(*contributed equally to this work) 发布: 2015年10月05日第5卷第19期 DOI: 10.21769/BioProtoc.1617 浏览次数: 8992
评审: Fanglian HeRenate Weizbauer
Abstract
Cellulose is a main component of plant cell walls. Tools to analyze cellulose mainly rely on analytical chemistry, which yields information about cellulose amounts and structure, but cannot be applied to intact tissues. Moreover, these methods measure total cellulose and cannot be used to assay cellulose synthesis per se. Live cell imaging of the catalytic subunits of the cellulose synthesis complex (CSC) conjugated to fluorescent proteins is an important tool to understand the dynamics of the cellulose biosynthesis process (Paredez et al., 2006). This method can be used in various genetic backgrounds (Sorek et al., 2014) or with different chemical inhibitors (Brabham and Debolt, 2012). Here we describe in detail the procedure to visualize the movement of CSCs at the plasma membrane. As the movement of CSCs is likely caused by glucan synthesis and extrusion into the cell wall, live cell analysis of CSC velocity provides a method to directly measure cellulose synthesis in vivo.
Keywords: CelluloseMaterials and Reagents
Equipment
Software
Procedure
文章信息
版权信息
© 2015 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Vellosillo, T., Yeats, T. and Sorek, N. (2015). Analysis of in vivo Cellulose Biosynthesis in Arabidopsis Cells by Spinning Disk Confocal Microscopy. Bio-protocol 5(19): e1617. DOI: 10.21769/BioProtoc.1617.
分类
植物科学 > 植物生物化学 > 糖类
植物科学 > 植物细胞生物学 > 细胞成像
细胞生物学 > 细胞成像 > 共聚焦显微镜
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