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双叠氮基花青染料作为双环辛炔基化肽标签的荧光探针以及环辛炔基化蛋白质的荧光交联剂。

Bisazide Cyanine Dyes as Fluorogenic Probes for Bis-Cyclooctynylated Peptide Tags and as Fluorogenic Cross-Linkers of Cyclooctynylated Proteins.

作者信息

Demeter Orsolya, Kormos Attila, Koehler Christine, Mező Gábor, Németh Krisztina, Kozma Eszter, Takács Levente B, Lemke Edward A, Kele Péter

机构信息

"Lendület" Chemical Biology Research Group, Institute of Organic Chemistry, Research Centre for Natural Sciences, Hungarian Academy of Sciences , Magyar tudósok krt. 2, H-1117, Budapest, Hungary.

Structural and Computational Biology Unit, Cell Biology and Biophysics Unit, European Molecular Biology Laboratory , Meyerhofstrasse 1, D-69117, Heidelberg, Germany.

出版信息

Bioconjug Chem. 2017 May 17;28(5):1552-1559. doi: 10.1021/acs.bioconjchem.7b00178. Epub 2017 Apr 28.

Abstract

Herein we present the synthesis and fluorogenic characterization of a series of double-quenched bisazide cyanine probes with emission maxima between 565 and 580 nm that can participate in covalent, two-point binding bioorthogonal tagging schemes in combination with bis-cyclooctynylated peptides. Compared to other fluorogenic cyanines, these double-quenched systems showed remarkable fluorescence intensity increase upon formation of cyclic dye-peptide conjugates. Furthermore, we also demonstrated that these bisazides are useful fluorogenic cross-linking platforms that are able to form a covalent linkage between monocyclooctynylated proteins.

摘要

在此,我们展示了一系列双淬灭双叠氮花菁探针的合成及其荧光特性,这些探针的最大发射波长在565至580纳米之间,能够与双环辛炔基化肽结合,参与共价、两点结合的生物正交标记方案。与其他荧光花菁相比,这些双淬灭体系在形成环状染料 - 肽缀合物时显示出显著的荧光强度增加。此外,我们还证明了这些双叠氮化物是有用的荧光交联平台,能够在单环辛炔基化蛋白质之间形成共价连接。

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