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通过离子选择性形成分子间 G-四链体和配体结合来直接检测血液钾离子

Direct Fluorescent Detection of Blood Potassium by Ion-Selective Formation of Intermolecular G-Quadruplex and Ligand Binding.

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Molecular Science and Biomedicine Laboratory, Hunan University , Changsha 410082, P. R. China.

School of Chemistry and Biological Engineering, Changsha University of Science and Technology , Changsha 410004, P. R. China.

出版信息

Anal Chem. 2016 Sep 20;88(18):9285-92. doi: 10.1021/acs.analchem.6b02667. Epub 2016 Sep 2.

Abstract

G-quadruplex analogues have been widely used as molecular tools for detection of potassium ion (K(+)). However, interference from a higher concentration of sodium ion (Na(+)), enzymatic degradation of the oligonucleotide, and background absorption and fluorescence of blood samples have all limited the use of G-quadruplex for direct detection of K(+) in blood samples. Here, we reported, for the first time, an intermolecular G-quadruplex-based assay capable of direct fluorescent detection of blood K(+). Increased stringency of intermolecular G-quadruplex formation based on our screened G-rich oligonucleotide (5'-TGAGGGA GGGG-3') provided the necessary selectivity for K(+) against Na(+) at physiological ion level. To increase long-term stability of oligonucleotide in blood, the screened oligonucleotide was modified with an inverted thymine nucleotide whose 3'-terminus was connected to the 3'-terminus of the upstream nucleotide, acting as a blocking group to greatly improve antinuclease stability. Lastly, to avoid interference from background absorption and autofluorescence of blood, a G-quadruplex-binding, two-photon-excited ligand, EBMVC-B, was synthesized and chosen as the fluorescence reporter. Thus, based on selective K(+) ion-induced formation of intermolecular G-quadruplex and EBMVC-B binding, this approach could linearly respond to K(+) from 0.5 to 10 mM, which matches quite well with the physiologically relevant concentration of blood K(+). Moreover, the system was highly selective for K(+) against other metal ions, including Na(+), Ca(2+), Mg(2+), Zn(2+) common in blood. The practical application was demonstrated by direct detection of K(+) from real blood samples by two-photon fluorescence technology. To the best of our knowledge, this is the first attempt to exploit molecular G-quadruplex-based fluorescent sensing for direct assay of blood target. As such, we expect that it will promote the design and practical application of similar DNA-based sensors in complex real systems.

摘要

G-四链体类似物已被广泛用作检测钾离子 (K(+)) 的分子工具。然而,由于钠离子 (Na(+)) 浓度较高、寡核苷酸的酶降解以及血液样本的背景吸收和荧光等因素的干扰,限制了 G-四链体在血液样本中直接检测 K(+) 的应用。在这里,我们首次报道了一种基于分子内 G-四链体的测定方法,能够直接荧光检测血液中的 K(+)。基于我们筛选出的富含 G 的寡核苷酸(5'-TGAGGGA GGGG-3'),增加分子内 G-四链体形成的严格性,为生理离子水平下 K(+) 对 Na(+) 的选择性提供了必要条件。为了提高寡核苷酸在血液中的长期稳定性,筛选出的寡核苷酸用倒置的胸腺嘧啶核苷酸修饰,其 3'-末端与上游核苷酸的 3'-末端相连,作为阻断基团,大大提高了抗核酸酶稳定性。最后,为了避免血液背景吸收和自发荧光的干扰,合成了一种 G-四链体结合的双光子激发配体 EBMVC-B,并将其用作荧光报告分子。因此,基于选择性 K(+) 离子诱导形成的分子内 G-四链体和 EBMVC-B 结合,该方法可以线性响应 0.5 至 10 mM 的 K(+),与血液中 K(+) 的生理相关浓度非常吻合。此外,该系统对 K(+) 具有高度选择性,可抵抗包括 Na(+)、Ca(2+)、Mg(2+)和 Zn(2+)在内的常见于血液中的其他金属离子。通过双光子荧光技术,直接从实际血液样本中检测 K(+),验证了该系统的实际应用。据我们所知,这是首次尝试利用基于分子 G-四链体的荧光传感直接测定血液靶标。因此,我们期望这将促进类似基于 DNA 的传感器在复杂实际系统中的设计和实际应用。

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