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Crystal structures reveal transient PERK luminal domain tetramerization in endoplasmic reticulum stress signaling

2015; Springer Nature; Volume: 34; Issue: 11 Linguagem: Inglês

10.15252/embj.201489183

1460-2075

Marta Carrara, Filippo Prischi, Piotr R. Nowak, Maruf M. U. Ali,

Pancreatic function and diabetes

Article29 April 2015Open Access Source Data Crystal structures reveal transient PERK luminal domain tetramerization in endoplasmic reticulum stress signaling Marta Carrara Marta Carrara Department of Life Sciences, Imperial College, London, UK Search for more papers by this author Filippo Prischi Filippo Prischi Department of Life Sciences, Imperial College, London, UK Search for more papers by this author Piotr R Nowak Piotr R Nowak Department of Life Sciences, Imperial College, London, UK Search for more papers by this author Maruf MU Ali Corresponding Author Maruf MU Ali Department of Life Sciences, Imperial College, London, UK Search for more papers by this author Marta Carrara Marta Carrara Department of Life Sciences, Imperial College, London, UK Search for more papers by this author Filippo Prischi Filippo Prischi Department of Life Sciences, Imperial College, London, UK Search for more papers by this author Piotr R Nowak Piotr R Nowak Department of Life Sciences, Imperial College, London, UK Search for more papers by this author Maruf MU Ali Corresponding Author Maruf MU Ali Department of Life Sciences, Imperial College, London, UK Search for more papers by this author Author Information Marta Carrara1,2, Filippo Prischi1, Piotr R Nowak1 and Maruf MU Ali 1 1Department of Life Sciences, Imperial College, London, UK 2Present address: MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK *Corresponding author. Tel: +44 207 594 5733; E-mail: [email protected] The EMBO Journal (2015)34:1589-1600https://doi.org/10.15252/embj.201489183 PDFDownload PDF of article text and main figures. Peer ReviewDownload a summary of the editorial decision process including editorial decision letters, reviewer comments and author responses to feedback. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info Abstract Stress caused by accumulation of misfolded proteins within the endoplasmic reticulum (ER) elicits a cellular unfolded protein response (UPR) aimed at maintaining protein-folding capacity. PERK, a key upstream component, recognizes ER stress via its luminal sensor/transducer domain, but the molecular events that lead to UPR activation remain unclear. Here, we describe the crystal structures of mammalian PERK luminal domains captured in dimeric state as well as in a novel tetrameric state. Small angle X-ray scattering analysis (SAXS) supports the existence of both crystal structures also in solution. The salient feature of the tetramer interface, a helix swapped between dimers, implies transient association. Moreover, interface mutations that disrupt tetramer formation in vitro reduce phosphorylation of PERK and its target eIF2α in cells. These results suggest that transient conversion from dimeric to tetrameric state may be a key regulatory step in UPR activation. Synopsis Activation of unfolded protein response (UPR) upon ER stress involves key regulatory roles of ER-luminal sensor/transducer domains in UPR signaling factors. Structural and functional analyses of the PERK luminal domain reveal a novel tetrameric arrangement, whose transient formation may be an important step in UPR activation. Crystal structure of human PERK luminal domain shows a novel tetramer arrangement. Crystal structure of mouse PERK luminal domain is captured in dimeric form. Biophysical analysis confirm that both mouse and human proteins exist as dimers as well as tetramers in solution. Mutations that disrupt tetramerization in solution reduce phosphorylation of PERK and its target eIF2α in cells. Introduction The unfolded protein response is an important cell signaling system that detects the accumulation of misfolded proteins within the endoplasmic reticulum (ER) and carries out a cellular response that attempts to rectify the imbalance. These responses include transcriptional up-regulation of UPR target genes, global cell translation attenuation, and activation of ER-associated degradation pathways. If the imbalance is not rectified, then the UPR switches from being pro-survival to eliciting an apoptotic response (Zhang & Kaufman, 2008; Hetz et al, 2011; Walter & Ron, 2011). There are three sensor/transducer proteins: Ire1, PERK, and Atf6, that are critical for initiating mammalian UPR cell signaling and give rise to three separate branches of the response. All three proteins have a luminal sensor/transducer domain that in concert with BiP is vital for sensing ER stress, an ER transmembrane region, and a cytosolic domain that propagates the UPR signal (Bertolotti et al, 2000; Schröder & Kaufman, 2005; Ron & Walter, 2007; Zhang & Kaufman, 2008). Crystal structures of yeast and human Ire1 luminal domains have provided a basis for mechanistic understanding of UPR signal activation, although contrasting interpretations of these structures have given rise to differing views on how this occurs (Credle et al, 2005; Zhou et al, 2006; Gardner & Walter, 2011; Walter & Ron, 2011; Korennykh & Walter, 2012; Parmar & Schröder, 2012; Carrara et al, 2013). In an attempt to shed new light upon the mechanism of UPR activation and to rationalize the differences between Ire1 luminal domain structures, we determined the crystal structures of PERK luminal domains in two different states: one state is the previously characterized dimer arrangement as seen with Ire1, and the other state is a novel tetramer arrangement. These two states of PERK were captured using human and mouse luminal domain proteins. The tetramer reveals an interface with the salient feature being a helix swapped between dimers that implies a transient association. Using a combination of biophysical and biochemical techniques, we show that both human and mouse PERK luminal domains form dimers and tetramers in solution, similar to that observed within the crystal lattices. Additionally, PERK mutants reduce tetramer formation in vitro and reduce PERK and eIf2a phosphorylation in cells. These data suggest that transition from luminal domain dimer to transient tetramer state maybe a key step in UPR activation. Results An optimized human PERK luminal domain construct encompassing residues 105–403 was expressed and purified with cleavable N-terminal His-tag in E. coli. This construct was partly identified by sequence and structural similarity to the human Ire1 luminal domain structure (Zhou et al, 2006), but was also observed as a cleavage product from purified full-length luminal domain protein minus the signal sequence. Concurrently, we also expressed and purified mouse PERK luminal domain encompassing residues 101–399 based on the human PERK-optimized construct. We were able to obtain crystals for both human and mouse PERK luminal domain proteins that diffracted to around 3.1Å and 3.3Å at station IO2 at Diamond Light Source, UK (Table 1). Attempts at molecular replacement to obtain phase information were unsuccessful owning to the relatively low sequence identity between Ire1 and PERK luminal domains of 18%. To overcome this, we used a tungsten-derivatized multi-anomalous dispersion (MAD) dataset which yielded a good quality electron density map, from which we were able to build the structure of human PERK luminal domain, and subsequently used this as a molecular replacement model for the mouse PERK luminal domain. The crystal structures reveal human PERK captured in a novel tetramer arrangement, while the mouse PERK luminal domain is visualized in a dimer state similar to Ire1 luminal domains. Table 1. Data collection and refinement statistics H. sapiens M. musculus Peak Na2WO4 Inflection Na2WO4 Remote Na2WO4 – Data collection statistics Space group P41212 P41212 P41212 P3121 Molecules in asym unit 2 2 2 1 Unit cell, a(b),c, Å 83.9, 186.2 84.1,186.5 84.2,186.9 87.6, 73.6 Resolution range, Å 75.6–3.1 76.8–3.57 76.8–4.0 52.8–3.3 Wavelength, Å 1.2148 1.2152 0.9795 0.9795 Completeness, % 99.9(99.5) 99.9(100.0) 99.9(99.8) 99.7(99.7) I/σ(I) 32.3(4.4) 34.6(7.5) 38.5(7.2) 12.2(2.6) Rmerge, % 4.8(65.7) 4.6(42.6) 4.2(36.9) 7.4(63.3) Refinement statistics Protein atoms 3,282 1,268 R work 24.2 28.6 R free 29.3 30.6 Rmsd, Å 0.004 0.003 Rmsd, ° 0.991 0.935 Ramachandran favored, % 91.2 84.1 Ramachandran outliers, % 1.2 2.0 Crystal structure of human PERK luminal domain tetramer The human PERK luminal domain structure forms a ring-type tetramer architecture. The individual monomers are arranged along a twofold rotation axis forming two sets of dimers A–B and C–D. Each dimer presents an inward-facing concave surface that intimately locks together at both ends to create a space in the center of the ring tetramer (Fig 1A and B). The interaction between the dimers is offset relative to each other by 50 degrees. There are two significant interfaces between the monomers that give rise to the dimer and tetramer arrangements (Fig 1C–E). The dimerization interface involves the interaction between monomers A–B and C–D. The interface is slanted by 25° compared to the twofold rotation axis through the middle of the tetramer generating a slightly skewed appearance. This is partly because the monomers within the dimer are not perfectly superimposable resulting in a small degree of asymmetry, but more so because this is an inherent characteristic of the dimer interface as observed for yeast and human Ire1 luminal domain structures. The tetramer interface involves the interaction between monomers A–C and B–D at the opposing side to the dimerization interface. There are substantial contacts between monomers within the tetramer interface, with the key feature being a helix swapped between monomers; such secondary structure swap motifs are indicative of a transient interface (Ali et al, 2006; Czabotar et al, 2013; Tan et al, 2014). Figure 1. Human PERK luminal domain tetramer structure Cartoon representation of human PERK LD tetramer viewed from top along twofold rotation axis with monomer A in orange, monomer B in magenta, monomer C in cyan, and monomer D in green. Top view of human PERK tetramer in molecular surface representation. Side view of tetramer displaying the tetramer interface. Front view of PERK tetramer showing the dimerization interface between monomers. The dimerization interface is offset from the twofold rotation axis by ˜25°. Dimer component of PERK tetramer illustrating the concave surface as viewed from top. Cartoon representation of an individual PERK LD monomer divided into subdomains with red representing dimerization subdomain, blue the β-sandwich subdomain, and yellow tetramer subdomain. Each secondary structural element is numbered. Download figure Download PowerPoint The individual monomers that make up the tetramer consist predominantly of β-strands arranged into β-sheets, with two helices also present. The monomers A and C that come together to form one of the tetramer interfaces are more complete than the corresponding B and D monomers. Residues within monomers A and C are visible from 105 to 400, with the exception of a few loops connecting the secondary structural elements, which are disordered. Monomers B and D have more disorder in regions 300–320 due to the absence of crystal contacts that make up the crystal lattice (Supplementary Fig S1). We have subdivided the luminal domain into three structural motifs related by function: dimerization subdomain, β-sandwich subdomain, and tetramer subdomain (Fig 1F). The dimerization subdomain consists of a series of anti-parallel β-strands that form the dimerization interface between PERK monomers. The central feature of this subdomain is a β-sheet consisting of three long anti-parallel β-strands with β8 forming direct interactions to β8 from the opposing monomer. The "β-sandwich" subdomain consists entirely of β-strands arranged into a two-layer β-sandwich fold that is likely to stabilize the other subdomains. The tetramer subdomain consists mainly of β-strands and one α-helix that come together to create a cleft, which interacts with the opposite PERK monomer in a helix swap that most likely acts to stabilize the transient tetramer interface. Tetramer interface The salient feature of the tetramer interface is the α2 helix being swapped between opposing monomers that results in a total of 2,500 Å of solvent-accessible surface being buried, making this interface more substantial than the dimerization interface. The swapped α2 helix resides in a cleft created by β5–β7 and β18–β19 as part of the tetramer subdomain. The interface comprises predominantly hydrophobic interactions with a number of hydrogen bonds that also contribute to the interface between monomers. The most significant residues that constitute the hydrophobic core are L388, V386, and G389 from β18; L397 and L395 from β19, which together form the base of the cleft; W165 and M172 from β6 and β7, contributing from the top of the cleft (Fig 2A and B). The residues V375, A377, A378, and A381 from the opposing monomer are aligned to one side of the α2 helix that faces into the cleft and constitutes the other part of the core hydrophobic interaction (Fig 2C). Significant hydrogen bond interactions involve the following: N384 and S385, positioned within the base of swapped α2 helix; Y387 and L388, which are found within the β18 forming the bottom of the cleft from one monomer; E170 and M172 from the top of the cleft; and R379 from the swapped helix, respectively. Analysis of sequence alignment between Ire1 and PERK revealed that both the hydrophobic core and hydrogen bonded interactions are conserved, particularly residues located in the two β-strands β18 and β19 that form the base of the cleft (Fig 2D). To further analyze the tetramer interface, we generated a surface electrostatic potential map of our structure. The electrostatic potential of α2 helix is positive while that of the cleft is negative. This clearly indicates a favorable electrostatic potential for interaction between α2 helix and tetramer subdomain cleft (Fig 2E). Figure 2. The novel tetramer interface Residues from PERK monomer that are involved in the tetramer interface. The residues lining the binding cleft and helix α2 are predominantly hydrophobic. Overview of molecular interactions between monomers, colored in cyan and orange, that are involved in tetramer interface. View along the helix α2 shows the hydrophobic core interaction between the swapped helix and the binding cleft. Alignment of PERK and Ire1 sequences from both human and mouse species. The red-colored letters denote functionally conserved residues, with green stars indicating residues involved in hydrophobic core interactions, while blue triangles indicate residues that contribute to the tetramer interface via hydrogen bond interactions. Electrostatic surface potential representation of PERK monomer showing tetramer interface. Download figure Download PowerPoint Crystal structure of mouse PERK luminal domain dimer The crystal structure of mouse PERK luminal domain exhibits a dimer arrangement (Fig 3A and B). The monomer component of the dimer structure is very similar in fold to human PERK with a route mean square deviation (rmsd) value of 1.1 Å when superimposing the two monomer structures together (Fig 3C). The only significant difference between the mouse and human monomer is that in the mouse structure, the tetramer subdomain is disordered. Interestingly, while the mouse structure formed a dimer in the crystal, human PERK, which possesses an ordered tetramer subdomain, is present as a tetramer in the crystal. Figure 3. Mouse PERK luminal domain dimer structure Transparent molecular surface representation of dimeric mouse PERK LD crystal structure, with monomer A colored in red and monomer B in yellow. Mouse PERK monomer organized into three subdomains with dimerization domain in red and β-sandwich domain in blue. The tetramer subdomain is disordered and is not visible within the structure. Structural superimposition of mouse PERK (red) and human PERK (cyan) monomers. The rmsd value between the two monomers is 1.1 Å. Structural superimposition of mouse PERK (red) and human PERK (cyan) dimers, with an rmsd value of 1.0 Å, suggests that the alignment of the dimer interface is consistent between PERK species. Download figure Download PowerPoint Superimposition of the mouse PERK dimer with the dimer component of human PERK tetramer structure again reveals a very close match with an rmsd value of 1.0 Å (Fig 3D). This indicates that the spatial arrangement of the monomers forming the dimer interface is conserved between PERK species. Furthermore, since the dimer interface is present in both dimer and tetramer structures, this suggests that this is a biologically relevant and stable dimer interface. Comparison of PERK and Ire1 luminal domain structures We conducted a search for protein folds that display a homologous structural architecture to PERK in order to gain insights into function using the DALI server (Holm & Rosenstrom, 2010). As expected, we found structural similarities to luminal domains of yeast and human Ire1 only. This suggests that PERK and Ire1 luminal domains form a distinct structural class of proteins likely to have their own function unrelated to other structures within the protein database (PDB). The PERK luminal domain structure displays a similar fold to that of yeast and human Ire1 luminal domains. Structural superposition of human PERK monomer with yeast and human Ire1 indicates rmsd values of 3.8 Å and 4.2 Å. The most significant differences between PERK and Ire1 luminal domains occur at the dimerization interface and swapped α2 helix within the PERK tetramer subdomain. PERK dimerization interface is more substantial than that of human Ire1. It involves a greater number of interactions along β8 with a solvent accessible area of 2,328 Å being buried in PERK, whereas 1,732 Å is buried in human Ire1 interface. In both yeast and human Ire1 structures, the interaction of β8 is less pronounced due to high angle of alignment of monomers resulting in more curved appearance within the dimerization subdomain (Fig 4A). This is compensated for in yeast by binding interactions involving β8 with α1 helix from the opposing monomer resulting in a solvent accessible area of 2,586 Å that is buried in the interface. Similarly, in human PERK, the α1 helix also contributes to the dimerization interface by interacting with β8 from the opposing monomer. Figure 4. Comparison of PERK and Ire1 luminal domains structures Secondary structure comparison of dimerization subdomain interface between PERK and Ire1. PERK dimer interface is greater in area compared to Ire1 due to better alignment of monomers. Structural superimposition of human PERK (cyan) with human Ire1 (red) crystal structures. The α2 helix in PERK structure is projected outwards to form the helix-swapped tetramer interface. The equivalent helix in Ire1 is shorter and projected downward; this orientation is not conducive for helix swap to occur between monomers. The distinctively long helix (αB) observed in Ire1 structure is not present within the PERK structures—a point that is further supported by sequence alignments showing PERK lacking the long helix (αB) region (Supplementary Fig S2), and is not involved in tetramer formation. A section from a structural pairwise alignment between human PERK and yeast Ire1 crystal structures (Supplementary Fig S3) reveals that the only significant stretch of identity (NSVYL-motif) occurs on β18, which forms the base of the cleft within the tetramer subdomain. Download figure Download PowerPoint The PERK-swapped α2 helix is significantly different to that in Ire1 (Fig 4B). The corresponding helix in human Ire1 is shorter and is orientated away from the opposing monomer. The position of α2 helix in Ire1 crystal structure is not conducive for helix swap arrangement between monomers that leads to tetramer formation. The α2 helix is preceded by a distinctively long (αB) helix in Ire1. Within PERK structure, the equivalent long helix segment is disordered and analysis of sequence indicates a low homology between PERK and Ire1 within this region; thus, it is unlikely to form a long helix in PERK. This long (αB) helix is also unlikely to be involved in tetramer formation, and hence, it is not conserved between Ire1 and PERK luminal domains (Supplementary Fig S2). In the yeast Ire1 structure, the α2 helix is disordered, similar to mouse PERK structure. While sequence alignment between human and mouse species of PERK and Ire1 was reliable, we were less confident with yeast Ire1, particularly the C-terminal half of the luminal domain sequence. To identify regions of high similarity between human PERK and yeast Ire1, we conducted a structural pairwise alignment. We found that structural identity within the N-terminal half of the domain was similar to that predicted by sequence alignment, but the C-terminal half was different and revealed a conserved patch (NKVYL yeast Ire1, human PERK NSVYL) that represented the most significant area of structural identity between yeast Ire1 and human PERK (Fig 4C and Supplementary Fig S3). This patch mapped onto β18 within the tetramer subdomain of human PERK and is intimately involved in tetramer interactions. Sequence alignment with human Ire1 had previously identified this region to have a high conservation between species, but was only obvious in yeast Ire1 sequence after structural alignment. Thus, identification of this patch and its position within the tetramer subdomain suggests that tetramer formation and any functional consequence of this event are conserved from yeast Ire1 to human PERK. Small angle X-ray scattering analysis of PERK luminal domain To understand the biological relevance of the human PERK tetramer, we analyzed the oligomeric state of PERK luminal domain in solution. Firstly, we observed that human PERK luminal domain protein eluted from size exclusion chromatography–multi-angle light scattering (SEC–MALS) exclusively as a dimer (Supplementary Fig S4). However, analysis of human PERK luminal domain protein by analytical ultra centrifugation (AUC) revealed a significant tetramer species that exists in equilibrium with dimer in solution, with a dimer to tetramer ratio of 3:2 (Fig 5A). To test whether mouse PERK luminal domain also forms tetramer species, we repeated AUC with mouse PERK luminal domain. We found that mouse PERK luminal domain also forms a dimer–tetramer species that exists in a similar ratio (dim3:2tet) to that of human PERK luminal domain protein (Fig 5B). We did not observe any oligomer species higher than that of a tetramer. This indicates that both human and mouse PERK luminal domains form stable dimers, while the formation of tetramer occurs transiently for both proteins. Furthermore, it suggests that the association and dissociation of stable dimers to form transient tetramers may play a regulatory role in UPR signaling. The ability to crystalize the proteins in different states are purely a result of the crystallization conditions favoring that particular state, and by chance, we were able to capture both states in our crystallization experiments. Next, to confirm that the tetramer arrangement that we visualized within the crystal lattice is present in the same arrangement in solution, we preformed small angle X-ray scattering (SAXS) at concentrations between 1 and 5 mg/ml. We calculated a SAXS profile based on either our human PERK crystal structure tetramer only, our PERK dimer structure only, or a mixture of the two and then compared this to the experimentally derived SAXS solution data profile (Fig 5C). We see a poor fit between calculated and experimental SAXS profiles with both a dimer (χ = 1.7) and tetramer (χ = 1.5) models only. However, when we use a mixture of dimer and tetramer in a ratio of 3:2, as suggested by AUC and reinforced by the SAXS program OLIGOMER (Konarev et al, 2003), we observe an excellent fit between calculated and experimental SAXS profiles (χ = 1.1). This clearly indicates that both the dimer and tetramer arrangements that we see within the PERK crystal structures exist in solution. Moreover, the dimer and tetramer species are in equilibrium similar to that observed by AUC. Thus, we have here captured by X-ray crystallography two biologically relevant states of PERK luminal domain that exists in solution. Figure 5. Small angle X-ray scattering (SAXS) analysis of PERK luminal domain in solution Sedimentation velocity AUC profile reveals human PERK LD exists as a dimer–tetramer species in solution, in a dimer3:2tetramer ratio, indicating the transient nature of the tetramer species, while reinforcing the stable nature of the dimer interface. AUC analysis of mouse PERK LD also indicates that mouse PERK LD forms dimer–tetramer species in a similar ratio (dimer3:2tetramer) to that of human PERK LD. Small angle X-ray scattering analysis of human PERK LD in solution comparing the experimental SAXS profile (gray dots) to the computed profile of PERK LD crystal structures, when using a dimer3:2tetramer ratio of dimer–tetramer, based on AUC and further reinforced by the program OLIGOMER, resulting in an excellent fit (χ = 1.1). Inset, profiles for independent SAXS runs at various concentrations. Download figure Download PowerPoint Structure-guided mutational analysis of PERK tetramer in vitro To further interrogate the biological relevance of the dimer–tetramer states, we introduced mutations into the interface that would affect tetramer formation by specifically targeting hydrophobic interactions. The mutations were as follows: W165A, situated at the top of the hydrophobic cleft; L388N, which forms part of the NSVYL-conserved tetramer patch and is positioned at the bottom of the cleft upon β18; the residues L395N and L397N, located upon β19; and A378N, the conserved residue positioned on the α2 helix, which faces into the hydrophobic core. Mutation of the Leu to Asn replaces a hydrophobic residue with that of a polar, hydrophilic residue of similar size, while mutation of Trp to Ala reduces the hydrophobicity of the residue. Thus, the mutations target the hydrophobic character of the tetramer interface. We employed the use of AUC to measure tetramer formation between wild-type and mutant proteins in solution (Fig 6A). We found that all mutations tested reduced the percentage of tetramer observed in solution when compared to wild-type luminal domain PERK. Mutations positioned at the base of the cleft and on the α2 helix exhibited the greatest effect, reducing the amount of tetramer observed by 52–61% (Fig 6A). Thus, mutations targeting the hydrophobic nature of the tetramer interface reduce PERK luminal domain tetramer formation by shifting the equilibrium in favor of dimer species in solution. Figure 6. Structure-guided mutational analysis in vitro and in vivo Sedimentation velocity AUC analysis comparing the levels of dimer and tetramer in solution between wild-type PERK luminal domain (black) and tetramer interface mutants: W165A (red), L388N (blue), L395N (green), L397N (cyan), and A378N (magenta). All mutations reduce tetramer formation in vitro, with mutations situated at the base of the hydrophobic cleft (L388N, L395N, L397N) and on the helix α2 (A378N) having the greatest effect. PERK−/− MEF cells were transfected with empty vector (EV), myc-tagged wild-type PERK (WT), and myc-tagged PERK tetramer mutants, and were assessed for PERK and eIF2α phosphorylation both in the absence and presence of 5 μm tunicamycin for 4 h to induce ER stress. After immunoblotting, we observed a reduction in the levels of PERK and eIF2α phosphorylation for mutants when compared to wild-type PERK that mirrors the effects seen in vitro. Model illustrating the transition from dimer to tetramer being a likely regulatory step in UPR signal activation. Tetramer formation results in a higher efficiency of auto-phosphorylation of the PERK kinase domain. Source data are available online for this figure. Source Data for Figure 6 [embj201489183-sup-0002-SDataFig6.pdf] Download figure Download PowerPoint Impact of tetramer mutations on PERK stress signaling in vivo To investigate whether tetramer formation is important for PERK signaling in vivo, we transfected PERK−/− cells with empty vector, wild-type PERK, and PERK tetramer mutants: L388N, W165A, L395N, L397N, and A378N and assessed the levels of PERK and eIF2α phosphorylation in the absence and presence of ER stress (Fig 6B). In unstressed cells, there was virtually no PERK phosphorylation observed, as expected. Upon addition of 5 μm tunicamycin to induce ER stress, we observed significant levels of PERK phosphorylation for cells transfected with wild-type PERK, but reduced levels of phosphorylation for all tetramer mutants in comparison. Similarly, we observed negligible levels of phosphorylated eIF2α in unstressed cells; however, we see a clear difference in levels of eIF2α phosphorylation between wild-type and PERK tetramer mutants, with the mutants displaying a reduced level of eIF2α phosphorylation upon addition of ER stress (Fig 6B). These results mirror the effects observed for tetramer mutants for the in vitro analysis experiments. Therefore, these results suggest that luminal domain tetramer formation and specifically the hydrophobic nature of the tetramer interface are important to achieve high efficiency PERK and eIF2α phosphorylation in cells. Discussion In this study, we shed new light on the mechanism of UPR activation by presenting crystal structures of PERK luminal domains captured in two different states. The first dimeric state has been previously described wit