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一系列用于植物中蛋白质丰度比例分析的双报告载体。

A series of dual-reporter vectors for ratiometric analysis of protein abundance in plants.

作者信息

Khosla Aashima, Rodriguez-Furlan Cecilia, Kapoor Suraj, Van Norman Jaimie M, Nelson David C

机构信息

Department of Botany and Plant Sciences University of California Riverside CA USA.

Department of Genetics University of Georgia Athens GA USA.

出版信息

Plant Direct. 2020 Jun 21;4(6):e00231. doi: 10.1002/pld3.231. eCollection 2020 Jun.

Abstract

Ratiometric reporter systems enable comparisons of the abundance of a protein of interest, or "target," relative to a reference protein. Both proteins are encoded on a single transcript but are separated during translation. This arrangement bypasses the potential for discordant expression that can arise when the target and reference proteins are encoded by separate genes. We generated a set of 18 Gateway-compatible vectors termed pRATIO that combine a variety of promoters, fluorescent, and bioluminescent reporters, and 2A "self-cleaving" peptides. These constructs are easily modified to produce additional combinations or introduce new reporter proteins. We found that mScarlet-I provides the best signal-to-noise ratio among several fluorescent reporter proteins during transient expression experiments in . Firefly and Gaussia luciferase also produce high signal-to-noise in . As proof of concept, we used this system to investigate whether degradation of the receptor KAI2 after karrikin treatment is influenced by its subcellular localization. KAI2 is normally found in the cytoplasm and the nucleus of plant cells. In karrikin-induced degradation of KAI2 was only observed when it was retained in the nucleus. These vectors are tools to easily monitor in vivo the abundance of a protein that is transiently expressed in plants, and will be particularly useful for investigating protein turnover in response to different stimuli.

摘要

比率报告系统能够比较目标蛋白(即“靶标”)相对于参考蛋白的丰度。这两种蛋白都编码在单个转录本上,但在翻译过程中会分开。这种安排避免了靶标蛋白和参考蛋白由不同基因编码时可能出现的表达不一致问题。我们构建了一组18个与Gateway兼容的载体,称为pRATIO,它们结合了多种启动子、荧光和生物发光报告基因以及2A“自切割”肽。这些构建体易于修饰,以产生更多组合或引入新的报告蛋白。我们发现,在拟南芥的瞬时表达实验中,mScarlet-I在几种荧光报告蛋白中具有最佳的信噪比。萤火虫荧光素酶和海肾荧光素酶在拟南芥中也产生高信噪比。作为概念验证,我们使用该系统研究了卡里金处理后受体KAI2的降解是否受其亚细胞定位的影响。KAI2通常存在于植物细胞的细胞质和细胞核中。在拟南芥中,只有当KAI2保留在细胞核中时,才观察到卡里金诱导的KAI2降解。这些载体是在体内轻松监测植物中瞬时表达的蛋白质丰度的工具,对于研究蛋白质在不同刺激下的周转将特别有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/449f/7306620/070e0bcf97f6/PLD3-4-e00231-g001.jpg

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