Protein bodies: how the <scp>ER</scp> deals with high accumulation of recombinant proteins

Protein bodies (PBs) are highly specialized protein storage organelles in cereal seeds. PB formation in seeds initiates in the endoplasmic reticulum (ER), and depending on the plant species, PBs remain in the ER or find their way out of the ER, bypass the Golgi and end up in protein storage vacuoles (PSVs) (Khan et al., 2012). Protein bodies have been ectopically induced in leaves by producing high amounts of ER-retrieved recombinant proteins, usually by fusing them to protein tags such as Zera®, elastin-like polypeptide (ELP) and hydrophobin-I (HFBI). PBs induced by these processes are numerous, round and clustered, they remain in the ER, and they are not destined to the central vacuole (Llop-Tous et al., 2010; Saberianfar et al., 2015, 2016). The simultaneous monitoring of recombinant protein accumulation and PB formation suggested that a recombinant protein threshold of 0.2% total soluble protein is required for PB formation (Figure 1A). This observation was based both on expression of fluorescent proteins in transgenic tobacco lines (Gutiérrez et al., 2013), and on transient expression of fluorescent proteins as well as nonfluorescent xylanases in Nicotiana benthamiana (Saberianfar et al., 2015). Although fusion tags are not necessary for PB formation, their presence affects the distribution pattern and size of PBs (Saberianfar et al., 2015). This can be due to their physicochemical properties. Indeed, all three types of fusion tags possess hydrophobic regions, which enable fusion tags and their fusion partners to self-assemble into aggregates and facilitate the process of PB formation. Once PBs arise, they grow in size over time (Figure 1B), reaching their maximum size at 5 days post infiltration (dpi) for GFP-ELP and GFP-HFBI (Saberianfar et al., 2015), and at 10 dpi for Zera®-ECFP (Llop-Tous et al., 2010). In all cases, PB growth is accompanied by an increase in accumulation levels of the respective recombinant protein. Once PBs start forming, they can trap endogenous and other co-expressed proteins. Indeed, PBs were shown to contain ER-specific proteins such as BiP, calreticulin and calnexin (Conley et al., 2009; Joseph et al., 2012). As a result, other proteins of interest can be trapped into PBs when co-expressed with PB-inducing proteins. For instance, GFP targeted either for secretion or for retrieval to the ER was sequestered into PBs upon co-expression with RFP-HFBI or RFP-ELP. Also, co-expression of valuable and low-accumulating proteins such as erythropoietin and interleukin-10 with GFP-HFBI led to increased accumulation of both proteins (Saberianfar et al., 2015). Such proteins are likely sequestered in PBs where they are prevented from progressing through the secretory pathway, and over time, their concentration in PBs increases (Figure 1B). This PB-trapping strategy is important for two reasons; it helps to increase accumulation levels of difficult-to-express recombinant proteins and eliminates the need for the addition of fusion tags which might affect the proper folding and activity of the protein of interest. This strategy, however, does not work as well with Zera®, because the strong affinity of Zera® molecules to one another results in a condensed and sticklike alignment of Zera® molecules which excludes other molecules from the core of PBs (Llop-Tous et al., 2010). This was confirmed with co-expression of secretory GFP or ER-targeted GFP with Zera®-DsRed in which the GFP signal localized to the periphery of Zera® PBs and not in their core, and explains why Zera®-DsRed has no significant effect on EPO accumulation (Saberianfar et al., 2016). Previous studies on PBs have interpreted the subcellular localization of PBs differently. Zera®-induced PBs were described as highly dense aggregates, which remain connected to the lumen of the ER rather than forming independent organelles (Llop-Tous et al., 2010). Alternatively, ELP and HFBI PBs were described as terminally stored organelles, which bud off the ER and are highly mobile in the cytosol (Joensuu et al., 2010). We recently showed that physical connections exist between PBs induced by ELP, HFBI and Zera® using a new GFP photoconversion technique (Sattarzadeh et al., 2015). Confocal imaging of connections between PBs using fluorescent proteins is technically challenging. PBs induced by fluorescent proteins generally appear extremely bright under the confocal microscope due to the accumulation of high levels of fluorescent proteins in their lumen. Therefore, high-quality imaging is only possible under excitation with low laser power and minimal gain. In these conditions, the ER network connecting PBs, which contains low amounts of the fluorescent proteins, is not visible. Due to these technical difficulties, photoconversion is an important tool to monitor the movement of proteins between PBs and allows imaging of protein trafficking out of and into PBs. Based on our observations, in the case of ELP and HFBI, photoconverted proteins within PBs were rapidly transferred, first to surrounding PBs (Figure 1C,D), and then to distant PBs within the cell via the ER (Figure 1E). In the case of Zera®, protein movement between PBs was also observed, but was much slower, likely due to covalent disulphide bridges between Zera® molecules leading to large aggregates (Saberianfar et al., 2016). These results indicate that PBs are linked to each other through the ER and that PBs are not terminally stored cytosolic organelles. Another technique to show the connection of PBs is transmission electron microscopy (TEM). For a TEM image to capture PB connections, it is critical that the specimen be sectioned at a focal plane that shows these connections similar to what was shown by Hofbauer et al. (2014). As sample preparation is a random process, in many cases PB connections are not visible. The ideal technique to capture the details of PB connections would be electron tomography that can provide 3D images based on multiple sections of a cluster of PBs. In higher plants, ER formation and movement are actin-dependent via interaction of actin microfilaments with myosin XI proteins. The movement of PBs induced by Zera®, ELP and HFBI fusion tags was disrupted by the use of Latrunculin B, an actin depolymerizing drug, and ELP-induced PBs were shown to lose mobility in the presence of a mutant myosin XI-K tail. Furthermore, PBs form and align along actin strands and are surrounded by an ER membrane (Conley et al., 2009; Saberianfar et al., 2016). Therefore, we speculate that PBs remain connected to the ER, and move along the ER network which relies on the actin cytoskeleton for movement (Figure 1). It is not fully clear whether high accumulation of proteins causes the formation of PBs or whether the formation of PBs is responsible for accumulation of high amounts of recombinant proteins. We believe reaching a certain protein accumulation in the ER is critical in PB initiation, and other factors such as presence or absence of the fusion tags contribute to PB maturation. Understanding the mechanism of PB formation will help us use this technology for increasing the yield of foreign proteins in plant expression systems. The differences between the fusion tags and how they direct their fused partner to PBs need further investigation. We showed that all three types of PBs arise from the ER, but that Zera®-induced PBs do not co-localize with either ELP- or HFBI-induced PBs. Unlike ELP and HFBI, Zera® does not require an ER retrieval signal to accumulate in the ER and form PBs. It is possible that Zera®-induced PBs originate from a different subdomain of the ER compared to ELP- or HFBI-induced PBs. This can be examined for instance by co-expression with ER subdomain-specific proteins. Although PBs induced by fusion tags show differences, this feature might be useful for simultaneous expression of different proteins in vivo and their targeting into the same or separate PBs, especially as Zera®, ELP and HFBI can be isolated and purified by different purification strategies. Even though it is clear that all fusion-induced PBs exchange their contents through the ER, we cannot rule out the potential role of de novo protein synthesis by ribosomes attached to the rough ER membrane of Zera®-, ELP- and HFBI-induced PBs. This question can be addressed by a photoconversion-based FRAP experiment in the presence and absence of an inhibitor of protein synthesis (e.g. cycloheximide), in which fluorescence recovery is measured. In conclusion, induction of PB formation enables the storage of high amounts of intracellular recombinant proteins without imposing excessive stress to the ER, and may be a coping mechanism that eukaryotic cells have evolved to prevent ER stress and cell death. We believe that PBs work as extensions of the ER and provide sufficient space for protein accumulation. Taking advantage of this phenomenon can constitute an approach to addressing the production bottleneck of low recombinant protein accumulation levels in plants, especially in leaf-based expression systems. We thank Alex Molnar for assistance with preparation of the model. This work was supported by AAFC A-base project 1725 to RM. RS was supported by an NSERC postdoctoral visiting fellowship. The authors declare no conflict of interest.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.