发布: 2019年04月05日第9卷第7期 DOI: 10.21769/BioProtoc.3205 浏览次数: 6261
评审: Amey RedkarGongjun ShiSmita Nair
Abstract
Plant cell walls consist of different polysaccharides and structural proteins, which form a rigid layer located outside of the plasma membrane. The wall is also a very dynamic cell composite, which is characterized by complex polysaccharide interactions and various modifications during cell development. The visualization of cell wall components in situ is very challenging due to the small size of cell wall composites (nanometer scale), large diversity of the wall polysaccharides and their complex interactions. This protocol describes immunogold labeling of different cell wall epitopes for high-resolution transmission electron microscopy (TEM). It provides a detailed procedure for collection and preparation of plant material, ultra-thin sectioning, specimen labeling and contrasting. An immunolabeling procedure workflow was optimized to obtain high efficiency of carbohydrates labeling for high-resolution TEM. This method was applied to study plant cell wall characteristics in various plant tissues but could also be applied for other cell components in plant and animal tissues.
Keywords: Cell walls (细胞壁)Background
Plant biomass is mainly composed of cell walls, which are widely used as an energy source in our daily life (Loqué et al., 2015). At the microscopic scale, cell walls consist of cellulose microfibrils embedded in complex matrix polysaccharides (hemicelluloses, pectins) and structural proteins. Cellulose microfibrils (CMFs) are the largest wall polymers with a radius of 3-5 nm and many micrometers long (Cosgrove, 2005). The orientation of CMFs determines the direction of growth and cell anisotropy (Baskin, 2005), but the CMFs also interact with other wall components all together modifying the wall properties (reviewed in Majda, 2018; Majda and Robert, 2018). The study of cell wall composition has a long history, going back to when different chemicals were applied to bind to the wall composites; however, many of them had a wide range of targets (Wallace and Anderson, 2012; Voiniciuc et al., 2018) and could be observed only via light microscope resolution. In contrast, the immunogold labeling is characterized by a high specificity of antibodies and high-resolution imaging, which can precisely localize the wall epitopes across the wall matrix (e.g., Majda et al., 2017). Despite electron microscopy being a relatively old method, it is not broadly used for plant cell walls. The reason could be that it is time-consuming, requires long training and extensive preparation time. In this protocol, I will walk you through all the steps concerning sample preparation, specificity for all the reagents and troubleshooting.
Materials and Reagents
Equipment
Procedure
文章信息
版权信息
© 2019 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Majda, M. (2019). Visualization of Plant Cell Wall Epitopes Using Immunogold Labeling for Electron Microscopy. Bio-protocol 9(7): e3205. DOI: 10.21769/BioProtoc.3205.
分类
植物科学 > 植物细胞生物学 > 细胞壁
植物科学 > 植物发育生物学 > 形态建成
细胞生物学 > 细胞成像 > 电子显微镜
您对这篇实验方法有问题吗?
在此处发布您的问题,我们将邀请本文作者来回答。同时,我们会将您的问题发布到Bio-protocol Exchange,以便寻求社区成员的帮助。
提问指南
+ 问题描述
写下详细的问题描述,包括所有有助于他人回答您问题的信息(例如实验过程、条件和相关图像等)。
Share
Bluesky
X
Copy link