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高亲和力和扩展动态范围的红色荧光 cAMP 指示剂。

Red fluorescent cAMP indicator with increased affinity and expanded dynamic range.

机构信息

Department of Optical Imaging, The Institute of Biomedical Sciences, Tokushima University Graduate School, 3-18-15 Kuramoto-cho, Tokushima City, Tokushima, 770-8503, Japan.

Department of Biomolecular Science, Toho University, 2-2-1 Miyama, Funabashi, 274-8510, Japan.

出版信息

Sci Rep. 2018 Jan 30;8(1):1866. doi: 10.1038/s41598-018-20251-1.

Abstract

cAMP is one of the most important second messengers in biological processes. Cellular dynamics of cAMP have been investigated using a series of fluorescent indicators; however, their sensitivity was sub-optimal for detecting cAMP dynamics at a low concentration range, due to a low ligand affinity and/or poor dynamic range. Seeking an indicator with improved detection sensitivity, we performed insertion screening of circularly permuted mApple, a red fluorescent protein, into the cAMP-binding motif of PKA regulatory subunit Iα and developed an improved cAMP indicator named R-FlincA (Red Fluorescent indicator for cAMP). Its increased affinity (K = 0.3 μM) and expanded dynamic range (860% at pH 7.2) allowed the detection of subtle changes in the cellular cAMP dynamics at sub-μM concentrations, which could not be easily observed with existing indicators. Increased detection sensitivity also strengthened the advantages of using R-FlincA as a red fluorescent indicator, as it permits a series of applications, including multi-channel/function imaging of multiple second messengers and combinatorial imaging with photo-manipulation. These results strongly suggest that R-FlincA is a promising tool that accelerates cAMP research by revealing unobserved cAMP dynamics at a low concentration range.

摘要

环化变异 mApple 是一种红色荧光蛋白,我们将其插入蛋白激酶 A 调节亚基 Iα 的环化 AMP 结合基序中,进行插入筛选,由此开发出一种改良的环化 AMP 指示剂,命名为 R-FlincA(环化 AMP 的红色荧光指示剂)。其亲和力增加(Kd=0.3 μM)和动态范围扩大(pH7.2 时为 860%),使得能够检测到亚微摩尔浓度下细胞中环化 AMP 动态的细微变化,而现有指示剂则难以观察到这些变化。检测灵敏度的提高也增强了 R-FlincA 作为红色荧光指示剂的优势,因为它可以实现一系列应用,包括多个第二信使的多通道/功能成像以及与光操作的组合成像。这些结果强烈表明,R-FlincA 是一种很有前途的工具,它通过揭示低浓度范围内未被观察到的环化 AMP 动态,加速了环化 AMP 研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c27f/5789972/7168d3c2685d/41598_2018_20251_Fig1_HTML.jpg

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