发布: 2016年09月05日第6卷第17期 DOI: 10.21769/BioProtoc.1919 浏览次数: 19125
评审: Tie LiuYuko KuritaAnonymous reviewer(s)
相关实验方案
基于活性蛋白质组学和二维聚丙烯酰胺凝胶电泳(2D-PAGE)鉴定拟南芥细胞间隙液中的靶蛋白酶
Sayaka Matsui and Yoshikatsu Matsubayashi
2025年03月05日 771 阅读
Abstract
The half-life of a protein is a characteristic property, and can be modulated by post-translational modifications, changes in subcellular localization, and/or interaction with other proteins or ligands. As one determinant of its steady-state level, a protein’s degradation represents an important distinguishing attribute relevant to its biological function. Because protein longevity cannot be elucidated from bioinformatics analyses, it must be determined empirically. Here we describe two approaches for in vivo half-life determination in plants: 1. pooled-seedling degradation assays monitoring either tagged versions of the protein (luciferase fusions or other epitope tags) or following the endogenous protein; 2. single-seedling degradation assays using luciferase fusion proteins. The advantages of these approaches are their simplicity and low cost.
Keywords: Protein degradation (蛋白质的降解)Materials and Reagents
Equipment
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Procedure
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版权信息
© 2016 The Authors; exclusive licensee Bio-protocol LLC.
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分类
植物科学 > 植物生物化学 > 蛋白质
生物化学 > 蛋白质 > 降解
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