Institute of Chemical Biology and Nanomedicine, College of Chemistry and Chemical Engineering , Hunan University , Changsha , Hunan 410082 , China.
CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety and CAS Center for Excellence in Nanoscience , National Center for Nanoscience and Technology , Beijing 100190 , China.
J Am Chem Soc. 2018 Dec 19;140(50):17656-17665. doi: 10.1021/jacs.8b09867. Epub 2018 Dec 4.
Spatial and temporal distributions of metal ions in vitro and in vivo are crucial in our understanding of the roles of metal ions in biological systems, and yet there is a very limited number of methods to probe metal ions with high space and time resolution, especially in vivo. To overcome this limitation, we report a Zn-specific near-infrared (NIR) DNAzyme nanoprobe for real-time metal ion tracking with spatiotemporal control in early embryos and larvae of zebrafish. By conjugating photocaged DNAzymes onto lanthanide-doped upconversion nanoparticles (UCNPs), we have achieved upconversion of a deep tissue penetrating NIR 980 nm light into 365 nm emission. The UV photon then efficiently photodecages a substrate strand containing a nitrobenzyl group at the 2'-OH of adenosine ribonucleotide, allowing enzymatic cleavage by a complementary DNA strand containing a Zn-selective DNAzyme. The product containing a visible FAM fluorophore that is initially quenched by BHQ1 and Dabcyl quenchers is released after cleavage, resulting in higher fluorescent signals. The DNAzyme-UCNP probe enables Zn sensing by exciting in the NIR biological imaging window in both living cells and zebrafish embryos and detecting in the visible region. In this study, we introduce a platform that can be used to understand the Zn distribution with spatiotemporal control, thereby giving insights into the dynamical Zn ion distribution in intracellular and in vivo models.
金属离子在体外和体内的时空分布对于理解金属离子在生物系统中的作用至关重要,但目前能够以高时空分辨率探测金属离子的方法非常有限,特别是在体内。为了克服这一限制,我们报告了一种锌特异性近红外(NIR)DNA zyme 纳米探针,用于实时跟踪金属离子,并具有时空控制能力,可用于斑马鱼早期胚胎和幼虫。通过将光封闭 DNAzyme 缀合到镧系掺杂上转换纳米粒子(UCNPs)上,我们实现了将深部组织穿透的 NIR980nm 光上转换为 365nm 发射。然后,UV 光子有效地光解含有硝基苄基的碱基链,该碱基链位于腺苷核糖核苷酸的 2'-OH 上,允许互补的 DNA 链中含有锌选择性 DNAzyme 的酶切。该产物含有一个可见的 FAM 荧光团,最初被 BHQ1 和 Dabcyl 淬灭剂猝灭,在切割后被释放,从而产生更高的荧光信号。DNAzyme-UCNP 探针能够通过在活细胞和斑马鱼胚胎的近红外生物成像窗口中激发并在可见区域中检测来进行锌感应。在这项研究中,我们引入了一个平台,该平台可用于理解具有时空控制的锌分布,从而深入了解细胞内和体内模型中动态锌离子分布。
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