crystallization communications\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

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ISSN: 2053-230X

Crystallization and preliminary crystallographic studies of the copper-binding domain of the amyloid precursor protein of Alzheimer's disease

aBiota Structural Biology Laboratory, St Vincent's Institute, 9 Princes Street, Fitzroy, Victoria 3065, Australia, bDepartment of Pathology, The University of Melbourne, Victoria 3010, Australia, cThe Mental Health Research Institute of Victoria, Parkville, Victoria 3052, Australia, and dCentre for Neuroscience, The University of Melbourne, Victoria 3010, Australia
*Correspondence e-mail: wmckinstry@svi.edu.au

(Received 7 September 2004; accepted 15 November 2004; online 2 December 2004)

Alzheimer's disease is thought to be triggered by production of the amyloid β (Aβ) peptide through proteolytic cleavage of the amyloid precursor protein (APP). The binding of Cu2+ to the copper-binding domain (CuBD) of APP reduces the production of Aβ in cell-culture and animal studies. It is expected that structural studies of the CuBD will lead to a better understanding of how copper binding causes Aβ depletion and will define a potential drug target. The crystallization of CuBD in two different forms suitable for structure determination is reported here.

1. Introduction

Alzheimer's disease is a debilitating disorder confronting ageing populations worldwide. It is increasingly accepted that Alzheimer's disease is brought about by an increased production of the amyloid β (Aβ) peptide, which is neurotoxic and compromises neuronal function (Selkoe, 2002[Selkoe, D. J. (2002). Science, 298, 789-791.]). The peptide arises through the cleavage of the amyloid precursor protein (APP; Kang et al., 1987[Kang, J., Lemaire, H. G., Unterbeck, A., Salbaum, J. M., Masters, C. L., Grzeschik, K.-H., Multhaup, G., Beyreuther, K. & Muller-Hill, B. (1987). Nature (London), 325, 733-736.]) by the sequential cleavage of β-site APP-cleaving enzyme (BACE) and the protein complex γ-secretase. APP is a type I transmembrane protein with a large extracellular portion and may play a role in signalling (see, for example, Cao & Sudhof, 2001[Cao, X. & Sudhof, T. C. (2001). Science, 293, 115-120.]) or interaction with the extracellular matrix (Rossjohn et al., 1999[Rossjohn, J., Cappai, R., Feil, S. C., Henry, A., McKinstry, W. J., Galatis, D., Hesse, L., Multhaup, G., Beyreuther, K., Masters, C. L. & Parker, M. W. (1999). Nature Struct. Biol. 6, 327-331.]).

APP is able to bind Cu ions (Hesse et al., 1994[Hesse, L., Beher, D., Masters, C. L. & Multhaup, G. (1994). FEBS Lett. 349, 109-116.]) and can modulate the level of copper ions in the brain by transporting the ions in and out of neurones (White et al., 1999[White, A. R., Reyes, R., Mercer, J. F. B., Camakaris, J., Zheng, H., Bush, A. I., Multhaup, G., Beyreuther, K., Masters, C. L. & Cappai, R. (1999). Brain Res. 842, 439-444.]; Maynard et al., 2002[Maynard, C. J., Cappai, R., Volitalis, I., Cherny, R. A., White, A. R., Beyreuther, K., Masters, C. L., Bush, A. I. & Li, Q. X. (2002). J. Biol. Chem. 277, 44670-44676.]; Bellingham et al., 2004[Bellingham, S. A., Ciccotosto, G. D., Needham, B. E., Fodero, L. R., White, A. R., Masters, C. L., Cappai, R. & Camakaris, J. (2004). J. Neurochem. 91, 423-428.]). The binding of Cu2+ ions to the extracellular copper-binding domain (CuBD) can lower the production of Aβ in cultured cells (Borchardt et al., 1999[Borchardt, T., Camakaris, J., Cappai, R., Masters, C. L., Beyreuther, K. & Multhaup, G. (1999). Biochem. J. 344, 461-467.]). The beneficial effects of Cu2+ binding to the APP have been demonstrated recently in two independent transgenic mouse studies. By supplementing the drinking water with Cu2+, the survival of APP23 mice (carrying a mutant APP that overproduces Aβ) was improved, while there was increased bioavailable Cu2+ and reduced Aβ in the brain (Bayer et al., 2003[Bayer, T. A., Schäfer, S., Simons, A., Kemmling, A., Kamer, T., Tepest, R., Eckert, A., Schüssel, K., Eikenberg, O., Sturchler-Pierrat, C., Abramowski, D., Staufenbiel, M. & Multhaup, G. (2003). Proc. Natl Acad. Sci. USA, 100, 14187-14192.]). Similar effects were achieved by crossing TgCRND8 mice with mice that have raised brain Cu levels owing to the expression of a mutant copper transporter CuATPase7b. This resulted in decreased amyloid plaque and plasma Aβ levels (Phinney et al., 2003[Phinney, A. L., Drisaldi, B., Schmidt, S. D., Lugowski, S., Coronado, V., Liang, Y., Horne, P., Yang, J., Sekoulidis, J., Coomaraswamy, J., Cbishti, M. A., Cox, D. W., Mathews, P. M., Nixon, R. A., Carlson, G. A., St George-Hyslop, P. & Westaway, D. (2003). Proc. Natl Acad. Sci. USA, 100, 14193-14197.]). Structural studies of Cu2+ binding to APP will thus aid the discovery of drugs that mimic the beneficial effects of Cu2+ in and may lead to a treatment for Alzheimer's disease.

The structure of the apo form of the CuBD has been determined using NMR spectroscopy (Barnham et al., 2003[Barnham, K. J., McKinstry, W. J., Multhaup, G., Galatis, D., Morton, C. J., Curtain, C. C., Williamson, N. A., White, A. R., Hinds, M. G., Norton, R. S., Beyreuther, K., Masters, C. L., Parker, M. W. & Cappai, R. (2003). J. Biol. Chem. 278,17401-17407.]). The structure was found to consist of an α-helix packed against a three-strand β-sheet, a fold also observed in several copper chaperones. Copper-binding residues were inferred by titration of Cu2+ ions into a solution of CuBD. The resonance peaks of His147, His151, Tyr168 and Met170 were broadened owing to the paramagnetic interference of Cu2+. A crystallographic study of the CuBD has been pursued to confirm these residues as ligands, to study the binding site in detail and to understand the copper-reduction mechanism.

2. Experimental procedures

2.1. Expression and purification of APP133–189 in Pichia pastoris

The copper-binding domain of APP (residues 133–189) was amplified from APP695 cDNA using the primers CuBDforward, GGTCGACAAAAGAGAGGCTTGCAAATTCTTACACCAGG, and CuBDreverse, GAATTCTTACAGTGGGCAACACACAAACTC. The PCR DNA was cloned as a SalI–EcoRI fragment into XhoI–EcoRI-digested pPIC-9 expression vector (Invitrogen). The pIC9-APP133-189 vector was linearized with BglII and transfected into P. pastoris strain GS115 as previously described (Henry et al., 1997[Henry, A., Masters, C. L., Beyreuther, K. & Cappai, R. (1997). Protein Expr. Purif. 10, 283-291.]). A strongly expressing clone was selected by screening culture supernatants by silver staining of SDS–PAGE gels. Expression cultures were grown for 48 h in YPD medium and induced in YP medium containing 3%(v/v) methanol for 24 h. Cells were removed by centrifugation (10 000g, 277 K, 30 min) and the medium passed through a 0.2 µm filter. The protein was concentrated to 10 ml or less using a stirred-cell concentration device. The concentrated sample was then purified using a Superdex-75 gel-filtration column (Pharmacia Biotech, UK) and eluted with 20 mM MES pH 6.8. The peak corresponding to CuBD, as determined by SDS–PAGE, was concentrated using a Vivaspin-2 (3000 Da molecular-weight cutoff; VivaScience, Germany) to a final concentration of ∼10 mg ml−1. The metal-ion content of the protein was analysed by inductively coupled plasma mass spectrometry (ICP–MS).

2.2. Crystallization

Crystallization trials were carried out at 295 K using the hanging-drop method by mixing 1–2 µl protein solution with an equal volume of the reservoir. The initial crystallization conditions were established using the protein crystallization screen devised by Zeelen et al. (1994[Zeelen, J. P., Hiltunen, J. K., Ceska, T. A. & Wierenga, R. K. (1994). Acta Cryst. D50, 443-447.]) and Crystal Screen II (Hampton Research, USA). After further optimization and streak-seeding with older crystals using cat whiskers, crystals of good diffraction quality could be obtained. Crystal soaking in the presence of Cu2+ is currently being attempted.

2.3. Data collection and processing

The diffraction data from a type A crystal (see §[link]3) were collected at Sector 14-BM-C of the Advanced Photon Source synchrotron (Argonne, Illinois, USA) at 100 K. Data from a type B crystal were collected at 115 K using an in-house MAR Research area detector with Cu Kα X-rays generated by a Rigaku RU-200 rotating-anode X-­ray generator. The crystals were cryoprotected in their respective reservoir buffers supplemented with 12–14%(v/v) glycerol. The data were processed using the HKL suite of programs (Otwinowski, 1993[Otwinowski, Z. (1993). Proceedings of the CCP4 Study Weekend. Data Collection and Processing, edited by L. Sawyer, N. Isaacs & S. Bailey, pp. 56-62. Warrington: Daresbury Laboratory.]) and converted into CCP4 format (Collaborative Computational Project, Number 4, 1994[Collaborative Computational Project, Number 4 (1994). Acta Cryst. D50, 760-763.]). Molecular replacement was attempted using the NMR structure (PDB code 1owt ; Barnham et al., 2003[Barnham, K. J., McKinstry, W. J., Multhaup, G., Galatis, D., Morton, C. J., Curtain, C. C., Williamson, N. A., White, A. R., Hinds, M. G., Norton, R. S., Beyreuther, K., Masters, C. L., Parker, M. W. & Cappai, R. (2003). J. Biol. Chem. 278,17401-17407.]) as a probe model in the CCP4 programs MOLREP (Vagin & Teplyakov, 1997[Vagin, A. & Teplyakov, A. (1997). J. Appl. Cryst. 30, 1022-1025.]) and AMoRe (Navaza, 1994[Navaza, J. (1994). Acta Cryst. A50, 157-163.]).

3. Results and discussion

The domain boundaries of the copper-binding domain (CuBD) were chosen so that the N-terminus (Ser124) followed immediately from the N-terminal growth-factor domain (Rossjohn et al., 1999[Rossjohn, J., Cappai, R., Feil, S. C., Henry, A., McKinstry, W. J., Galatis, D., Hesse, L., Multhaup, G., Beyreuther, K., Masters, C. L. & Parker, M. W. (1999). Nature Struct. Biol. 6, 327-331.]) and the C-terminus (Leu189) fell immediately before the start of a region rich in acidic residues. Initial attempts to crystallize CuBD124–189 resulted in very small needle crystals that could not be optimized despite extensive attempts. We then decided to pursue structure determination using NMR spectroscopy (Barnham et al., 2003[Barnham, K. J., McKinstry, W. J., Multhaup, G., Galatis, D., Morton, C. J., Curtain, C. C., Williamson, N. A., White, A. R., Hinds, M. G., Norton, R. S., Beyreuther, K., Masters, C. L., Parker, M. W. & Cappai, R. (2003). J. Biol. Chem. 278,17401-17407.]). We successfully solved the NMR structure of apo APP124–189, but could not visualize the Cu2+-bound form of CuBD owing to the paramagnetism of Cu2+, which led to severe line-broadening of the spectra. Importantly, the NMR structure revealed a flexible N-­terminal region spanning residues 124–132, which we reasoned might impair crystallization. We therefore expressed another construct in which the flexible N-terminal residues 124–132 were removed. The APP133–189 construct was expressed in P. pastoris, with an expression level of 10–20 mg purified protein per litre. ICP–MS analysis of the purified protein showed insignificant amounts of copper ions.

Two crystallization conditions were discovered from each of the two crystallization screens used. Type A crystals were the first to appear. They were grown in 0.1 M MES pH 5.5, 0.4 M NaCOOH plus 10–15%(w/v) PEG 4000 and usually reached 100–150 µm in each dimension (Fig. 1[link]). They diffracted to a maximal resolution of 1.60 Å with synchrotron radiation (λ = 0.9 Å). The data-collection statistics are given in Table 1[link]. The unit-cell parameters are consistent with the presence of between six and 11 CuBD molecules per asymmetric unit using the Matthews formula (VM = 3.25 and 1.77 Å3 Da−1 for n = 6 and 11, respectively; Matthews, 1968[Matthews, B. W. (1968). J. Mol. Biol. 33, 491-497.]). Calculating the self-rotation function using data between 20 and 4.0 Å resolution revealed complex internal symmetry; the κ = 180° section suggested three twofold axes in 222 symmetry within each asymmetric unit (Fig. 2[link]).

Table 1
Data-collection statistics for crystals of types A and B

Values in parentheses indicate data in the highest resolution shell (1.66–1.60 Å for type A, 1.67–1.61 Å for type B).

Crystal Type A Type B
Maximal resolution (Å) 1.60 1.61
Space group P212121 P212121
Unit-cell parameters    
a (Å) 61.4 31.4
b (Å) 68.0 32.5
c (Å) 127.8 50.2
Redundancy 11.7 (3.4) 2.72 (2.20)
Completeness (%) 88.2 (58.9) 96.2 (89.8)
Completeness >2σ (%) 85.3 (46.9) 86.6 (65.7)
I/σ(I) 25.6 (1.24) 15.5 (5.39)
Rmerge (%) 8.2 (67.1) 5.8 (17.8)
[Figure 1]
Figure 1
Crystals of CuBD grown in (a) 0.1 M MES pH 5.5, 0.4 M NaCOOH plus 10–15%(w/v) PEG 4000 and (b) 0.1 M HEPES pH 8.0 plus 28–32%(w/v) PEG. The longest dimension of a typical crystal grown under both conditions is between 150 and 200 mm.
[Figure 2]
Figure 2
Self-rotation function calculated from diffraction data of type A crystals at κ = 180°, using data between 20.0 and 4.0 Å resolution and the program POLARRFN (Collaborative Computational Project, Number 4, 1994[Collaborative Computational Project, Number 4 (1994). Acta Cryst. D50, 760-763.]). The horizontal and vertical polar coordinates of the rotation axis are ω (0–90° from centre to edge of circle) and φ (plotted around the circumference as shown in the figure). The peaks at φ = 0, 90, 180 and −90° on the circumference arise from crystallographic twofold of the space group.

Type B crystals could be grown in 0.1 M HEPES pH 8.0 plus 28–32%(w/v) PEG 10 000. Crystals had the shape of rectangular prisms and reached 150–200 µm in the longest dimension (Fig. 1[link]b). On an in-house X-ray source, these crystals diffracted strongly to 1.61 Å, the physical limit of our diffractometer setup. The unit-cell parameters (see data-collection statistics in Table 1[link]) are consistent with the presence of one CuBD in the asymmetric unit (VM = 1.94 Å3 Da−1 with n = 1). Molecular-replacement calculations are in progress for both crystal forms. Trials have also been performed to introduce Cu2+ ions into the crystals through soaking. The crystals typically gained a blue–green tint and preliminary diffraction experiments with synchrotron radiation showed anomalous scattering from the Cu2+ ions.

Acknowledgements

The authors thank Irene Volitakis (The Mental Health Research Institute) for the ICP–MS analyses. GKWK is a recipient of the Australian Postgraduate Award from the Australian Government and the Ludo Frevel Scholarship from the International Centre for Diffraction Data. GP and KJB are National Health and Medical Research Council (NHMRC) R. D. Wright Fellows. WJM is an NHMRC Industry Fellow. MWP is an NHMRC Senior Principal Research Fellow. RC is an NHMRC Senior Research Fellow. This work was supported by NHMRC grants to MWP, RC, KJB and CLM and by the Australian Synchrotron Research Program, funded by the Australian Government Major National Research Facilities Program, for access to BioCARS (Sector 14) of the Advanced Photon Source (APS). Use of APS was supported by the US Department of Energy, Basic Energy Sciences, Office of Energy Research. We also thank Harry Tong and other staff at BioCARS for their help with data collection during visits to the APS.

References

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ISSN: 2053-230X
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