira Eduardo B, Kerkis Irina, Daniel Marie-Christine, Karpel Richard L

机构信息

Departamento de Farmacologia, Universidade Federal de São Paulo (UNIFESP), São Paulo, Brazil.

Department of Chemistry and Biochemistry, University of Maryland Baltimore County, Baltimore, MD, USA.

出版信息

Methods Mol Biol. 2020;2118:61-89. doi: 10.1007/978-1-0716-0319-2_5.

Abstract

Crotamine is a basic, 42-residue polypeptide from snake venom that has been shown to possess cell-penetrating properties. Here we describe the preparation, purification, biochemical and biophysical analysis of venom-derived, recombinant, chemically synthesized, and fluorescent-labeled crotamine. We also describe the formation and characterization of crotamine-DNA and crotamine-RNA nanoparticles; and the delivery of these nanoparticles into cells and animals. Crotamine forms nanoparticles with a variety of DNA and RNA molecules, and crotamine-plasmid DNA nanoparticles are selectively delivered into actively proliferating cells in culture or in living organisms such as mice, Plasmodium, and worms. As such, these nanoparticles could form the basis for a nucleic acid drug-delivery system. We also describe here the design and characterization of crotamine-functionalized gold nanoparticles, and the delivery of these nanoparticles into cells. We also evaluated the viability of using the combination of crotamine with silica nanoparticles in animal models, aiming to provide slow delivery, and to decrease the crotamine doses needed for the biological effects. In addition, the efficacy of administering crotamine orally was also demonstrated.

摘要

巴曲酶是一种来自蛇毒的碱性42肽,已被证明具有细胞穿透特性。在此,我们描述了毒液衍生的、重组的、化学合成的和荧光标记的巴曲酶的制备、纯化、生化和生物物理分析。我们还描述了巴曲酶-DNA和巴曲酶-RNA纳米颗粒的形成和表征;以及这些纳米颗粒向细胞和动物的递送。巴曲酶与多种DNA和RNA分子形成纳米颗粒,巴曲酶-质粒DNA纳米颗粒被选择性地递送至培养物中或诸如小鼠、疟原虫和蠕虫等活生物体中的活跃增殖细胞。因此,这些纳米颗粒可构成核酸药物递送系统的基础。我们在此还描述了巴曲酶功能化金纳米颗粒的设计和表征,以及这些纳米颗粒向细胞的递送。我们还评估了在动物模型中使用巴曲酶与二氧化硅纳米颗粒组合的可行性,旨在实现缓慢递送,并减少产生生物学效应所需的巴曲酶剂量。此外,还证明了口服巴曲酶的有效性。

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