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通过光亲和标记后修饰在凝集素表面构建用于荧光糖生物传感器的人工信号转导器。

Construction of artificial signal transducers on a lectin surface by post-photoaffinity-labeling modification for fluorescent saccharide biosensors.

作者信息

Nagase Tsuyoshi, Nakata Eiji, Shinkai Seiji, Hamachi Itaru

机构信息

Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, Fukuoka, 812-8581, Japan.

出版信息

Chemistry. 2003 Aug 4;9(15):3660-9. doi: 10.1002/chem.200304925.

Abstract

A new general method, post-photoaffinity-labeling modification (PPALM), for constructing fluorescent saccharide biosensors based on naturally occurring saccharide-binding proteins, lectins, is described in detail. An active-site-directed incorporation of a masked reactive site into a lectin was conducted by using a photoaffinity labeling technique followed by demasking and then chemical modification to yield a fluorescent lectin. Two photoaffinity labeling reagents were designed and synthesized in this study. The labeling reagent with a photoreactive site appended through a disulfide link to a mannoside unit was bound to the saccharide-binding pocket of the lectin concanavalin A (Con A). After light irradiation, the mannoside unit was cleaved by reduction. The unique thiol group thus produced was site-specifically modified with various fluorescent groups (dansyl, coumarin, or dimethylaminobenzoate derivatives) to afford fluorescent Con As. The labeling site was characterized by protease-catalyzed digestion followed by HPLC, MALDI-TOF MS, and tandem mass-mass spectrometry; these methods indicated that the photolabeling step is remarkably site specific. Strong fluorescence was observed in the engineered Con A with a fluorophore, and the emission changed sensitively upon saccharide complexation. The binding constants for various saccharides were determined by fluorescence titration and demonstrated that the binding selectivity and affinity of the engineered Con As are comparable to those of native Con A. The red shift of the emission maximum, the decrease in the fluorescence anisotropy of the dansyl unit, and the increase in the twisted intramolecular charge transfer emission caused by sugar binding to the engineered Con A explicitly indicate that the microenvironment of the appended fluorophores changes from a restricted and relatively hydrophobic environment into a rather freely mobile and hydrophilic environment.

摘要

本文详细描述了一种基于天然存在的糖类结合蛋白(凝集素)构建荧光糖类生物传感器的新通用方法——光亲和标记后修饰(PPALM)。通过光亲和标记技术将一个被掩蔽的反应位点定向引入凝集素的活性位点,随后进行去掩蔽,再进行化学修饰,从而得到荧光凝集素。本研究设计并合成了两种光亲和标记试剂。一种通过二硫键连接到甘露糖苷单元上带有光反应位点的标记试剂与凝集素伴刀豆球蛋白A(Con A)的糖类结合口袋结合。光照后,甘露糖苷单元通过还原作用被裂解。由此产生的独特硫醇基团用各种荧光基团(丹磺酰基、香豆素或二甲基氨基苯甲酸衍生物)进行位点特异性修饰,得到荧光Con A。通过蛋白酶催化消化,随后进行高效液相色谱(HPLC)、基质辅助激光解吸电离飞行时间质谱(MALDI - TOF MS)和串联质谱分析对标记位点进行了表征;这些方法表明光标记步骤具有显著的位点特异性。在带有荧光团的工程化Con A中观察到强烈的荧光,并且在糖类络合时发射发生敏感变化。通过荧光滴定测定了各种糖类的结合常数,结果表明工程化Con A的结合选择性和亲和力与天然Con A相当。发射最大值的红移、丹磺酰单元荧光各向异性的降低以及糖类与工程化Con A结合引起的扭曲分子内电荷转移发射的增加明确表明,所连接荧光团的微环境从受限且相对疏水的环境转变为相当自由移动且亲水的环境。

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