Rational mutagenesis to support structure-based drug design: MAPKAP kinase 2 as a case study
- Maria A Argiriadi1, 2Email author,
- Silvino Sousa1, 3,
- David Banach1, 2,
- Douglas Marcotte1, 4,
- Tao Xiang1, 5,
- Medha J Tomlinson1, 3,
- Megan Demers1, 6,
- Christopher Harris1, 2,
- Silvia Kwak1, 2,
- Jennifer Hardman1, 2,
- Margaret Pietras1, 3,
- Lisa Quinn1, 7,
- Jennifer DiMauro1, 5,
- Baofu Ni1, 3,
- John Mankovich1, 8,
- David W Borhani1, 9,
- Robert V Talanian1, 2 and
- Ramkrishna Sadhukhan1, 3
© Argiriadi et al; licensee BioMed Central Ltd. 2009
Received: 23 September 2008
Accepted: 18 March 2009
Published: 18 March 2009
Structure-based drug design (SBDD) can provide valuable guidance to drug discovery programs. Robust construct design and expression, protein purification and characterization, protein crystallization, and high-resolution diffraction are all needed for rapid, iterative inhibitor design. We describe here robust methods to support SBDD on an oral anti-cytokine drug target, human MAPKAP kinase 2 (MK2). Our goal was to obtain useful diffraction data with a large number of chemically diverse lead compounds. Although MK2 structures and structural methods have been reported previously, reproducibility was low and improved methods were needed.
Our construct design strategy had four tactics: N- and C-terminal variations; entropy-reducing surface mutations; activation loop deletions; and pseudoactivation mutations. Generic, high-throughput methods for cloning and expression were coupled with automated liquid dispensing for the rapid testing of crystallization conditions with minimal sample requirements. Initial results led to development of a novel, customized robotic crystallization screen that yielded MK2/inhibitor complex crystals under many conditions in seven crystal forms. In all, 44 MK2 constructs were generated, ~500 crystals were tested for diffraction, and ~30 structures were determined, delivering high-impact structural data to support our MK2 drug design effort.
Key lessons included setting reasonable criteria for construct performance and prioritization, a willingness to design and use customized crystallization screens, and, crucially, initiation of high-throughput construct exploration very early in the drug discovery process.
Structure-based drug design (SBDD) can be an effective contributor to the identification and optimization of drug candidates by providing a structural rationale for the design of improved compounds. Protein crystallization, structure determination, and the rapid determination of multiple protein/ligand complexes can be expensive and time-consuming. Major variables include protein construct design, mutations, and post-translational modifications, the nature of protein impurities (chemical or conformational), the choice of ligands or even proteins for co-crystallization, and the crystallization conditions themselves. These variables represent an enormous matrix of experimental possibilities that is difficult or impossible to explore systematically. Despite these challenges, the availability of structural information at the preliminary stages of a drug discovery program is critical to maximize impact. Therefore, efficient methods developments, techniques and strategies to deliver structures early in a project are clearly needed.
MAPKAP kinase 2 (MK2) plays a key role in the production of pro-inflammatory cytokines such as TNF-α. MK2 is activated by the mitogen-activated protein (MAP) kinase p38 [1–3]. Activated MK2 phosphorylates a number of target proteins in immune cells resulting in cytokine production and cellular proliferation and activation. Mice lacking MK2 are healthy and fertile, but they fail to increase production of pro-inflammatory cytokines such as TNF-α, IL-6, and IFN-γ  in response to stimuli such as lipopolysaccharide. MK2 knockout mice are resistant to the development of collagen-induced arthritis, a model for human rheumatoid arthritis . The catalytic activity of MK2 is required to mount the pro-inflammatory response . These and related studies have attracted attention to MK2 as a target for the design of therapeutic treatments for rheumatoid arthritis and other TNF-α-driven diseases.
Although the data supporting MK2 as a promising drug target have been available for nearly ten years, to our knowledge there are no MK2 inhibitors in clinical development. Many companies have initiated MK2 projects, but little success has been reported. Anecdotally, a common problem has been that high-throughput screening for lead MK2 inhibitors has been unproductive. We believe SBDD targeting MK2 could help address this issue. Yet, despite several reports of MK2 crystal structures at moderate (2.7–3.8 Å) resolution [7–10], the routine production of well-diffracting MK2 crystals bound to compounds of diverse structure remains difficult. More robust methods are needed to enable efficient SBDD.
The domain structure of MK2 may contribute to these difficulties . Its proline-rich N-terminal domain (residues 1–65) is unique, having no counterpart in other MAP kinases . This domain binds c-ABL Src homology 3 domain in vitro . The sequence of the kinase domain (66–327) identifies MK2 as a Ser/Thr kinase family member. MK2 exhibits low homology to other Ser/Thr kinases, however, with the exception of the close homologs MK3 and MK4. The regulatory domain at the C-terminus (328–400) contains an autoinhibitory α-helix [7, 8] followed by nuclear export signal (NES) and nuclear localization signal (NLS) sequences [2, 3, 12–15]. The NES and NLS are essential for MK2 complex formation with p38 and subsequent translocation to the nucleus. Deletion of the entire MK2 regulatory domain results in a marked increase in catalytic activity . There are three critical phosphorylation sites on MK2: Thr222, Ser272, and Thr334 [16, 17]. Phosphorylation at these residues activates MK2 by causing a conformational change in the C-terminal regulatory α-helix: on kinase activation, the helix displaces from the kinase surface and thereby allows substrates to bind [7, 9, 16].
Construct design is known to be a critical factor in producing large quantities of soluble protein and reproducible crystals. For example, it can be difficult to predict precisely domain boundaries and to identify the surface residues of globular proteins, alteration of which might enhance solubility or crystallization. Altering or deleting features such as surface hydrophobicity, post-translational modifications, side-chain flexibility, secondary structural elements, or even entire domains can dramatically modulate protein physical characteristics, especially solubility. Protein solubility also depends on details such as the expression vector, host cell, culture conditions, and protein fusion partner used. To increase crystallization robustness and improve crystal diffraction, we thought such wide-ranging approaches needed to be explored with MK2.
Here we report the optimization of several steps in human MK2 structure determination: rapid and systematic exploration of construct design and expression screening; high-throughput protein purification; and wide screen crystallization with customized factorial grids. Our methods expand upon those of Malawski et al. , who examined only N- and C-terminal truncations of the MK2 catalytic domain. We took advantage of the fact that MK2 is one of the few kinases that expresses well in Escherichia coli, which facilitates high-throughput construct design and production, to explore the effect of not only truncations but also two kinds of surface mutations and several internal deletions.
Our strategy had four components: First, the N- and C-termini of the protein were varied. Second, surface-exposed lysine and glutamate residues with high conformational entropy  were mutated to drive novel crystallization contacts and thereby enhance crystallization. Third, internal flexible regions were deleted, again to foster novel crystal forms. Fourth, phosphorylation sites [16, 17] were altered to provide homogenous MK2 rather than a heterogeneous mixture of unactivated (no phosphorylation) and activated (partial or full phosphorylation) forms.
We implemented a high-throughput, parallel approach to enable construct production, expression, and purification of all mutants within a short time, nearly all of which expressed well and were tested in customized, kinase-specific robotic crystallization screens. The methodological improvements implemented here enabled the screening of 44 MK2 constructs, resulting in seven crystal forms, diffraction testing of ~500 crystals, and high-resolution data collection and structure determination of ~30 MK2/inhibitor complexes.
Results and discussion
Representative MK2 expression constructs.
N- and C-terminal variations
Entropy-reducing surface mutations
MK2(41–364, K343A, E344A)
MK2(47–366, E88A, K89A)
Activation loop deletions
MK2(41–364, T222E, T334E)
MK2(47–366, T222E, T334E)
Construct Design Strategy
Our initial construct design tactic was alteration of the N- or C-termini of full-length MK2, thereby either removing flexible terminal segments that might hinder crystallization or simply providing different termini that might enable different crystal forms (via altered packing, isoelectric point, hydrophobicity, etc.). This approach has been used previously by several groups, and limited systematic N- and C-terminal truncations have been explored ; the construct used most often has been MK2(41–364), a form of the enzyme noted to be constitutively-active . Given the poor behavior of the early constructs that included (part of) the proline-rich N-terminal domain, we deleted this domain in all subsequent constructs. We explored several termini: Gln41, His47, and Arg50; and Gln327, Leu342, Asp345, Thr357, Arg364, Asp366, and His400 (Figure 1). These residues delineate the kinase domain at the N-terminus, and the kinase domain, the autoinhibitory α-helix, and the NES/NLS at the C-terminus.
Our second tactic addressed the protein physical characteristic of surface entropy. Following Longenecker and colleagues , a series of point mutants was designed to alter flexible surface lysine and glutamate residues to minimize crystal protein entropy and entropic loss on crystallization. This approach was successfully used with RhoGD1, for which new crystal forms were identified that exhibited enhanced diffraction. Several MK2 mutants in which alanine was substituted for lysine or glutamate are shown in Table 1 (see also Figure 1 and Additional File 1 Table S7). All mutants were constructed at one time, without iterative improvements.
Our third tactic addressed the internal flexibility of MK2. In several of the prior MK2 structures, the kinase activation loop (residues 220–238) engages in significant crystal contacts. We hypothesized that deletion of this long, flexible loop (Figure 1) might drive formation of alternate, better-diffracting crystal lattices. We thus examined two activation loop deletions: MK2(41–364, ΔL220-G238) and MK2(47–366, ΔL220-G238).
Our final tactic sought to reduce the chemical and conformational heterogeneity of MK2. All reported MK2 structures are of the unphosphorylated enzyme. Previous studies had shown that mutation of phosphothreonine residues to glutamate led to constitutive activation of the kinase [16, 17]. We reasoned that by altering the activation state of the protein, we would not only access a more homogeneous enzyme but also distinct conformational states, and hence increase the likelihood of useful crystal forms. The pseudoactivated mutants were based on two truncated constructs, MK2(41–364) and MK2(47–366). Glutamate mutations T222E and T334E (both singly, and as the double mutant) replaced the threonines reported to activate MK2 when phosphorylated. We prioritized mutation of T222 and T334 over S272 because existing data suggested that the threonine residues were the more significant MK2 phosphorylation sites . T334 is shown in Figure 1; T222 is located within the disordered portion of the activation loop.
Expression, Purification and Crystallization
Solubility assessment for representative MK2 constructs.
K343A, K344A, K364A
Summary of pseudoactivated MK2 construct expression, enzymatic activity, and crystallization.
Enzymatic Activity (cts/nM)
Without p38 activation
With p38 activation
Customized MK2 robotic crystallization screen conditions.
7.0 – 8.5
Seven MK2 crystal forms.
Crystallization Conditions *
Unit Cell (a, >b, c, Å)
Res. (Å) N†
MK2(41–364) & MK2(47–366) surface mutants ‡
AS, LS, & NP
Rods; high mosaicity
MK2(41–364) & MK2(47–366) surface mutants ‡
AS, LS, & NM
Plates; high mosaicity
2 M AS
0.1 M Na citrate
2 M NM
10 μM Anapoe 80
Bipyramids; inhibitor soaking req'd
1.5–1.8 M NM
Hex. bullets; co-crystals
1.5–1.8 M NM
Hex. bullets; co-crystals; "collapsed" Form V
1.75 M AS
0.1 M Na citrate
Sharp blocks; co-crystals
Crystallographic statistics for an MK2/lead compound inhibitor complex.
Unit cell length (a; Å)
⟨ I/σ I ⟩
Data completeness (%)
Pseudoactivated MK2 adopts the conformation of inactive MK2
For reasons that are still unclear, MK2 has an overwhelming propensity to make specific, trimer-forming intermolecular contacts as it crystallizes. Some of our mutations abrogated these contacts; instead of shifting crystallization to new conditions and crystal forms, however, those MK2 constructs simply did not crystallize. Thus, a level of mutagenesis that would be sufficient for most proteins of this size was surprisingly less effective with MK2.
What are these trimers? As noted by Hillig et al. , two distinct packing interactions are present in both Form IV (space group F 4132; PDB entry 2JBO) and Form VII (P 212121; PDB entry 2JBP) MK2 crystals (Table 5). The Type 1 trimer is mediated by a draping of the N-terminus, beginning around residue 47, over the N-lobe of another MK2 subunit. Constructs beginning at residues 41 or 47 retain this contact and crystallize; those beginning at residue 50 lose the contact and do not form crystals. The Type 2 trimer is mediated by the C-terminal portion of the activation loop packing against helices F, G, and H. Constructs in which the activation loop was deleted, being unable to form these contacts, do not crystallize. Notably, Glu233-Arg313 and Glu238-Arg280 salt bridges mediate Type 2 contacts. Targeting of these glutamate residues in a second round of entropy-reduction mutagenesis might have altered the Type 2 contacts enough to spur formation of other crystal forms.
MK2 trimer formation is due entirely either to crystallographic symmetry (Form IV) or to non-crystallographic symmetry (Form VII). Form IV has one molecule/asymmetric unit, and the two types of trimers are formed by adjacent, non-intersecting crystallographic 3-fold symmetry axes. Conversely, since space group P 212121 has no 3-fold axes, the 12 molecules/asymmetric unit in Form VII are arranged such that both trimer types are formed by two non-crystallographic 3-fold axes that nearly intersect in the center of the 12-subunit, virus-like MK2 shell.
Amazingly, all characterized MK2 crystal forms shown in Table 5 are composed of Type 1 and/or Type 2 trimers. Forms V and VI (both P 63; e.g., PDB entry 1NXK) have four molecules/asymmetric unit; three subunits form the Type 1 non-crystallographic trimer; the fourth, "odd man out" subunit forms, through crystallographic symmetry, the Type 2 trimer. And, the tenuous packing in Form III (P 213; four molecules/asymmetric unit, 78% solvent) is mediated by trimer formation at two adjacent, non-intersecting crystallographic 3-fold axes, as in the other cubic (Form IV) crystal form. Only the first reported MK2 structure (R 3; PDB entry 1KWP; two molecules/asymmetric unit) breaks the pattern . Uniquely compared to all other MK2 crystals, the construct used in that study included the complete MK2 C-terminus. Packing in this crystal form is mediated by the Type 1 trimer (crystallographic 3-fold) and a novel (parallel, crystallographic) trimeric contact centered at residue 370 that positions the extended C-terminus (ordered to residue ~385) to pack against another MK2 subunit.
Although the biological relevance of MK2 trimer formation is unknown, we note that trimer formation is structurally incompatible with formation of the MK2-p38 complex [23, 24]. Thus, MK2 trimer formation may be a form of self-regulation relevant in vivo.
In summary, much of the mutagenesis work reported here was, in the end, stymied by the unusually strong proclivity of MK2 toward trimer formation. Nonetheless, our systematic approach did indicate that truncations rather than mutations were more effective for MK2 crystallization. The exact position of the MK2 N-terminus is more important than is the C-terminus, and the activation loop could not be deleted. Surface arginine and glutamate residues drive crystallization more strongly than do surface lysine residues prevent it. The pseudoactivation constructs were helpful, likely due to slight modulation of protein surface properties rather than by producing a different protein conformation. These unusual MK2 properties result in many closely related (though at first glance apparently different) crystal forms (Table 5). Additional surface mutants (including untargeted glutamates, and also arginines) would seem to be required to drive MK2 into truly different crystal forms that can be produced under low ionic strength (e.g., polyethylene glycol) conditions rather than in high salt.
The systematic methods for the design, production and evaluation of MK2 protein constructs presented here allowed us to reproducibly obtain suitable crystals such that structure-based drug design could proceed. Our methods are robust and allowed rapid evaluation of about fifty constructs. This rapidity enabled the scale-up production of selected MK2 constructs in multi-milligram quantities proteins for structural studies. Using rational site-directed mutagenesis and in-house customized crystallization screens (Table 4), we were able to identify several novel crystallization conditions. Combined with variation of other parameters, such as surface side chain entropy and (pseudo)activation state, these high-throughput techniques produced five new MK2 crystal forms, most with improved diffraction characteristics (Table 5). One such crystal form, grown with a MK2 phosphorylation-site pseudoactivation mutant, was used to solve our first MK2/lead inhibitor complex (Figure 5).
Several key lessons were learned from this exercise. First, setting reasonable criteria for construct performance and prioritization is essential to identify constructs suitable for further evaluation and possible scale-up. In the case of MK2, most constructs gave satisfactory performance in expression and purification. Choices were necessary, however; we prioritized higher-yielding, more soluble constructs (Table 2) for scale-up and more extensive crystallization screening. Implicitly, we assumed that constructs that expressed or purified poorly were less likely to crystallize well. Our assumption appears to be supported by the expression yield, protein melting point, and crystallization data of Malawski et al. . Second, a systematic crystallization screen (Table 4; see also Additional File 1 Table S8) was required to identify crystallization conditions in a robust manner. Indeed, the interplay between multiple constructs and multiple, customized crystallization solutions likely contributed greatly to our success. We note that the composition of customized crystallization screens is protein-specific – for MK2, we used a preponderance of high ionic strength conditions, since repeated screening with, for example, PEG solutions never provided crystals. Other proteins will behave differently. Third, reduction of surface side chain entropy can require several iterative rounds before productive mutation sites are identified. In retrospect, more than one round of surface residue mutations in this study, optimally informed by initial structural information, might have yielded additional crystal forms (e.g., mutation of Glu233 and Glu238 to disrupt the Type 2 trimer contact). Fourth, high throughput construct exploration must be initiated early in a drug discovery program in order to synchronize with hit-to-lead synthetic chemistry efforts, preferably in concert with initial target selection studies, i.e. before a high-throughput inhibitor screen is begun. This head start is especially critical for problematic crystallization targets like MK2. Applying these lessons learned from our experience with MK2 has helped us to accelerate many other structural programs, enabling us to impact lead discovery programs more rapidly and efficiently.
Most human MK2 http://www.expasy.org/uniprot/P49137 constructs were engineered as fusion proteins with Schistosoma japonicum glutathione S-transferase (GST; http://www.expasy.org/uniprot/P08515), using the pGEX4T-1 vector (GE Healthcare). The sequence used was: GST-(SDLVPR↑GSENLYFQ↑G)-MK2. The linker sequence encodes thrombin and tobacco etch virus (TEV) protease cleavage sites ("↑"). Two protease sites were included for maximal flexibility in removal of the fusion tag after purification; we almost exclusively used the TEV protease site, resulting in an unnatural glycine residue N-terminal to MK2. A few constructs were also made as His6-FLAG-TEV-MK2 fusion proteins, using the pET21a+ vector (Invitrogen). The sequence used was: (MGHHHHHHGSGDYKDDDDKDYDIPTTENLYFQ↑G)-MK2. We refer to these vectors as "pGEX4T-1-GST-Thr-TEV" and "pET21a+-His6-FLAG-TEV", respectively.
Mutagenic primers were designed according to the QuikChange XL Site-Directed Mutagenesis Kit (Stratagene) instructions and were purchased from Invitrogen. Briefly, primer pairs were made for each mutation. Both primers in each pair contained the desired mutation and annealed to the same sequences on opposite strands of the plasmid template. The desired mutations (nucleotide replacements or deletions), in the middle of each primer, were flanked by 15–19 bases of wildtype sequence on both sides. Primer stocks and dilutions were arrayed in 96-well V-bottom microplates (MJ Research) and stored at -20°C.
Site-directed mutagenesis was performed using the QuikChange kit (Stratagene) using the plasmids pGEX4T-1-GST-Thr-TEV-MK2(47–366) and pGEX4T-1-GST-Thr-TEV-MK2(41–364) as templates. PCR was performed in 96-well V-bottom microplates using a DNA Engine Dyad (MJ Research) thermocycler complete with an ALS-1296, 96-well alpha unit (MJ Research). Reaction mixtures were cycled 18 times according to this schedule: 95°C, 50 s; 60°C, 50 s; 68°C, 14 min. Cycling was preceded by incubation at 95°C (1 min) and followed by incubation at 68°C (7 min).
Transformation of XL-10 Gold Ultracompetent E. coli cells (Stratagene) was performed in 24-well RB Blocks (Qiagen). Thawed cells (45 μL) were mixed on ice with 2 μL of 2-mercaptoethanol in each well. A 5 μL aliquot of each PCR reaction mix was added to the appropriate well and the mixture was incubated on ice for 10 min. The blocks were then heat-shocked by immersing the lower half of the blocks into a 42°C water bath (30 s), then placing the block back on ice (2 min). SOC medium (0.5 mL; preheated to 42°C) was then added to each well and the block was immediately placed in an incubator at 37°C for 1 hr with shaking. A 0.1 mL aliquot of each transformation was spread onto 100 mm LB agar plates containing 100 μg/mL ampicillin and incubated overnight at 37°C.
Plasmid DNA was prepared using the QIAprep 8 Turbo Miniprep Kit (Qiagen) in combination with the Qiavac 6S vacuum manifold (Qiagen) according to manufacturer's instructions. The DNA was quantitated spectrophotometrically and diluted to 100 μg/mL with water for sequence analysis. The coding sequence of all constructs was verified.
Plasmids encoding the MK2 constructs were transformed into BL21 (DE3) strain for expression studies. Competent cells were transformed with 0.5 μL of each plasmid in 24-well blocks as above (without 2-mercaptoethanol). The transformation mix (0.1 mL) was spread onto 100 mm LB agar plates containing 100 μg/mL ampicillin and incubated overnight at 37°C. Starter cultures grown at 37°C were used to inoculate 2.5 mL of LB medium containing 100 μg/mL ampicillin in 24 deep-well blocks. Once an OD600 of 0.4–0.6 was reached, the blocks were shifted to 18°C for 1 h and then induced with IPTG (0.4 mM) for 4 h. Cells were harvested by centrifugation, frozen at -80°C. Large-scale cultures were induced in the same way with the exception that the flasks were shifted to 4°C for 40 min prior to induction.
Analysis of the soluble and insoluble fractions was performed by SDS-PAGE on 4–20% gels (Invitrogen). Cells were thawed and resuspended for lysis in Bug Buster HT (Novagen; 0.25 mL per unit OD600). Bugbuster HT containing 60 kU rLysozyme (Novagen; 0.1 mL) was added to the cell suspension (0.1 mL). The mixture was incubated on ice for 15 min before addition of 0.2 mL of Bugbuster HT containing 20 mM DTT and Complete, EDTA-free Protease Inhibitor cocktail (Roche; 1 tablet/30 mL Bugbuster HT). An aliquot of the crude lysate was separated by centrifugation; the supernatant was analyzed as the soluble fraction. The pellet was resuspended in an equal volume of BugBuster HT and analyzed as the insoluble fraction. Proteins were visualized with SimplyBlue stain (Invitrogen)
Western blotting was used to confirm protein identity. Gels were transferred to PVDF membranes using a Protean II Mini Trans-Blot apparatus (BioRad). After blocking membranes with 5% nonfat dry milk in TBS-T buffer (50 mM Tris·HCl, pH 8.0, 150 mM NaCl, 0.1% Tween-20), the blot was probed with horseradish peroxidase-conjugated anti-GST antibody diluted 1:1000 in TBS-T/5% nonfat milk. Membranes were washed extensively with TBS-T, and then bound antibodies were visualized using the SuperSignal West Pico chemiluminescent substrate kit (Pierce).
MK2 variants were purified using the following procedure at 4°C: Cell pellets were thawed and resuspended in lysis buffer containing 50 mM Tris·HCl, 250 mM NaCl, 10% glycerol, 1 mM DTT, 1 mM EDTA, pH 7.5. The cell suspension was sonicated on ice for 20 s iterations and then centrifuged (22,000 × g) for 45 min. A 10 mL glutathione affinity column (GE Healthcare) was prepared by washing with ten column volumes of Buffer A (50 mM Tris·HCl, 250 mM NaCl, 10% glycerol, 2.5 mM DTT, 1 mM EDTA, pH 8.0) containing Complete, EDTA-free Protease Inhibitor cocktail. Soluble cell lysate was applied to the column and then extensively washed with Buffer A. MK2 was eluted from the column with Buffer A + 40 mM glutathione. The GST tag was cleaved using TEV protease, typically 4–16 h at 4–15°C. The sample was then diluted ten-fold with Buffer B (50 mM MES, 10% glycerol, pH 6.0) and loaded onto a MonoS 10/10 column (GE Healthcare) equilibrated with Buffer B + 20 mM NaCl. The protein was eluted at ≈200 mM NaCl using a stepwise Buffer B/NaCl gradient. MK2-containing fractions were pooled and concentrated to 10 mg/mL, and then loaded onto a Superdex 75 16/60 column (GE Healthcare) equilibrated with 50 mM Tris·HCl, 250 mM NaCl, 10% glycerol, 1 mM DTT, pH 7.5; protein was eluted at 1 mL/min. MK2-containing fractions were pooled and sample purity was assessed by SDS-PAGE; protein identity was confirmed using mass spectrometry.
Enzymatic assays utilized a homogeneous time-resolved fluorescence method (CisBio-US, Inc.) to quantitate product formation. Reactions contained in 40 μL: varying amounts of enzyme, 4 μM peptide substrate (Biotin-Ahx-AKVSRSGLYRSPSMPENLNRPR), 10 μM ATP, 20 mM MOPS, 10 mM MgCl2, 5 mM EGTA, 5 mM 2-phosphoglycerol, 1 mM Na3VO4, 0.01% Triton X-100, 5% DMSO, 1 mM DTT, pH 7.2. After 60 min at room temperature, reactions were quenched by adding 10 μL of 0.5 M EDTA. Phosphorylated peptide was measured by addition of 75 μL of 24 ng/mL Eu3+-cryptate-labeled anti-phospho-14-3-3 binding motif (CisBio-US, Inc.), 1.47 μg/mL SureLight™ allophycocyanin-streptavidin (CisBio-US, Inc.), 50 mM HEPES, 0.1% BSA, 0.01% Tween-20, 0.4 M KF. The developed reaction was incubated in the dark at room temperature for 10 min, then read in a time-resolved fluorescence detector (Perkin Elmer Discovery or BMG Rubystar) at 620 nm and 665 nm simultaneously, using a 337 nm nitrogen laser for excitation. The 665/620 emission ratio is proportional to the amount of phosphorylated peptide product. Since the HTRF method does not provide absolute quantities of product formed, specific activities were calculated as HTRF counts/nM MK2 protein.
MK2 constructs yielding more than 1 mg/L of culture were progressed to crystallization trials. Protein was concentrated to 10 mg/mL using an Ultrafree-15 Biomax 10 kDa molecular weight cut-off centrifugal filter device (Millipore). Various inhibitors were added individually to concentrated protein stocks to a final concentration of 1 mM. Complexed MK2 protein (0.5 μL) was mixed with 0.5 μL of various crystallization solutions from Crystal Screen 1™ and Crystal Screen 2™ (Hampton Research) and Wizard Screen 1™ and Wizard Screen 2™ (DeCode Biostructures). The resulting drops were dispensed into 96-well sitting drop trays (Greiner) using a Hydra II+1 liquid handler (Thermo Scientific Matrix). Trays were stored at 18°C and visualized manually. Crystallization was tested extensively at 4°C, uniformly without success.
Accumulated MK2 crystallization hits suggested parameters to be explored more closely in a customized robotic screen, the most effective being the precipitating reagent and pH range. A complete 96-well screen, designed for use with the Hydra II+1, consisted of four 4 × 6 grid screens: (1) (NH4)2SO4/sodium citrate, pH 7–8.5; (2) sodium malonate, pH 7–8.5; (3) sodium phosphate; pH 7–8.5; and (4) a randomized screen obtained by randomly mixing the above three precipitants with other additives (Table 4; see also Additional File 1 Table S8). Seven different crystal forms were identified from this comprehensive screen, as shown in Table 5 and Figure 4.
Crystals for inhibitor soaking were grown in sitting drops by the vapor-diffusion method using MK2(47–366, T222E). MK2 (1.5 μL, 10 mg/mL) was added to 1.5 μL of reservoir solution (2 M sodium malonate, pH 5.5, and 0.01 mM Anapoe 80 [Hampton Research]) and then the drop was sealed in vapor contact with 500 μL of reservoir solution. Crystals grew to about 0.2 mm in size in 3 days. For soaking, one MK2 crystal was added to 60 μL of 1 mM inhibitor dissolved in mother liquor and incubated at 18°C overnight.
Diffraction Testing and Structure Determination
MK2/inhibitor complex crystals were harvested into a cryoprotectant solution (20% glycerol plus mother liquor) using a fiber loop and flash-cooled in liquid nitrogen. Cystals were stored in liquid nitrogen until diffraction testing. X-ray diffraction testing was conducted in-house using a FR591 rotating anode generator (Bruker AXS) with a MAR345 image plate detector (MARResearch) and Osmic optics (Rigaku USA). A total of 535 crystals were tested, and over 80 crystals were selected for synchrotron data collection if diffraction reached at least 3.5-Å resolution. Advanced Photon Source (Argonne, IL) and National Synchrotron Light Source (Upton, NY) synchrotron beamlines were used primarily for data collection, although a few crystals were selected for in-house data collection.
Diffraction data was processed with the HKL2000 program suite . After determining the crystal orientation, the data were integrated with DENZO, scaled and merged with SCALEPACK, and placed on an absolute scale and reduced to structure factor amplitudes with TRUNCATE . Five percent of the unique reflections were assigned, in a random fashion, to the "free" set, for calculation of the free R-factor (Rfree) ; the remaining 95% of reflections constituted the "working" set, for calculation of the R-factor (Rcryst). The x-ray diffraction data for a representative inhibitor-soaked MK2 crystal (Form IV) are summarized in Table 6.
The CCP4 program suite was used to solve and refine the structure . The cross-rotation function was calculated using MOLREP , using the apo MK2 structure reported previously (Protein Data Bank entry 1KWP; ) as the search model. Initial coordinates were generated based on the one solution apparent at 2.9 Å resolution. Refinement began with rigid-body refinement in REFMAC , resulting in an Rcryst of 37.0% (Rfree 40.0%) for all reflections with |F| > 2.0σ F , 20–2.9 Å. Manual rebuilding of the model was conducted using the molecular graphics program O  and examination of sigmaA-weighted 2FO-FC and FO-FC electron-density maps . Restrained refinement using REFMAC converged at an Rcryst of 22.9% (Rfree 26.8%), 20–2.9 Å. The quality of the model was assessed with PROCHECK  and WHATCHECK .
We thank Vincent Stoll and Kenton Longenecker (Abbott Laboratories) for helpful discussions regarding construct design, comments on the manuscript and assistance in data collection at APS. We also thank Eric Goedken (Abbott Bioresearch Center) for comments on the manuscript.
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