发布: 2019年02月20日第9卷第4期 DOI: 10.21769/BioProtoc.3177 浏览次数: 7830
评审: Vamseedhar RayaproluJolene RamseyKristin L. Shingler
Abstract
Advanced labeling technologies allow researchers to study protein turnover inside intact cells and to track the labeled protein in downstream applications. In the context of a viral infection, the combination of imaging and fluorescent labeling of viral proteins sheds light on their biological activity and interaction with the host cell. Initial approaches have fused fluorescent proteins such as green fluorescent protein (GFP) to the viral protein-of-interest. In contrast, self-labeling enzyme tags such as the commercial SNAP-tag, a modified version of human O6-alkylguanine-DNA-alkyltransferase, covalently link synthetic ligands, which users can add on demand. The first two protocols presented here build on previously published protocols for fluorescent labeling in pulse-chase and quench-pulse-chase experiments; the combination of fluorescent labeling with advanced light microscopy visualizes the dynamic turnover of the SNAP-tagged viral protein in intact mammalian cells. A third protocol also outlines how to inspect cellular lysates microscopically for detergent-resistant assemblies of the labeled viral protein. These protocols showcase the flexibility of the SNAP-based labeling system for tracking a viral protein-of-interest in live cells, intact fixed cells, and cell lysates. Moreover, the protocols employ recently developed commercial microscopes (e.g., Airyscan microscopy) that balance resolution, speed, phototoxicity, photobleaching, and ease-of-use.
Keywords: Fusion proteins (融合蛋白)Background
To better understand the role of a viral protein during the infectious life cycle, we have adapted existing strategies that facilitate the determination of intracellular protein location, the assessment of protein dynamics in intact cells, and the continued tracking of the viral protein after lysis of the host cell. The first two protocols build on previously published protocols for on-demand SNAP-labeling and the analysis of protein turnover (Bodor et al., 2012). In previous work, our laboratory has fused a viral protein-of-interest, nonstructural protein 3 (nsP3) of Chikungunya virus (CHIKV), to the SNAP-tag, a modified form of a 20-kDa monomeric DNA repair enzyme (Remenyi et al., 2017 and 2018). During SNAP-labeling, the addition of a synthetic O6-benzylguanine (BG) derivative results in a covalent bond between a reactive cysteine residue in the SNAP-tag and the BG-probe (Keppler et al., 2004a and 2004b).
We have also combined SNAP-labeling with a protocol for inspecting cell lysates via light microscopy, which enables visualization of detergent-resistant protein assemblies. Similar approaches have allowed researchers to detect stable granular assemblies of GFP-tagged stress-granule proteins in cell lysates (Jain et al., 2016; Wheeler et al., 2017). Stress granules are assemblies of RNA and protein (RNPs), which form under conditions of cellular stress (Kedersha et al., 2005). It is now possible to isolate the more stable stress granule core from both yeast and mammalian cells (Jain et al., 2016). SNAP-labeling offers an alternative way of tracking tagged viral proteins that may be present in similar subcellular assemblies. Hence, Protocol 3 may not only be useful to study the biochemical nature of viral proteins but also to track any cellular protein that resides in non-membranous organelles such as RNPs and stress granules. For example, integration of the SNAP-tag into the development of cell lines that produce fluorescently tagged stress granules (Kedersha et al., 2008) could increase experimental flexibility during dynamic and quantitative imaging of these cellular sub-compartments.
Our three protocols also take advantage of recently developed commercial imaging systems for multi-color fluorescence microscopy. We analyze labeled samples in Protocol 1 with live-cell imaging (Figure 1) and thus recommend following general procedures for controlling temperature, reducing phototoxicity, limiting photobleaching, and maintaining cell viability (Frigault et al., 2009). The chosen 2018 Nikon Ti-E2 system allowed us to image a large field-of-view, lessen focus drift with a proprietary Perfect Focus System (PFS), and record multiple positions with the motorized stage. Moreover, illumination with an LED and light exposures not exceeding 1 s allowed for gentler imaging compared to the typical imaging setup of a laser scanning confocal microscope.
For the analysis of labeled protein in Protocols 2 and 3, we chose a confocal imaging setup with proprietary ZEISS Airyscan technology (Figure 1), which is a commercial version of the ‘image scanning microscopy’ approach (Muller and Enderlein, 2010; Sheppard et al., 2013). Airyscan microscopy represents one of the recent innovations in fluorescence super-resolution microscopy, also referred to as nanoscopy (Li et al., 2018). The Airyscan technology improves system resolution with an improved detector design, which features a 32-channel detector array (Huff, 2015). With a new 2D super-resolution mode for Airyscan, this detection approach can now enhance resolution 2-fold while lowering the required fluorescence intensity to obtain high-quality images (Huff et al., 2017). The Airyscan system allowed us to stain our samples with fluorescent dyes from the SNAP product range (e.g., SNAP-Cell® 647-SiR and SNAP-Cell® TMR-Star) and detect them even at low levels during the recovery phase of the quench-pulse-chase protocol. Increased sensitivity also helped in the nanoscopy-based inspection of cellular lysate in Protocol 3 and allowed the visualization of granular structures made up of the SNAP-tagged viral protein. The combination of SNAP-based labeling and innovative detection via Airyscan has the potential to further bioimaging with higher resolution, sensitivity, and user-friendliness.
Figure 1. Overview of experimental protocols. This flowchart outlines the essential steps in Protocols 1, 2, and 3. For the definition of ‘stable CHIKV cells’, see Protocol 1, Procedure section.
Protocol 1: Pulse-chase experiments for long-term imaging with Nikon Ti2-E
Materials and Reagents
Equipment
Software
Procedure
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文章信息
版权信息
© 2019 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Remenyi, R., Li, R. and Harris, M. (2019). On-demand Labeling of SNAP-tagged Viral Protein for Pulse-Chase Imaging, Quench-Pulse-Chase Imaging, and Nanoscopy-based Inspection of Cell Lysates. Bio-protocol 9(4): e3177. DOI: 10.21769/BioProtoc.3177.
分类
细胞生物学 > 细胞成像 > 荧光
细胞生物学 > 细胞成像 > 活细胞成像
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