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DOI: 10.1038/NCHEM.1299 Protein fold determined by paramagnetic magic-angle spinning solid-state NMR spectroscopy Ishita Sengupta 1, Philippe S. Nadaud 1, Jonathan J. Helmus 1, Charles D. Schwieters 2 and Christopher P. Jaroniec 1 * 1 Department of Chemistry, The Ohio State University, 100 West 18 th Avenue, Columbus, Ohio 43210, USA 2 Division of Computational Bioscience, Center for Information Technology, Building 12A, National Institutes of Health, Bethesda, Maryland 20892, USA *E-mail: jaroniec@chemistry.ohio-state.edu NATURE CHEMISTRY www.nature.com/naturechemistry 1

Figure S1. The pulse scheme used to determine residue-specific longitudinal 15 N relaxation rate constants, R 1, in the GB1 Cys-EDTA-Cu 2+ /Zn 2+ mutants from series of two-dimensional 15 N- 13 CO (2D NCO) correlation spectra recorded with different values of τ relax in the 100 μs to 4 s range. 1 The experiments were performed at 11.7 T (500 MHz 1 H Larmor frequency) and 40 khz MAS rate. Narrow and wide black rectangles correspond to 90 o and 180 o pulses, respectively, and all pulses have phase x unless indicated otherwise. The 1 H, 13 C and 15 N carriers were placed at ~4.7, 175, and 120 ppm, respectively. 1 H- 15 N cross-polarization (CP) 2 was achieved with a ~60 khz 15 N field applied with a tangent ramp, 3 a ~100 khz 1 H field, and a contact time of 1.0 ms. SPECIFIC CP 4 with a ~15 khz 15 N field, a ~25 khz 13 C field with a tangent ramp, and a 7 ms contact time was used to establish the 15 N- 13 CO magnetization transfer. Proton XiX 5 and nitrogen WALTZ-16 6 decoupling was applied at field strengths of ~12 khz and ~3.3 khz, respectively, during periods indicated in the figure. The spin-state-selective excitation (S 3 E) 13 CO- 13 Cα J-decoupling scheme, 7,8 with the delay δ = 2.25 ms, consisted of two separate spectra recorded with selective rsnob 180 o refocusing pulses 9 of 250 μs duration applied to the 13 CO spins at the frequency of 175 ppm (filled black shapes) and 13 Cα spins at the frequency of 55 ppm (filled gray shapes) in either position a or b. The spectra were processed as described by Laage et al. 8 The following phase cycles were employed to record spectra a and b. Spectrum a: φ 1 = 2(x), 2(-x); φ 2 = x, -x; φ 3 = y; ψ = x; receiver = x, -x, -x, x. Spectrum b: φ 1 = 2(x), 2(-x); φ 2 = x, -x; φ 3 = y; ψ = -y; receiver = x, -x, -x, x. Quadrature in the 15 N dimension was achieved by alternating phase φ 2 according to the States method. 10 NATURE CHEMISTRY www.nature.com/naturechemistry 2

Table S1. Summary of longitudinal amide 15 N PRE restraints and repulsive NOE-type distance restraints determined for the six GB1 mutants modified with paramagnetic EDTA-Cu 2+ tags EDTA-Cu 2+ Residue PRE, G N tag position number 1 (s -1 ) a Residue number NOE b 8 4 0.14 ± 0.01 2 * 5 0.26 ± 0.02 17 * 9 0.34 ± 0.05 18 * 14 0.52 ± 0.05 19 * 15 0.54 ± 0.11 20 * 39 0.15 ± 0.01 21 * 40 0.24 ± 0.03 24 * 41 0.14 ± 0.03 25 * 43 0.27 ± 0.02 26 * 44 0.22 ± 0.03 27 * 45 0.14 ± 0.01 28 * 46 0.14 ± 0.01 29 * 47 0.11 ± 0.01 30 * 50 0.11 ± 0.02 31 * 51 0.14 ± 0.01 32 * 52 0.18 ± 0.01 33 * 53 0.29 ± 0.02 34 * 55 0.54 ± 0.11 35 * 56 0.20 ± 0.05 36 * 37 * 38 * 48 * 49 * 19 5 0.19 ± 0.02 7 * 9 0.18 ± 0.01 14 * 10 0.24 ± 0.04 33 * 11 0.19 ± 0.02 34 * 12 0.12 ± 0.02 35 * 15 0.14 ± 0.01 37 * 16 0.21 ± 0.01 43 * 20 0.74 ± 0.09 45 * 21 0.11 ± 0.01 46 * 23 0.19 ± 0.03 53 * 25 0.11 ± 0.02 54 * 26 0.17 ± 0.01 28 0.14 ± 0.01 38 0.12 ± 0.01 39 0.13 ± 0.02 40 0.22 ± 0.03 41 0.18 ± 0.04 42 0.22 ± 0.03 47 0.12 ± 0.01 NATURE CHEMISTRY www.nature.com/naturechemistry 3

Table S1. continued EDTA-Cu 2+ Residue PRE, G N tag position number 1 (s -1 ) a Residue number NOE b 49 0.12 ± 0.01 51 0.15 ± 0.01 55 0.15 ± 0.02 28 21 0.13 ± 0.01 2 * 24 0.33 ± 0.02 4 * 25 0.81 ± 0.05 5 * 26 0.21 ± 0.01 6 * 27 0.21 ± 0.01 7 * 28 0.56 ± 0.07 8 * 29 0.48 ± 0.03 9 * 30 0.22 ± 0.01 10 * 31 0.34 ± 0.03 11 * 32 0.51 ± 0.02 12 * 33 0.18 ± 0.01 13 * 34 0.13 ± 0.01 14 * 35 0.19 ± 0.01 15 * 36 0.12 ± 0.01 17 * 40 0.16 ± 0.01 18 * 41 0.23 ± 0.02 19 * 42 0.14 ± 0.01 20 * 43 0.17 ± 0.01 37 * 38 * 39 * 44 * 45 * 46 * 47 * 48 * 49 * 50 * 51 * 52 * 53 * 54 * 55 * 56 * 42 9 0.20 ± 0.01 7 * 10 0.33 ± 0.09 14 * 11 0.25 ± 0.06 18 * 15 0.12 ± 0.01 19 * 32 0.21 ± 0.03 20 * 33 0.15 ± 0.01 21 * 34 0.24 ± 0.03 24 * NATURE CHEMISTRY www.nature.com/naturechemistry 4

Table S1. continued EDTA-Cu 2+ Residue PRE, G N tag position number 1 (s -1 ) a Residue number NOE b 35 0.33 ± 0.03 25 * 36 0.21 ± 0.01 26 * 37 0.19 ± 0.01 27 * 38 0.38 ± 0.02 29 * 39 0.18 ± 0.02 30 * 43 0.56 ± 0.03 45 * 44 0.15 ± 0.01 47 * 55 0.39 ± 0.02 48 * 56 0.48 ± 0.13 49 * 50 * 51 * 52 * 46 6 0.33 ± 0.03 9 * 7 0.38 ± 0.03 10 * 8 0.15 ± 0.03 11 * 17 0.17 ± 0.02 13 * 19 0.13 ± 0.03 14 * 21 0.12 ± 0.01 15 * 23 0.18 ± 0.02 18 * 24 0.16 ± 0.01 29 * 25 0.12 ± 0.02 30 * 32 0.11 ± 0.02 31 * 33 0.11 ± 0.02 40 * 34 0.12 ± 0.03 42 * 35 0.15 ± 0.03 55 * 36 0.14 ± 0.03 37 0.12 ± 0.02 38 0.13 ± 0.03 39 0.12 ± 0.02 41 0.25 ± 0.02 43 0.11 ± 0.02 44 0.21 ± 0.03 45 0.36 ± 0.02 51 1.11 ± 0.15 52 0.37 ± 0.04 56 0.13 ± 0.01 53 2 0.15 ± 0.02 9 * 5 0.15 ± 0.01 10 * 6 0.13 ± 0.02 11 * 7 0.18 ± 0.05 13 * 12 0.14 ± 0.03 16 * 14 0.14 ± 0.03 17 * 15 0.15 ± 0.03 19 * NATURE CHEMISTRY www.nature.com/naturechemistry 5

Table S1. continued EDTA-Cu 2+ Residue PRE, G N tag position number 1 (s -1 ) a Residue number NOE b 21 0.12 ± 0.01 24 * 43 0.12 ± 0.01 25 * 49 0.17 ± 0.04 27 * 51 0.21 ± 0.03 29 * 31 * 32 * 33 * 34 * 36 * 37 * 38 * 39 * 41 * 42 * 46 * a PREs were calculated as Γ N 1 = R 1 (Cu 2+ ) R 1 (Zn 2+ ), where 15 N R 1 values for the corresponding pair of EDTA-Cu 2+ and EDTA-Zn 2+ tagged proteins were obtained by fitting residue-specific relaxation trajectories to decaying single exponentials. A total of 110 quantitative PRE restraints (77 for residues located in regular secondary structure elements and 33 for loop residues) were determined for the six GB1 analogs and used in the structure calculations via the PREPot potential term (see main text and Supplementary Table S3 for additional details). b For residues where the PRE measurements yielded values of Γ N 1 0.10 s -1 (indicated by asterisks) the PRE restraints were converted into purely repulsive NOE-type distance restraints with a lower-bound cutoff of 15.1 Å and used in the structure calculations via the NOEPot potential term. A total of 121 residues for the six GB1 analogs fell into this category (89 located in regular secondary structure elements and 32 loop residues). NATURE CHEMISTRY www.nature.com/naturechemistry 6

Table S2. TALOS+ dihedral angle restraints for GB1 a Residue number (degrees) (degrees) 2-115 ± 36 140 ± 36 3-129 ± 26 149 ± 22 4-133 ± 22 132 ± 20 5-110 ± 24 122 ± 20 6-105 ± 30 117 ± 30 7-101 ± 30 124 ± 30 8-108 ± 54 135 ± 54 9-109 ± 70 170 ± 40 10-67 ± 30-32 ± 22 11-102 ± 34-4 ± 32 12-117 ± 62 128 ± 42 13-125 ± 28 161 ± 28 14-150 ± 62 161 ± 34 15-135 ± 34 151 ± 26 16-121 ± 34 151 ± 32 17-132 ± 20 156 ± 20 18-128 ± 40 138 ± 26 19-121 ± 20 129 ± 22 20-114 ± 54 163 ± 30 21-84 ± 36-18 ± 32 22 23-62 ± 20-37 ± 20 24-63 ± 20-40 ± 20 25-68 ± 20-38 ± 20 26-63 ± 20-42 ± 20 27-63 ± 20-40 ± 24 28-61 ± 20-41 ± 20 29-64 ± 20-46 ± 20 30-67 ± 20-37 ± 20 31-65 ± 20-42 ± 20 32-67 ± 20-41 ± 20 33-64 ± 20-44 ± 20 34-63 ± 20-44 ± 20 35-60 ± 20-43 ± 20 36-61 ± 20-27 ± 20 37-97 ± 26 7 ± 20 38 86 ± 20 13 ± 20 39-84 ± 32 134 ± 20 40-115 ± 48 138 ± 44 41 42-113 ± 32 128 ± 36 43-111 ± 38 151 ± 28 44-129 ± 44 158 ± 22 45-145 ± 32 134 ± 34 NATURE CHEMISTRY www.nature.com/naturechemistry 7

Table S2. continued Residue number (degrees) (degrees) 46-112 ± 32 133 ± 32 47 48-74 ± 22-25 ± 38 49-104 ± 20 6 ± 34 50 61 ± 22 34 ± 32 51-102 ± 48 133 ± 20 52-116 ± 26 153 ± 32 53-129 ± 30 147 ± 20 54-129 ± 26 132 ± 20 55-107 ± 42 127 ± 28 a Dihedral restraints were obtained using the 13 C and 15 N solid-state NMR chemical shifts reported for microcrystalline GB1 (BMRB entry 15156) and the TALOS+ program 11 in the no-proton mode (http://spin.niddk.nih.gov/bax/nmrserver/talos/). For predicted dihedral angles having uncertainties of less than ±20 o, the uncertainties were set to ±20 o for the structure calculations. NATURE CHEMISTRY www.nature.com/naturechemistry 8

Table S3. Potential term parameters during structure calculations Force constant schedule a Potential name Description Initial minimization (force constant units) Simulated annealing and dynamics PrePot SSNMR PRE restraints 0.05 ramped: 0.05 Æ 1.0 (kcal sec/mol) NOEPot repulsive distance (kcal/mol/å 2 2 ramped: 2 Æ 30 ) restraints CDIH TALOS+ based dihedral (kcal/mol/rad 2 1000 1000 ) restraints COLL radius of gyration (kcal/mol/å 2 1000 1000 ) restraint RAMA knowledge-based 1 1 (kcal/mol) dihedral restraints HBDB knowledge-based 2/1 2/1 (kcal/mol) hydrogen bond restraints ResidueAffPot knowledge-based 50/1 50/1 (kcal/mol/å) contact potential BOND (kcal/mol/å 2 bond length 1000 1000 ) ANGL (kcal/mol/rad 2 bond angle 200 ramped: 200 Æ 500 ) IMPR (kcal/mol/rad 2 improper dihedral angle 50 ramped: 50 Æ 5000 ) DIHE (kcal/mol/rad 2 ) b dihedral angle 50 ramped: 50 Æ 5000 VDW quartic atom-atom 0.004 ramped: 0.004 Æ 4 (kcal/mol/å 4 ) c repulsion Cα-only all atoms Entries with two slash-separated values correspond to the anneal value and refine value, respectively. Only applied to the EDTA-Cu 2+ sidechain dihedral angles for which the RAMA term contains no information. In addition atomic radii are scaled by a value of 1.2 during initial dynamics and minimization and scaled by a value ramped from 0.9 to 0.78 during simulated annealing. NATURE CHEMISTRY www.nature.com/naturechemistry 9

References 1. Nadaud, P. S., Helmus, J. J., Sengupta, I. & Jaroniec, C. P. Rapid acquisition of multidimensional solid-state NMR spectra of proteins facilitated by covalently bound paramagnetic tags. J. Am. Chem. Soc. 132, 9561-9563 (2010). 2. Pines, A., Gibby, M. G. & Waugh, J. S. Proton-enhanced NMR of dilute spins in solids. J. Chem. Phys. 59, 569-590 (1973). 3. Hediger, S., Meier, B. H. & Ernst, R. R. Adiabatic passage Hartmann-Hahn crosspolarization in NMR under magic-angle sample spinning. Chem. Phys. Lett. 240, 449-456 (1995). 4. Baldus, M., Petkova, A. T., Herzfeld, J. & Griffin, R. G. Cross polarization in the tilted frame: assignment and spectral simplification in heteronuclear spin systems. Mol. Phys. 95, 1197-1207 (1998). 5. Detken, A., Hardy, E. H., Ernst, M. & Meier, B. H. Simple and efficient decoupling in magic-angle spinning solid-state NMR: the XiX scheme. Chem. Phys. Lett. 356, 298-304 (2002). 6. Shaka, A. J., Keeler, J. & Freeman, R. Evaluation of a new broadband decoupling sequence: WALTZ-16. J. Magn. Reson. 53, 313-340 (1983). 7. Meissner, A., Duus, J. O. & Sorensen, O. W. Spin-state-selective excitation. Application for E.COSY-type measurement of J(HH) coupling constants. J. Magn. Reson. 128, 92-97 (1997). 8. Laage, S. et al. Transverse-dephasing optimized homonuclear J-decoupling in solid-state NMR spectroscopy of uniformly 13 C-labeled proteins. J. Am. Chem. Soc. 131, 10816-10817 (2009). 9. Kupce, E., Boyd, J. & Campbell, I. D. Short selective pulses for biochemical applications. J. Magn. Reson. B 106, 300-303 (1995). 10. States, D. J., Haberkorn, R. A. & Ruben, D. J. A two-dimensional nuclear Overhauser experiment with pure absorption phase in four quadrants. J. Magn. Reson. 48, 286-292 (1982). 11. Shen, Y., Delaglio, F., Cornilescu, G. & Bax, A. TALOS+: A hybrid method for predicting protein backbone torsion angles from NMR chemical shifts. J. Biomol. NMR 44, 213-223 (2009). NATURE CHEMISTRY www.nature.com/naturechemistry 10