拟南芥在轨萌发的蛋白质组学分析方法

Sarahann Hutchinson, Proma Basu, S. Wyatt, D. R. Luesse
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引用次数: 1

摘要

大规模组学方法为国际空间站(ISS)的研究提供了极好的选择,因为它们提供了大量的数据,即使在原始研究完成后也可以继续挖掘。蛋白质组学方法可以提供关于哪些蛋白质被产生、降解或翻译后修饰的信息,潜在地揭示了无法从转录组学数据中辨别的细胞策略。为了从国际空间站上的生物研究罐(BRIC)生长实验中收集足够的组织进行蛋白质组学分析,对现有方案进行了一些修改。每个培养皿固定单元(PDFU)中安置了大约800-1000颗种子。通过将金砖四国从冷停滞转移到室温,这些种子在种植后萌发至120 h。发芽后仅生长72小时,以便有足够的组织进行提取,并尽量减少乙烯和拥挤胁迫的影响。然后将幼苗暴露在RNAlater®中。结果表明,RNAlater®处理的拟南芥幼苗与液氮快速冷冻的拟南芥幼苗产生相同数量的蛋白质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Methods for On-Orbit Germination of Arabidopsis thaliana for Proteomic Analysis
Abstract Large-scale omics approaches make excellent choices for research aboard the International Space Station (ISS) because they provide large amounts of data that can be continually mined even after the original research has been completed. A proteomic approach can provide information about which proteins are produced, degraded, or post-translationally modified, potentially shedding light on cellular strategies that cannot be discerned from transcriptomic data. To collect sufficient tissue from a Biological Research In Canisters (BRIC)-grown experiment on the ISS for proteomic analysis, several modifications were made to existing protocols. Approximately 800–1000 seeds were housed in each Petri Dish Fixation Units (PDFU). These were germinated up to 120 h after planting by transferring the BRIC from cold stasis to room temperature. Growth continued for only 72 h after germination to allow sufficient tissue for extraction, and to minimize the impact of ethylene and crowding stress. Seedlings were then exposed to RNAlater®. Results indicate that RNAlater® - treated Arabidopsis seedlings yield an equal amount of protein to those flash-frozen in liquid nitrogen.
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