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The eukaryotic group II chaperonin TRiC/CCT is a 16-subunit complex with eight distinct but similar subunits arranged in two stacked rings. Substrate folding inside the central chamber is triggered by ATP hydrolysis. We present five cryo-EM structures of TRiC in apo and nucleotide-induced states without imposing symmetry during the 3D reconstruction. These structures reveal the intra- and inter-ring subunit interaction pattern changes during the ATPase cycle. In the apo state, the subunit arrangement in each ring is highly asymmetric, whereas all nucleotide-containing states tend to be more symmetrical. We identify and structurally characterize an one-ring closed intermediate induced by ATP hydrolysis wherein the closed TRiC ring exhibits an observable chamber expansion. This likely represents the physiological substrate folding state. Our structural results suggest mechanisms for inter-ring-negative cooperativity, intra-ring-positive cooperativity, and protein-folding chamber closure of TRiC. Intriguingly, these mechanisms are different from other group I and II chaperonins despite their similar architecture.
Defects in protein folding are associated with a wide variety of human diseases, including cancer and amyloid diseases such as Huntington's, Parkinson's, and Alzheimer's diseases (Gregersen et al, 2000; Dobson, 2004). The eukaryotic chaperonin TRiC/CCT (TCP1-ring complex or chaperonin containing TCP1) folds ~5–10% of newly synthesized cytosolic proteins, including many essential proteins such as actin, tubulin, and cell-cycle regulators (Rommelaere et al, 1993; Chen et al, 1994; Thulasiraman et al, 1999; Spiess et al, 2004; Yam et al, 2008). The TRiC conformation induced by ATP hydrolysis is closely associated with the productive folding of the substrate (Meyer et al, 2003).
Chaperonins have diverged into two structurally and mechanically distinct families: prokaryotic group I chaperonins such as GroEL–GroES from E. coli (Xu et al, 1997; Bukau and Horwich, 1998) and group II chaperonins, which are further divided into archaeal types (including the thermosome, Ditzel et al, 1998; KS-1, Shomura et al, 2004; and Mm-cpn, Kusmierczyk and Martin, 2003a, 2003b; Reissmann et al, 2007), and the eukaryotic chaperonin TRiC (Frydman et al, 1992). Chaperonin subunits share a common architecture, that is, each consists of three domains (apical, intermediate, and equatorial). Unlike GroEL, which employs an additional cofactor (GroES) acting as a detachable lid (Xu et al, 1997; Bukau and Horwich, 1998), group II chaperonins have a built-in lid formed by a protrusion at the tip of the apical domain of each individual subunit (Ditzel et al, 1998). In addition, GroEL and archaeal chaperonins consist of 1–3 types of subunits, whereas each ring of TRiC contains eight different subunits sharing 27–39% sequence identity (Archibald et al, 2001; Cong et al, 2010). The hetero-oligomeric nature of TRiC implies an inherently asymmetric arrangement among the subunits; however, little is known about how such structural organization is related to its functional activity. Notably, the eukaryotic TRiC has unique functions that the archaeal chaperonins cannot perform, despite their similar architecture. For instance, many TRiC substrates cannot be folded by any other chaperonin (Tian et al, 1995; Frydman, 2001; Hartl and Hayer-Hartl, 2002). This suggests that TRiC must have unique specificity and properties required for maintaining protein homeostasis in the eukaryotic system.
There have been several cryo-EM studies of TRiC in the apo and a variety of nucleotide-containing states (Llorca et al, 1999, 2001; Booth et al, 2008; Cong et al, 2010). The 4Å cryo-EM structure of the closed state suggested a specific model for the 8-subunit arrangement (Cong et al, 2010). Recently, two crystal structures of TRiC bound with tubulin or actin and ATP analogue were reported (Dekker et al, 2011; Munoz et al, 2011) and suggested an alternative 8-subunit arrangement different from the cryo-EM model. Therefore, the true ordering of the eight subunits in TRiC complex remains uncertain.
The present investigation is aimed at determining the quaternary structure changes undertaken by TRiC during its ATPase cycle. We report five cryo-EM maps of TRiC in the apo state and the chemically distinct nucleotide-containing states throughout the ATPase cycle. We did not impose symmetry in the 3D reconstruction process, and unlike other group II chaperonins, this study revealed a surprising degree of asymmetry in the conformation of the open, nucleotide-free state. Our composite structures have revealed a distinct interaction pattern of the 16 TRiC subunits in each of these biochemical states, led to a plausible mechanism of lid closure and could illuminate the positive and negative cooperative phenomena occurring in TRiC upon ATP hydrolysis.
To investigate the structural mechanisms of TRiC conformational transitions during its ATPase cycle (Figure 1), we carried out single particle cryo-EM studies of bovine TRiC in well-defined biochemical states: apo (nucleotide-free), ATP-bound (mimicked by non-hydrolysable ATP analogue AMP-PNP), ADP-bound, and two ATP-hydrolysis transition state analogues induced by ADP-AlFx and ATP-AlFx, respectively (Meyer et al, 2003). Each nucleotide state was obtained by incubation of TRiC with the respective nucleotide analogue and buffer (see Materials and methods).
As the first step of the analysis, we carried out reference-free 2D image analysis on the end-on view images to evaluate whether there is any obvious conformational heterogeneity in each state. TRiC–ADP-AlFx showed two drastically different 2D image patterns, suggesting structural heterogeneity. One has the characteristic appearance of a both-ring open conformation (Supplementary Figure S1A) while the other shows a unique twisted pattern of all the subunits (Supplementary Figure S1B). The 2D images of the other states appeared more homogeneous. Therefore, a multireference refinement procedure in EMAN1 (Chen et al, 2006) was adopted for the TRiC–ADP-AlFx data set, while the standard refinement procedure was applied to the other states.
Since the eight subunits of TRiC are all different, no symmetry was imposed in the reconstruction process for all the five states presented here (Figures 2 and and3),3), allowing us to assess structural differences among the eight distinct subunits. The closed ATP-AlFx state was previously determined at 4.7 Å resolution (Cong et al, 2010), while the resolutions of the other four states were found to be 10.5–13.9 Å (Supplementary Figure S2). This resolution limit can be attributed to preferred particle orientation on the cryo-EM grid, continuous conformational variations, and/or subtle structural heterogeneity in TRiC, which have been found in cryo-EM studies of group II chaperonins (Clare et al, 2008; Zhang et al, 2011).
The end-on view of apo-TRiC reveals an obvious asymmetric pattern among its eight distinct subunits (Figure 2A). However, we cannot determine the subunit identity in this map determined at 10.5 Å resolution. Nevertheless, the structural features of the subunits are distinct enough to annotate them from a1 to a8 for one ring and a′1 to a′8 for the other ring. A cylindrical ‘unwrapping' was applied to the map, and exhibits a pseudo two-fold symmetry between the two rings (Figure 4A). This symmetry was confirmed quantitatively by the rotational correlation analysis between the two rings (Figure 5A). This pseudo two-fold symmetry is located at the inter-ring interfaces between subunits a1 and a′1, and a5 and a′5 (Figure 2A). Therefore, both of the densities (a1 and a′1) should correspond to the same CCT subunit; and the same applies to a5 and a′5. The presence of the pseudo two-fold axis in this symmetry-free reconstruction reinforces our previous observation in the 4.7Å resolution cryo-EM structure of TRiC–ATP-AlFx (Cong et al, 2010). Therefore, the subunit ordering is identical in both rings but arranged in opposite directions as viewed from the side (Figure 4A). Since the question of subunit ordering of TRiC still remains uncertain (Cong et al, 2010; Dekker et al, 2011), we will only refer to the subunits in the complex as a1–a8. Our conclusions are valid for both proposed models, since both agree on the existence of an inter-ring two-fold symmetry axis.
In the apo-TRiC map, both a1 and a′1 subunits display a significantly weaker density than all the other subunits (Figure 4A). This structural characteristic may be caused by the extremely dynamic nature of this subunit as shown in a movie generated from a superposition of a set of reference-free 2D averages of end-on views (Supplementary Movie 1A). Such subunit flexibility is analogous to a large crystallographic B-factor, making a high-resolution structural determination of the apo state impractical (Zhang et al, 2010). Contrary to a1 and a′1, the densities of both a5 and a′5 are better resolved in both rings, and thus more rigid (Supplementary Movie 1A; Figure 2A).
Another characteristic subunit in this apo-TRiC map is a3, which appears to tilt outward from the central chamber (Figure 5B) and lean towards one of its neighbouring subunits (a4), thus separating it further from the other neighbouring subunit (a2) (Figures 4A and and5B).5B). The unwrapped displays (Figure 4) show the relationship between the subunit pairs across the rings, for instance, a3–a′7, a4–a′6 etc. Figure 4A shows that the line between subunit a3 in one ring and subunit a′7 in the other ring has a larger tilt angle and is less parallel (Figure 4A) to the lines joining other subunit pairs (e.g., a2 and a′8).
Based on the above observations, it is tempting to postulate that the conformations of the very dynamic subunit (a1) and/or the outward tilting one (a3) might make them more likely to encounter the substrate proteins in solution and be critical for substrate recruiting of TRiC.
The distinct open conformational states of TRiC occur at essential steps during the folding cycle and facilitate the binding of substrate proteins (Meyer et al, 2003; Reissmann et al, 2007). Here, our maps in the apo, ATP-, and ADP-bound states reveal that the apical domains of TRiC generally extend towards the central chamber in different angles with a slight upward tilt (Figure 2; Supplementary Figure S3A–C). Importantly, akin to the apo and ADP-bound states (Figure 2A and C), our maps clearly demonstrate that TRiC remains open in the ATP-bound state (TRiC–AMP-PNP; Figure 2B). This is consistent with previous biochemical and biophysical studies of TRiC (Szpikowska et al, 1998; Gutsche et al, 2000; Meyer et al, 2003; Reissmann et al, 2007) and recent structural studies on group II chaperonins (Huo et al, 2010; Douglas et al, 2011; Munoz et al, 2011; Zhang et al, 2011). Thus, our observations unambiguously show that nucleotide binding alone is not sufficient to trigger lid closure.
Upon nucleotide binding (AMP-PNP or ADP state), TRiC remains open in both rings similar to the apo state (Figure 2), and a pseudo two-fold symmetry between two rings persists in these conformational states (Supplementary Figure S4). Strikingly, after nucleotide binding the densities of subunits a1 and a′1 appear to be better defined based on the 2D end-on view image analysis (Supplementary Movie 1B and C), and the entire complex appears slightly more symmetrical in 3D (Supplementary Movie 2). These observations are confirmed by the 3D reconstructions, for instance, the missing density corresponding to subunits a1 and a′1 in apo-TRiC is restored in the AMP-PNP and ADP states (Figure 4B and D). Of note, the TRiC–AMP-PNP map demonstrates that the apical domain of subunit a′1 in the bottom ring is less well resolved than its counterpart a1 in the top ring (Figure 4B). This finding indicates that a1 is possibly better poised than a′1 for the lid closure of the top ring, which might require all the subunits in one ring to be more symmetrically arranged. Such asymmetry between a1 and a′1 may reflect the negative inter-ring cooperativity of TRiC (Kafri et al, 2001; Reissmann et al, 2007).
In total, our data reveal that nucleotide binding can cause the subunit to be more rigid and the arrangement to become more symmetric while still open. However, nucleotide binding is not sufficient to close the folding chamber. This mechanism is in strong contrast to group I chaperonins such as GroEL, which undergo their major conformational rearrangement upon binding, not upon hydrolysis of ATP (Xu et al, 1997). This difference could be related to the fact that GroEL has a detachable lid (GroES) to cover the chamber, while TRiC instead has a built-in lid. Hence, the energy needed for chamber closure might be different.
Interestingly, the outward tilt of the subunits a3 and a′3 in the apo state is preserved upon nucleotide binding, as seen in the AMP-PNP state (Figure 5C and F; Supplementary Movie 2). This outward tilting subunit is also seen in the crystal structure of TRiC–ATP-γ-S in complex with tubulin (2XSM) (Munoz et al, 2011). This ATP-bound state (ATP-γ-S) is equivalent to our AMP-PNP state. These two structures match well (Supplementary Figure S5), providing strong evidence for the existence of this unique conformation of TRiC in the ATPase cycle.
All open states display an extra density in the equatorial domain inside the chamber around subunit a6 in one ring and around subunit a′7 in the other ring (indicated by the black arrow in Figure 2). These densities may correspond to the C and N termini (Supplementary Figure S6A), which have also been observed in the 4.7Å resolution TRiC–ATP-AlFx map (Cong et al, 2010; Supplementary Figure S6B).
The characteristic outward tilt of subunits a3 and a′3, the location of the pseudo two-fold symmetry axis, and the extra density in the equatorial domain allowed us to put the structures of these three states in register. Both the self-correlation function for each map (Supplementary Figure S7) and the 2D end-on view movie (Supplementary Movie 1) reveal that the ADP state (Figure 4D), which is the end state of the ATP-hydrolysis cycle and might be the substrate acceptor state, appears to be slightly more symmetrical than the other two states (Figure 4A and B).
TRiC–ADP-AlFx, the trigonal-bipyramidal ATP hydrolysis transition state (Melki et al, 1997), has been demonstrated to represent the physiological substrate folding state (Kafri et al, 2001; Kafri and Horovitz, 2003; Meyer et al, 2003; Reissmann et al, 2007; Douglas et al, 2011). This biochemical state contains a mixture of two TRiC conformations (Supplementary Figure S1A and B). In all, 35% of the data were classified into a conformation with both rings open (Supplementary Figure S1C). The map generated from the remaining data displays an asymmetric conformation with one ring closed (cis-ring) and the other ring open (trans-ring) (Figures 3A and and5D).5D). Using the correlation between this asymmetric TRiC–ADP-AlFx map and the TRiC–AMP-PNP map (Figure 5E), we can register their subunits in both rings (Figure 5G and H). This registration is also apparent in the match of the characteristic outward tilting subunits a3 and a′3 in the two maps (Figure 5G and H).
In the closed cis-ring, we observe a collective inward tilt motion of all eight subunits (Figure 6A; Supplementary Movie 3) and a more symmetrical arrangement relative to all the open states (Figures 2, ,3A,3A, and and5G).5G). The apical domain protruding densities from each subunit come together and have more contacts to form a lid covering the central chamber of the cis-ring. Although the characteristic subunit a3 tilts inwards slightly, it displays relatively less contact with its neighbouring a2 subunit (Figure 5G) and leaves a small opening in the covering lid at the rendering threshold (indicated by black arrow in Figure 3A, and also shown in Figure 3D). Conversely, the apical protruding density of a3 is closer to subunit a4. It is not known if such an arrangement exists in the presence of substrate. If it does, a productive folding of a substrate inside the chamber may not require a complete closure of the lid.
Careful comparison of the closed cis-ring of TRiC–ADP-AlFx with the closed ring of TRiC–ATP-AlFx reveals that on average the chamber of the cis-ring of TRiC–ADP-AlFx is slightly wider (~8 Å) than that of the other state (Figure 3C and D). This expansion results in a volume of ~180 000 Å3 for the closed folding chamber. It has been suggested that group II chaperonins can assist folding of proteins around 40–70 kDa (Spiess et al, 2004; Yam et al, 2008). Such chamber size in TRiC is comparable to that of the closed cis-ring of GroEL–GroES (~175 000 Å3), which can accommodate substrates up to 70 kDa (Xu et al, 1997).
The subunits in the open trans-ring of TRiC–ADP-AlFx exhibit a visible outward tilt motion of the intermediate and apical domains as compared with the AMP-PNP state (Figure 6A). This motion leads to a noticeable chamber enlargement of the trans-ring (Figure 6A), which would be the physiological acceptor state for the next round of substrate and nucleotide binding.
Our cryo-EM maps of TRiC in multiple nucleotide states depict different intra-ring subunit interaction patterns throughout the ATPase cycle. In the open states, the maps reveal contacts among the apical domain in some but not all of the neighbouring subunits (Figure 5B and C). The eight subunits in each ring appear to group into four subunit pairs (a1–a2, a3–a4, a5–a6, and a7–a8) that create a pseudo four-fold symmetry in TRiC, whereby each ring would be formed by a tetramer of dimers. This can be clearly observed especially in the map of TRiC–AMP-PNP (Figure 5C). This pattern of four subunit pairs within a ring might be related to the differential ATP binding and hydrolysis rate among different TRiC subunits (Reissmann, 2007). Upon ATP hydrolysis, the apical-domain interactions among all subunits become more extensive in the closed cis-ring (Figure 3A) and result in shutting the cis-ring chamber (Figure 3A and D).
As for TRiC–ATP-AlFx, a similar intra-ring contacting pattern to that in the cis-ring of TRiC–ADP-AlFx was detected (Figure 3B and D). Interestingly, our map also reveals additional contacts between the apical/intermediate domain of some subunits and its neighbouring equatorial domain, similar to that in the closed thermosome structure (Ditzel et al, 1998). These extra interactions formed in TRiC–ATP-AlFx might be the potential forces making its chamber more compact and even more symmetrical than that of the cis-ring of TRiC–ADP-AlFx (Figures 3B, D, and ((4E).4E). In summary, the apical-domain interaction is maintained or enhanced throughout the ATPase cycle, which suggests its key role in maintaining the association and communication of the TRiC subunits within one ring.
A number of efforts have been made to describe the mechanism of TRiC chamber closure based on cryo-EM studies (Llorca et al, 1999, 2001; Booth et al, 2008). However, this issue remains uncertain because (a) eight-fold symmetry was imposed in their reconstructions and (b) none of these studies included multiple intermediate states. In the present study, we obtained symmetry-free maps of TRiC for four nucleotide-containing states in addition to the apo state. The asymmetrically closed intermediate (TRiC–ADP-AlFx), especially, representing the key physiological substrate folding state, is structurally determined for the first time.
By not imposing symmetry, we uncovered structural details not previously seen in group II chaperonins (Xu et al, 1997; Llorca et al, 1999, 2001; Booth et al, 2008; Clare et al, 2008; Pereira et al, 2010; Zhang et al, 2010). Our analysis clearly shows that the ATP hydrolysis-induced chamber closure motion for each of the subunits is different (Figure 5G; Supplementary Movie 3). A comparison of the subunit arrangement in Figure 4A–E shows a trend of increasing pseudo symmetry during the ATP hydrolysis cycle. The most characteristic and dramatic change is found in the a3–a′7 subunit pair. They may possibly play a critical role in initiating the formation of pseudo symmetry by increasing the extent of apical-domain interactions among all the subunits of that ring. This symmetry would lead to positive cooperativity among subunits in one ring and result in chamber closure of the cis-ring.
Though the motion of each subunit is unique (Supplementary Movie 3), the overall ATP hydrolysis-induced chamber closure motion is similar for each subunit. To demonstrate the motion (Supplementary Movie 4), we use the subunit a5 and a′5 pair as an example, which appear to have minimum motion among the subunits. The cis-ring subunits move ‘upwards' (towards the top of the barrel), and each domain of each subunit tilts inwards with slightly different motions. In the trans-ring subunits, the apical domains move neither downwards nor inwards. Rather, in some of the trans-ring subunits, the apical and intermediate domains tilt outwards (Figure 6A); while the equatorial domains of most trans-ring subunits move radially outward slightly. This outwards motion could prevent the closure of the trans-ring. This opposing motion is a plausible indication of the negative cooperativity of the two rings.
Our characterization of the one-ring closed intermediate TRiC–ADP-AlFx provides some unexpected insights into the structural basis of its negative inter-ring cooperativity. ATP hydrolysis causes a spatial rearrangement at the interface between the two rings, as in the case of GroEL (Xu et al, 1997; Ma et al, 2000). This rearrangement results in an observable increase in separation between the rings in TRiC–ADP-AlFx (Figure 6B; Supplementary Movie 4), while the two major inter-ring contacts are maintained, as in all group II chaperonins (Ditzel et al, 1998). Such a distance increase could reduce the buried surface between the two rings and potentially modify the salt bridges formed between certain opposing subunit pairs (Ditzel et al, 1998), which will vary the interaction network between the rings.
Closely related to the above-discussed subunit a3 and a′7 pair (Figure 4B), our open-state maps reveal that in general if two neighbouring subunits in one ring have formed a pair with contact in the apical domain (e.g., a3 and a4), their connected subunits in the other ring (a′7 and a′6, respectively) tend to be separated in the apical region (Figure 4A and B). This pattern has not been previously observed, and may play a part in both intra- and inter-ring subunit interactions. Such interactions could contribute to the inter-ring negative cooperativity, making TRiC work as a two-stroke molecular machine. This more complex mechanism of inter-ring negative cooperativity of TRiC compared with GroEL is likely related to their different inter-ring interaction patterns, that is, the interactions are registered in TRiC and other group II chaperonins, while it is staggered in GroEL.
Our structures of TRiC reported here show different intra-ring interaction patterns from its archaeal homologue Mm-cpn or prokaryotic homologue GroEL. In the apo state, all these chaperonins share a common neighbouring equatorial-domain interaction within one ring. However, the interactions between the other domains of adjacent subunits vary substantially. In apo-TRiC, we identified apical-domain interactions between pairs of subunits in the same ring (Figures 2A and and4A).4A). Apo-GroEL contains interactions between adjacent apical domains and has contacts between apical and intermediate domains of neighbouring subunits (Supplementary Figure S8A; Braig et al, 1994; Ludtke et al, 2008). In contrast, apo-Mm-cpn has no apical- or intermediate-domain contact in the open state, based on the available symmetric structures (Clare et al, 2008; Pereira et al, 2010; Zhang et al, 2010; Supplementary Figure S8B). This is consistent with the report that the intra-ring cooperativity is relatively weak in archaeal chaperonins, and in the T. acidophilum thermosome it appears to be absent (Bigotti and Clarke, 2005).
These three chaperonins have thus each evolved a different pattern of intra-ring interactions, indicating that the intrinsic inter-subunit coordination strategy is different among them. The enhanced intra-ring subunit contacts seen in TRiC as compared with Mm-cpn may play an important role in stabilizing and specifying the correct assembly of the eight distinct subunits of TRiC; this could also promote a coordinated rotation between the apical and intermediate domains, beneficial for the lid formation from the eight different subunits in TRiC.
The diverse pattern of intra-ring interactions among the open states of TRiC, Mm-cpn, and GroEL (Supplementary Figure S8; Figure 2; Clare et al, 2008; Pereira et al, 2010; Zhang et al, 2010) suggests that different starting points in the chamber closing process lead to differing trajectories of chamber closure. For apo-Mm-cpn, chamber closure appears to involve primarily rigid-body motion of the entire subunit when comparing only two states (Pereira et al, 2010; Zhang et al, 2010) and shows some interdomain movements within a subunit when an additional intermediate state is seen (Zhang et al, 2011). In both TRiC and GroEL, however, the allosteric rearrangement of their lid closure involves relative domain motion within each subunit. However, the direction of the domain motion is different: in TRiC, the apical and intermediate domains move mostly in the same direction (e.g., in subunits a1 and a3, Supplementary Movie 3), while those of GroEL move in the opposite directions (Xu et al, 1997; Booth et al, 2008). In addition, our study depicts a complex inter-ring subunit cooperativity in TRiC (Figure 4), and cross talk between its intra- and inter-ring allosteric networks which may facilitate its chamber closure. Together, the structural mechanism differences in chamber closure among different chaperonins are related to their differences in intra- and inter-ring subunit interaction pattern, with pronounced differences seen in the open conformations.
This study demonstrates how evolution uses a common structural framework but adopts different mechanical switches due to specific gene sequences and consequent allosteric networks. Furthermore, it is possible that the ATPase cycle of chaperonins might be customized to the unique intracellular environments of various organisms or physiological states by interaction with co-chaperones, substrate proteins and perhaps by distinct post-translational modifications (Southworth and Agard, 2008; Tsutsumi et al, 2009).
TRiC was purified from bovine testis essentially as described (Ferreyra and Frydman, 2000; Feldman et al, 2003). In brief, the tubules of bovine testis (500 g) separated from the tunica albuginea by dissection were homogenized in buffer H (20 mM HEPES/KOH (pH 7.4), 5 mM MgCl2, 0.1 mM EDTA, 50 mM NaCl, 1 mM DTT) containing the protease inhibitors leupeptine (2 μg/ml), aprotinin (0.5 μg/ml), pepstatin (0.5 μg/ml) and PMSF (0.2 mM), and the lysate was clarified by centrifugation for 30 min at 20 000 g followed by a 1-h centrifugation step at 100 000 g. The lysate was subjected to a 35% ammonium sulphate cut, and the resulting supernatant was precipitated with a final concentration of 50% ammonium sulphate. The pellet was resuspended in a small volume of MQ-A buffer (20 mM HEPES/KOH (pH 7.4), 5 mM MgCl2, 0.1 mM EDTA, 50 mM NaCl, 10% glycerol, 1 mM DTT) and 30 ml aliquots, respectively, were loaded on sucrose cushions (lower layer: 2 ml 60% sucrose in MQ-A buffer; upper layer 5 ml 20% sucrose in MQ-A buffer). After 20 h ultracentrifugation in a SW-28 rotor at 26 000 r.p.m. and 4°C, the sucrose cushions together with all sedimented materials were pooled, dialysed against MQ-A buffer, and loaded on a Q Sepharose FF column (60 ml, GE Healthcare, USA) equilibrated in MQ-A buffer. Bound proteins were eluted with 0.4 M NaCl in MQ-A buffer. Fractions containing proteins were pooled and diluted 1:1 in MQ-A buffer before they were loaded on a High-Trap Heparin column (20 ml, GE Healthcare, USA) equilibrated in MQ-A buffer containing 0.2 M NaCl. Bound proteins were eluted by a NaCl gradient ranging from 0.2 to 1 M NaCl. Fractions containing TRiC were pooled, concentrated using an Amicon Ultra-15 10K concentrator (Millipore Corporation, USA), and loaded on a Superose 6 10/300 GL column (GE Healthcare). Fractions containing the oligomeric chaperonin were pooled, and aliquots were flash frozen in liquid nitrogen.
TRiC samples were prepared for cryo-EM studies by dilution of purified TRiC to 0.5 mg/ml. The TRiC sample was proven to be folding active under our freezing conditions by an actin refolding assay (Meyer et al, 2003). Nucleotide-free samples were frozen immediately. TRiC–ATP-AlFx/TRiC–ADP-AlFx samples were incubated in the presence of 1 mM ATP/ADP, 5 mM MgCl2, 5 mM Al(NO3)3, and 30 mM NaF for 1 h at 30°C prior to freezing. For TRiC–ADP/TRiC–AMP-PNP, the sample was incubated in the presence of 1 mM ADP/10 mM AMP-PNP and 5 mM/15 mM MgCl2 for 15 min at 30°C prior to freezing. Since commercial AMP-PNP typically contains impurities (Meyer et al, 2003), we performed purification on it by anion exchange chromatography as described (Horst et al, 1996). In all, 3 μl of sample was deposited onto a glow-discharged 400/200 mesh Quantifoil holy carbon grid (1.2 × 1.3 μm hole size, Quantifoil Micro Tools GmbH, Jena Germany). The grid was flash frozen in liquid ethane using a Vitrobot (FEI, Hillsboro, OR, USA). Data were recorded on a JEM 3200FSC microscope (JEOL, Tokyo) equipped with a field-emission gun operated at 300 kV and an in-column energy filter (using 20 eV slit). The spot size was set to 1; the condenser and objective aperture were set to 50 and 120 μm, respectively. Specimen temperature was maintained at 101 K. Images were recorded at × 50 000 microscope magnification on Kodak SO-163 films with the specimen dose of 18 electrons/Å2. The images were digitized on a Nikon Super CoolScan 9000 ED scanner with 6.35 μm/pixel scanning interval.
The particles were boxed out from digitized micrographs by boxer from EMAN 1.8 (Ludtke et al, 1999, 2001) and e2boxer.py from EMAN2 (Tang et al, 2007). CTF parameter estimation was carried out using the EMAN1 program ctfit. Reference-free 2D analysis was carried out using refine2d program in EMAN1 (Ludtke et al, 1999, 2001). For the ADP-AlFx state, there are two conformational states that coexist based on the 2D image analysis (Supplementary Figure S1A), so that multirefine procedure in EMAN1 as described previously (Chen et al, 2006; Booth et al, 2008) was employed. All the 3D reconstructions using EMAN1 were completed with no symmetry imposed. In addition, a recently developed 2D fast rotational matching (FRM2D) algorithm (Cong et al, 2003, 2005; Cong and Ludtke, 2010), available in EMAN 1.8+, was adopted in the final refinement. This method has been used to obtain a number of subnanometer resolution cryo-EM maps (Cong et al, 2009, 2010). Micrographs with a defocus range of ~1.2–3.5 μm were used in the final reconstruction process. For each of the five states, the particle number included in the final 3D reconstruction was listed in Supplementary Figure S2A. Except for the closed ATP-AlFx state (4.7 Å; Cong et al, 2010), the resolutions of the rest of the four states are assessed to be in the 10.5–13.9 Å resolution range based on the 0.5 cutoff for the Fourier Shell Correlation (Saxton and Baumeister, 1982; Harauz and van Heel, 1986).
The existence of the one-ring closed asymmetric conformation induced by ATP hydrolysis is validated by our reference-free 2D image analysis and 3D reconstruction. First, the 2D image analysis of TRiC–ADP-AlFx particles depicts a unique end-on view in which all the subunits appear twisted (Supplementary Figure S1B), not seen in any of the other four states. If the two rings were in the same conformation, there would be no handedness in the end-on projection of TRiC as seen here. The twisted pattern is comparable to computed projections of the true bullet-shaped GroEL–Aacpn10–ADP complex (Chen et al, 2008), as well as a simulated asymmetric map (composed of a closed ring from TRiC–ATP-AlFx and an open ring from apo-TRiC). Moreover, our 3D reconstruction using multirefine in EMAN1 (Chen et al, 2006) indicates that the majority of TRiC particles (~65%) in this data set adopt the one-ring closed conformation (and were used in the reconstruction of the map shown in Figure 3A), while the remainder is in the conformation with both rings open (Supplementary Figure S1A and C), similar to the other open conformations of TRiC. The above analyses clearly confirm the existence of this asymmetric intermediate of TRiC in the ATP hydrolysis transition state (mimicked by ADP-AlFx).
To interpret the structural mechanism in more detail, a pseudo atomic model for each state was generated. We first built a homology model of the TRiC complex in the closed state (TRiC–ATP-AlFx). Since the current reconstructions were completed at relatively low resolution, we began with a homology model corresponding to the CCT2 subunit using thermosome (1A6D) as template and fit it as rigid body to all the subunits in the closed TRiC–ATP-AlFx map. In order to fit the closed-state model of the entire TRiC complex to each of the maps in different biochemical states, we used the real-space refinement/sampling program DireX (Schroder et al, 2007, 2010). DireX uses a geometrical sampling approach to flexibly fit a model into the density map in an iterative manner while ensuring correct stereochemistry and non-overlapping atoms. The model of the closed state was first placed into the density map of apo-TRiC using CHIMERA (Pettersen et al, 2004). Strong elastic restraints were used to avoid overfitting the density. The restraints were chosen between randomly chosen atoms that are within a distance range of 3–15 Å and that are separated by not >100 residues along the protein chain. The number of restraints was chosen as two times the number of atoms. The fitted model of apo-TRiC then served as the starting point for the refinements of other states. For the fitting, 500 optimization steps were performed with DireX, which took on average about 7 h on a single cpu (Intel Nehalem 2.93 GHz). In all refinements, a restrained grouped occupancy refinement was used, which adapted the contribution of the residues to the model density. This was done to account for reduced or missing density. This, however, adds only a small shift to the global position and orientation of the individual subunits and has almost no influence on the local structure. Finally, the models were subjected to minimization with CNS (Brunger, 2007). As shown in Supplementary Figure S3, these models fit to the corresponding density maps well particularly for equatorial and intermediate domains. Our models do not include some regions of the apical domain in several subunits, for example, in apo-TRiC, because the map in those regions was not very well resolved due to the dynamic nature of those subunits. However, such models are useful and simplified to represent the structural complexity and variations of TRiC in the ATPase cycle.
The density maps are deposited to EMDB (accession numbers EMD-1960, EMD-1961, EMD-1962, and EMD-1963) and the associated models are deposited to PDB (PDB IDs: 4A0O, 4A0V, 4A0W, and 4A13). They will be released upon publication.
We thank Dr John F Flanagan IV for the help in composing the map unwrapping tools. This research is supported by grants from NIH through the Common Fund (PN1EY016525), NIGMS (GMR01-074074), and National Center for Research Resources (P41RR002250).
Author contributions: YC, JF, and WC designed research; ASM and SR prepared the specimen and defined the biochemical conditions for attaining different states; YC and JJ collected the cryo-EM data; YC carried out all the image processing and map analysis with the advice of SJL and MFS, and BM involved in the data preprocessing; YC and GFS built the models; YC, MTD, and WC generated the movies; YC, ASM, MFS, JF, and WC interpreted the structures; YC, GFS, ASM, MFS, SR, ML, SJL, JF, and WC wrote the paper.
The authors declare that they have no conflict of interest.