发布: 2020年01月20日第10卷第2期 DOI: 10.21769/BioProtoc.3491 浏览次数: 4008
评审: Edgar Soria-GomezBeatrice LiAnonymous reviewer(s)
Abstract
The goal of cryoEM is to determine the structures of biomolecules from electron micrographs. In many cases the processing is straightforward and can be handled with routine protocols. In other cases, the properties and behavior of the specimen require adaptions to properly interpret the data. Here I describe the protocols for examining the higher order assemblies of the retinal adhesion protein, retinoschisin (RS1), using the Bsoft package. The protocols for micrograph preprocessing, 2D classification and 3D alignment and reconstruction follow the usual patterns for the majority of cryoEM specimens. The interpretation of the results is specific to the branched network of RS1 filaments. The 2D class averages are used to determine the relative positions of the RS1 molecules, thus defining the interacting interfaces in the network. The major interface of the linear filament is then further examined by reconstructing the “unit cell” and fitting the molecular models.
Keywords: Electron microscopy (电子显微镜)Background
In cryoEM, the aim is to determine the structures of biomolecules to obtain biologically relevant information. The usual operation is to align, classify and average the 2D particle images obtained from electron micrographs, as well as align and reconstruct these images in 3D. There are several different approaches and many software packages that accomplish these tasks (https://en.wikibooks.org/wiki/Software_Tools_For_Molecular_Microscopy). The one I developed and used here is Bsoft (Heymann, 2001; Heymann and Belnap 2007; Heymann et al., 2008; Heymann, 2018a and 2018c).
In addition to the normal processing protocols, I describe how to approach a specific example, retinoschisin (RS1) (Tolun et al., 2016; Heymann et al., 2019), that exhibits behavior that requires specialized treatment for interpretation (Figure 1A). RS1 forms a network of filaments that adhere to the air-water interface (Figures 1B-1D). Biomolecules typically locate to the air-water interface (Noble et al., 2018; Noble et al., 2019), and often present a preferred orientation that complicates 3D reconstruction. The RS1 molecules in the filaments mainly present only one view. However, these still show many interactions between the individual molecules. Therefore, the strategy is to extract images large enough to contain several RS1 molecules, perform 2D classification and examine the prevalent interaction types (Figure 1A) (Heymann et al., 2019). To deal with the preferred orientation, a partial solution is to process micrographs of 30° tilted specimens to obtain a 3D map of the most common interaction. The 3D reference used here is a “unit cell” containing two RS1 molecules of the linear filament. Two molecules of RS1 are then fitted into the map to examine the interacting residues at their interface.
Figure 1. Protocol scheme and examples of micrographs of RS1. A. The protocol scheme starts with two processing sections common to cryoEM, followed by either 2D classification and averaging or 3D alignment and reconstruction. The results are then interpreted by modeling the interactions between the RS1 molecules. B. A good micrograph, showing a gradient of intensity from the top left to the bottom right. The intensity indicates the specimen thickness, where the lighter parts are thinner and more suitable for particle picking. C. A reasonable micrograph with some ice crystals. The “T” shows a cluster of top views of RS1 located in a somewhat thicker region. D. A micrograph with crystalline ice (“I”) and aggregated RS1 (“A”). Scale bars = 500 Å.
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© 2020 The Authors; exclusive licensee Bio-protocol LLC.
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Readers should cite both the Bio-protocol article and the original research article where this protocol was used:
分类
生物化学 > 蛋白质 > 成像
生物物理学 > 显微技术 > 低温显微镜技术
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