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一种显著改进的多功能 Au-DNA 纳米粒子缀合物的制备方法,该缀合物经过光学和磁共振成像探针的修饰。

A Markedly Improved Synthetic Approach for the Preparation of Multifunctional Au-DNA Nanoparticle Conjugates Modified with Optical and MR Imaging Probes.

机构信息

Department of Chemistry, Molecular Biosciences, Neurobiology, Biomedical Engineering, and Radiology , Northwestern University , 2145 Sheridan Road , Evanston , Illinois 60208-3113 , United States.

出版信息

Bioconjug Chem. 2018 Nov 21;29(11):3544-3549. doi: 10.1021/acs.bioconjchem.8b00504. Epub 2018 Oct 10.

DOI:10.1021/acs.bioconjchem.8b00504
PMID:30193061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6268127/
Abstract

We describe a new, and vastly superior approach for labeling spherical nucleic acid conjugates (SNAs) with diagnostic probes. SNAs have been shown to provide the unique ability to traverse the cell membrane and deliver surface conjugated DNA into cells while preserving the DNA from nuclease degradation. Our previous work on preparing diagnostically labeled SNAs was labor intensive, relatively low yielding, and costly. Here, we describe a straightforward and facile preparation for labeling SNAs with optical and MR imaging probes with significantly improved physical properties. The synthesis of Gd(III) labeled DNA Au nanoparticle conjugates is achieved by sequential conjugation of 3'-thiol-modified oligonucleotides and cofunctionalization of the particle surface with the subsequent addition of 1,2 diothiolate modified chelates of Gd(III) (abbreviated: DNA-Gd@AuNP). This new generation of SNA conjugates has a 2-fold increase of DNA labeling and a 1.4-fold increase in Gd(III) loading compared to published constructs. Furthermore, the relaxivity ( r) is observed to increase 4.5-fold compared to the molecular dithiolane-Gd(III) complex, and 1.4-fold increase relative to previous particle constructs where the Gd(III) complexes were conjugated to the oligonucleotides rather than directly to the Au particle. Importantly, this simplified approach (2 steps) exploits the advantages of previous Gd(III) labeled SNA platforms; however, this new approach is scalable and eliminates modification of DNA for attaching the contrast agent, and the particles exhibit improved cell labeling.

摘要

我们描述了一种新的、优越的方法,用于用诊断探针标记球形核酸缀合物(SNA)。已经证明,SNA 具有独特的能力,可以穿透细胞膜,并将表面连接的 DNA 递送到细胞内,同时保护 DNA 免受核酸酶的降解。我们之前在制备诊断标记的 SNA 方面的工作劳动强度大、产量相对较低且成本高。在这里,我们描述了一种简单易行的方法,用于用光学和磁共振成像探针标记 SNA,这些探针具有显著改善的物理性质。通过顺序缀合 3'-巯基修饰的寡核苷酸和共功能化颗粒表面,随后添加 Gd(III)(简称:DNA-Gd@AuNP)的 1,2 二硫代酸盐修饰螯合物,实现了 Gd(III)标记的 DNA Au 纳米颗粒缀合物的合成。与已发表的构建体相比,这种新一代 SNA 缀合物的 DNA 标记增加了 2 倍,Gd(III)负载增加了 1.4 倍。此外,与分子二硫醇-Gd(III)配合物相比,弛豫率(r)观察到增加了 4.5 倍,与之前的颗粒构建体相比,增加了 1.4 倍,其中 Gd(III)配合物连接到寡核苷酸上,而不是直接连接到 Au 颗粒上。重要的是,这种简化的方法(2 步)利用了以前的 Gd(III)标记 SNA 平台的优势;然而,这种新方法是可扩展的,并消除了修饰 DNA 以连接造影剂的需要,并且颗粒表现出更好的细胞标记。