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哺乳动物细胞中一种独特的基因编码荧光共振能量转移对。

A Unique Genetically Encoded FRET Pair in Mammalian Cells.

作者信息

Mitchell Amanda L, Addy Partha Sarathi, Chin Melissa A, Chatterjee Abhishek

机构信息

Department of Chemistry, Boston College, 2609 Beacon Street, 246B Merkert Chemistry Center, Chestnut Hill, MA, 02467, USA.

出版信息

Chembiochem. 2017 Mar 16;18(6):511-514. doi: 10.1002/cbic.201600668. Epub 2017 Feb 9.

Abstract

Förster resonance energy transfer (FRET) between two suitable fluorophores is a powerful tool to monitor dynamic changes in protein structure in vitro and in vivo. The ability to genetically encode a FRET pair represents a convenient "labeling-free" strategy to incorporate them into target protein(s). Currently, the only genetically encoded FRET pairs available for use in mammalian cells use fluorescent proteins. However, their large size can lead to unfavorable perturbations, particularly when two are used at the same time. Additionally, fluorescent proteins are largely restricted to a terminal attachment to the target, which might not be optimal. Here, we report the development of an alternative genetically encoded FRET pair in mammalian cells that circumvents these challenges by taking advantage of a small genetically encoded fluorescent unnatural amino acid as the donor and enhanced green fluorescent protein (EGFP) as the acceptor. The small size of Anap relative to fluorescent proteins, and the ability to co-translationally incorporate it into internal sites on the target protein, endows this novel FRET pair with improved versatility over its counterparts that rely upon two fluorescent proteins.

摘要

两个合适的荧光团之间的荧光共振能量转移(FRET)是监测体外和体内蛋白质结构动态变化的有力工具。对FRET对进行基因编码的能力代表了一种方便的“无标记”策略,可将它们整合到目标蛋白质中。目前,可用于哺乳动物细胞的唯一基因编码FRET对使用荧光蛋白。然而,它们的大尺寸可能导致不利的干扰,特别是当同时使用两个时。此外,荧光蛋白在很大程度上局限于与靶标的末端连接,这可能不是最佳的。在这里,我们报告了在哺乳动物细胞中开发的另一种基因编码FRET对,它通过利用一种小的基因编码荧光非天然氨基酸作为供体和增强型绿色荧光蛋白(EGFP)作为受体来规避这些挑战。与荧光蛋白相比,Anap的小尺寸以及将其共翻译整合到目标蛋白内部位点的能力,赋予了这种新型FRET对比依赖于两种荧光蛋白的同类物更好的通用性。

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