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荧光蛋白与 DNA 寡核苷酸的缀合。

Conjugation of fluorescent proteins with DNA oligonucleotides.

机构信息

Technische Universitat Dortmund, Fakultat Chemie, Biologisch-Chemische Mikrostrukturtechnik, Otto-Hahn Str. 6, D-44227 Dortmund, Germany.

出版信息

Bioconjug Chem. 2010 May 19;21(5):921-7. doi: 10.1021/bc900471q.

Abstract

This work describes the synthesis of covalent ssDNA conjugates of six fluorescent proteins, ECFP, EGFP, E(2)GFP, mDsRed, Dronpa, and mCherry, which were cloned with an accessible C-terminal cystein residue to enable site-selective coupling using a heterobispecific cross-linker. The resulting conjugates revealed similar fluorescence emission intensity to the unconjugated proteins, and the functionality of the tethered oligonucleotide was proven by specific Watson-Crick base pairing to cDNA-modified gold nanoparticles. Fluorescence spectroscopy analysis indicated that the fluorescence of the FP is quenched by the gold particle, and the extent of quenching varied with the intrinsic spectroscopic properties of FP as well as with the configuration of surface attachment. Since this study demonstrates that biological fluorophores can be selectively incorporated into and optically coupled with nanoparticle-based devices, applications in DNA-based nanofabrication can be foreseen.

摘要

这项工作描述了六种荧光蛋白(ECFP、EGFP、E(2)GFP、mDsRed、Dronpa 和 mCherry)的共价 ssDNA 缀合物的合成,这些荧光蛋白通过可及的 C 末端半胱氨酸残基克隆,以便使用杂双特异性交联剂进行选择性偶联。所得缀合物显示出与未缀合蛋白相似的荧光发射强度,并且通过与 cDNA 修饰的金纳米粒子的特异性 Watson-Crick 碱基配对证明了连接的寡核苷酸的功能。荧光光谱分析表明,金颗粒猝灭 FP 的荧光,猝灭程度随 FP 的固有光谱特性以及表面附着的构型而变化。由于这项研究表明生物荧光团可以选择性地掺入并与基于纳米粒子的器件光学偶联,因此可以预见其在基于 DNA 的纳米制造中的应用。

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