The Fic protein Doc uses an inverted substrate to phosphorylate and. inactivate EF-Tu

Similar documents
Chapter 6. The interaction of Src SH2 with the focal adhesion kinase catalytic domain studied by NMR

Nature Structural & Molecular Biology: doi: /nsmb Supplementary Figure 1

Table S1. Overview of used PDZK1 constructs and their binding affinities to peptides. Related to figure 1.

Supplementary Information. Overlap between folding and functional energy landscapes for. adenylate kinase conformational change

Supplemental Information. Structural and Mechanistic Paradigm. of Leptin Receptor Activation Revealed

Supplemental data for

Supplementary figure 1 Application of tmfret in LeuT. (a) To assess the feasibility of using tmfret for distance-dependent measurements in LeuT, a

Structural characterization of NiV N 0 P in solution and in crystal.

Supplementary Information. The protease GtgE from Salmonella exclusively targets. inactive Rab GTPases

Nature Structural and Molecular Biology: doi: /nsmb Supplementary Figure 1. Definition and assessment of ciap1 constructs.

Supplementary Figure 1. Biochemical and sequence alignment analyses the

Supplementary Information

Nature Structural & Molecular Biology: doi: /nsmb Supplementary Figure 1

Supplementary Materials for

SOCS3 binds specific receptor JAK complexes to control cytokine signaling by direct kinase inhibition SUPPLEMENTARY INFORMATION

SUPPLEMENTARY INFORMATION

Supplementary Figure 1 Crystal contacts in COP apo structure (PDB code 3S0R)

The Aβ40 and Aβ42 peptides self-assemble into separate homomolecular fibrils in binary mixtures but cross-react during primary nucleation

Sensitive NMR Approach for Determining the Binding Mode of Tightly Binding Ligand Molecules to Protein Targets

Supporting Information

Supplementary figure 1. Comparison of unbound ogm-csf and ogm-csf as captured in the GIF:GM-CSF complex. Alignment of two copies of unbound ovine

Supplementary Figures

SUPPLEMENTARY INFORMATION

Serine-7 but not serine-5 phosphorylation primes RNA polymerase II CTD for P-TEFb recognition

Supplementary Information. Structural basis for precursor protein-directed ribosomal peptide macrocyclization

Supplementary Information for

Supplementary Information for. Direct nitration and azidation of aliphatic carbons by an iron-dependent halogenase

THE CRYSTAL STRUCTURE OF THE SGT1-SKP1 COMPLEX: THE LINK BETWEEN

Supplemental Information

SUPPLEMENTARY INFORMATION

Analysis of nucleotide binding to p97 reveals the properties of a tandem AAA hexameric ATPase

Purification, SDS-PAGE and cryo-em characterization of the MCM hexamer and Cdt1 MCM heptamer samples.

SUPPLEMENTARY INFORMATION

Impact of the crystallization condition on importin-β conformation

Supplemental Information. Molecular Basis of Spectral Diversity. in Near-Infrared Phytochrome-Based. Fluorescent Proteins

Supplemental Information. The Mitochondrial Fission Receptor MiD51. Requires ADP as a Cofactor

National de la Recherche Scientifique and Université Paris Descartes, Paris, France.

Supporting Information

Supplementary Materials: Localization and Spectroscopic Analysis of the Cu(I) Binding Site in Wheat Metallothionein Ec-1

SUPPLEMENTARY INFORMATION

Supplementary Information. The Solution Structural Ensembles of RNA Kink-turn Motifs and Their Protein Complexes

Interpreting and evaluating biological NMR in the literature. Worksheet 1

Structural basis for catalytically restrictive dynamics of a high-energy enzyme state

Supporting information for

SUPPLEMENTARY INFORMATION

Supplementary Information to

Bacterial protease uses distinct thermodynamic signatures for substrate recognition

SUPPLEMENTARY INFORMATION

for Molecular Biology and Neuroscience and Institute of Medical Microbiology, Rikshospitalet-Radiumhospitalet

Table S1. Primers used for the constructions of recombinant GAL1 and λ5 mutants. GAL1-E74A ccgagcagcgggcggctgtctttcc ggaaagacagccgcccgctgctcgg

Supplementary material

pyridoxal phosphate synthase

ml. ph 7.5 ph 6.5 ph 5.5 ph 4.5. β 2 AR-Gs complex + GDP β 2 AR-Gs complex + GTPγS

Nature Structural & Molecular Biology: doi: /nsmb.3194

SUPPLEMENTARY INFORMATION

SUPPLEMENTARY ONLINE DATA

Structural basis of PROTAC cooperative recognition for selective protein degradation

Supplementary Information

Protein Dynamics. The space-filling structures of myoglobin and hemoglobin show that there are no pathways for O 2 to reach the heme iron.

NMR in Medicine and Biology

In Situ Gelation-Induced Death of Cancer Cells Based on Proteinosomes

SUPPLEMENTARY INFORMATION

SUPPLEMENTARY FIGURES

Dr. Yonca Yuzugullu PERG (Protein Engineering Research Group)

Tridip Sheet, Raja Banerjee*

Protein Structure Determination using NMR Spectroscopy. Cesar Trinidad

Supporting Information. Labeled Ligand Displacement: Extending NMR-based Screening of Protein Targets

17. Biomolecular Interaction

Supplementary Information. Synthesis and biological activity of a CXCR4-targeting bis(cyclam) lipid

SUPPLEMENTARY INFORMATION

Figure S1. Interaction of PcTS with αsyn. (a) 1 H- 15 N HSQC NMR spectra of 100 µm αsyn in the absence (0:1, black) and increasing equivalent

Introduction to" Protein Structure

Supporting Information

Cryo-EM data collection, refinement and validation statistics

Supporting Information for. Jesinghaus, Rachael Barry, Zemer Gitai, Justin Kollman and Enoch P. Baldwin

Supplementary Materials for

Supplemental Data SUPPLEMENTAL FIGURES

Nature Structural and Molecular Biology: doi: /nsmb.2938

SUPPLEMENTARY INFORMATION

Nature Structural & Molecular Biology: doi: /nsmb Supplementary Figure 1

Supplementary Materials for

SUPPLEMENTARY FIGURES. Figure S1

Supplementary materials. Crystal structure of the carboxyltransferase domain. of acetyl coenzyme A carboxylase. Department of Biological Sciences

Supporting Information

Simulative and experimental characterization of a ph-dependent

SUPPLEMENTARY INFORMATION

Sample preparation and characterization around SAXS

Acta Crystallographica Section D

Structure of the α-helix

According to the manufacture s direction (Pierce), RNA and DNA

Enhancing hydrogen production of microalgae by redirecting electrons from photosystem I to hydrogenase

Deconvoluting the responses of polymer-scaffolded dynamic combinatorial libraries to biomacromolecular templates

Supplementary Figure 1: Power dependence of hot-electrons reduction of 4-NTP to 4-ATP. a) SERS spectra of the hot-electron reduction reaction using

Supporting Information

Supporting Protocol This protocol describes the construction and the force-field parameters of the non-standard residue for the Ag + -site using CNS

SUPPLEMENTARY INFORMATION

Targeting protein-protein interactions: A hot topic in drug discovery

SUPPLEMENTARY INFORMATION

James B. Munro, Roger B. Altman, Nathan O Connor, and Scott C. Blanchard

type GroEL-GroES complex. Crystals were grown in buffer D (100 mm HEPES, ph 7.5,

Transcription:

The Fic protein Doc uses an inverted substrate to phosphorylate and inactivate EF-Tu Daniel Castro-Roa 1, Abel Garcia-Pino 2,3 *, Steven De Gieter 2,3, Nico A.J. van Nuland 2,3, Remy Loris 2,3, Nikolay Zenkin 1 *. 1 Centre for Bacterial Cell Biology, Institute for Cell and Molecular Biosciences, Newcastle University, Baddiley-Clark Building, Richardson Road, Newcastle upon Tyne, NE2 4AX, UK; 2 Structural Biology Brussels, Department of Biotechnology (DBIT), Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels, Belgium; 3 Molecular Recognition Unit, Department of Structural Biology, VIB, Pleinlaan 2, B-1050 Brussels, Belgium D.C-R and A.G-P contributed equally to this work and should be considered co-first authors. *Correspondence to: Nikolay Zenkin, PhD Centre for Bacterial Cell Biology Institute for Cell and Molecular Biosciences Newcastle University Baddiley-Clark Building Richardson Road Newcastle upon Tyne NE2 4AX, UK Phone: +44(0)1912083227 FAX: +44(0)1912083205 E-mail: n.zenkin@ncl.ac.uk Abel Garcia-Pino, PhD Structural Biology Brussels Department of Biotechnology Vrije Universiteit Brussel Building E, Pleinlaan 2 Brussels B-1050, Belgium Phone: +32 (0)2 6291025 FAX: +32 (0)2 6291963 E-mail: agarciap@vub.ac.be 1

Supplementary Results. Supplementary Figure 1. Images of full gels, TLCs and TLEs produced in this work. Note that some gels were cut at the bottom before phosphorimaging to reduce the signal of radiolabeled NTPs migrating at the bottom of the gel. 2

Supplementary Figure 2. Kinetics of EF-Tu phosphorylation in the presence of ATP or GTP. Data are mean of three independent experiments and error bars are standard deviations. Data were fitted into a single-exponential equation and normalized to the predicted maximum, which was taken as 100. ± sign represents standard error of the fit. 3

4

Supplementary Figure 3. Interplay between EF-Tu, Doc and nucleotides: representative ITC titrations. Titration of EF-Tu into Doc in 1mM GDP (a), EF-Tu (free state) into Doc (b), and EF-Tu into Doc in 1 mm of GMPPNP (c). (d) EF-Tu binding to Doc monitored by the changes in intensity ratio (I/I o ) of the 1 H/ 15 N HSQC spectrum of Doc. Residues S27, R38, R64, L77 as function of EF-Tu concentration were used as probe. (e) AMPPNP binding to Doc followed by chemical shift perturbations (Δδ) as function of AMPPNP concentration of the 1 H/ 15 N HSQC spectrum of Doc. Residues Y20, F68, N78 were used as probe. Titration of non-hydrolysable nucleotides into the pre-formed Doc:EF-Tu:GDP complex AMPPNP (f), GMPPNP (g), and UMPPNP (h). Titration of Doc mutants with EF-Tu in 1 mm GDP, Doc N78W (i), Doc H66Y (j), Doc R64G (k), and Doc with the EF-Tu T382V mutant (l). Titration of AMPPNP into the Doc N78W :EF-Tu:GDP complex (m). Titration of Doc with EF-Tu in the NMR conditions (n). Titrations in the presence of Phd 52-73 (the antitoxin domain of Phd) and 1 mm GDP, EF-Tu into Doc (o) and AMPPNP into the preformed Doc:EF-Tu complex (p). See Supplementary Table 1 and Online Methods for further details. 5

6

Supplementary Figure 4. LC-MS/MS analysis of peptides from EF-Tu and EF-Tu treated with Doc and ATP. The analysis of the LC-MS/MS spectra (the EF-Tu spectra in (a) and the spectra of the Doc-treated EF-Tu in (b)) shows that the peptide consisting of the region 374 FAIREGGRTVGAGVVAK 390 has a mass of 1688.9674 Da (m/z ratio 844.4837) in the non-treated EF-Tu, and a mass of 1768.9312 Da (m/z ratio 884.4656) in the Doc-treated EF-Tu. The difference in mass between both peptides equals 79.9638 Da, which is almost identical to the average increase in mass expected from the introduction of a phosphate group (79.9799 Da). Bottom part of each panel is magnification of the upper part. Other clusters of peaks are other peptides. Peaks in clusters are natural isotopes of the same peptide. 7

Supplementary Figure 5. Characterization of the EF-Tu and Doc mutants by CD spectroscopy. (a) The Figure shows that the EF-Tu T382V mutant has a nearly identical far UV CD spectrum as the wild type protein (Figure inset, EF-Tu T382V in red and EF-Tu in blue) and both proteins unfold approximately at the same temperature (EF-Tu T382V at 52.6 C and EF- Tu at 53.2 C), which suggests that this surface mutation has a negligible effect on the overall structure and stability of the protein. (b) The R64G (in blue) and H66Y (in red) surface mutations do not affect the overall secondary structure of Doc (in black) as monitored by far UV CD. All CD measurements were done on a Jasco 715 spectropolarimeter, in Tris-HCl ph 7.4, 40 mm NH 4 Cl, 10 mm MgCl 2, 1 mm TCEP. 8

Supplementary Figure 6. Dephosphorylation of EF-Tu by Doc in the presence of GDP. The scheme of the experiment is shown above the radiogram (see also Fig. 3). EF-Tu 32 P- phosphorylated by Doc for 30 min to ensure full usage of γ[ 32 P]-ATP was then incubated with or without 5 µm Phd and/or 1 mm GDP for 2 hours and products analyzed by TLC. For GDP mobility standard α[ 32 P]-GTP was used in the reaction of EF-Tu phosphorylation, which resulted in formation of α[ 32 P]-GDP. Nonradioactive standards, visualized under UV254 are marked with radioactive spots before phosphorimaging. Not all EF-Tu can be dephosphorylated even after prolonged incubation due to either aggregation or to competition from phosphorylation. The identity of the of EF-Tu spot at the start of chromatogram is verified by addition of Ni 2+ -NTA-agarose beads that sequester the His-tagged EF-Tu before spotting on TLC plate 9

10

Supplementary Figure 7. Assignment of Doc and NMR chemical shift perturbations. (a) 1 H- 15 N HSQC spectrum of Doc and cross peak assignment (b) Chemical shift perturbations observed in the 1 H- 15 N HSQC spectrum of Doc upon addition of 0 μm, 34.0 μm, 58.0 μm 123.3 μm, 197.3 μm of EF-Tu. (c) Chemical shift perturbations observed in the 1 H- 15 N HSQC spectrum of Doc upon addition of 0 mm, 1.4 mm, 2.7 mm 9.0 mm, 15.0 mm, 25.8 mm and 40 mm of AMPPNP. (d) Mapping on the surface of Doc of the observed chemical shifts perturbations (in red) used for the docking of AMPPNP on Doc. Residues R19, Y20, G22, L23, G25, F68, R74, N78, D99, T101 and V102 are shown in red (see Figure 5 and Supplementary Table 3 for further details). 11

Supplementary Figure 8. Determination of experimental SAXS parameters. Guinier analysis of the experimental SAXS curves (in red) and the theoretical curves (in black) derived from the models, for Doc (a), EF-Tu:GDP (b) and Doc:EF-Tu:GDP (c). In every case the curves corresponding to the experimental data are displayed up by one logarithmic unit for clarity. (d) P(r) functions obtained from the scattering curves using GNOM 21 for Doc (in black), EF-Tu:GDP (in blue) and Doc:EF-Tu:GDP (in red). (e) Stereo view of Doc:EF- Tu:GDP representative solutions that fit to the experimental data with χ 2 between 0.9 and 1.1. In the Figure Doc is represented as ribbons and EF-Tu as a blue surface. The solutions superimpose with a core r.m.s.d below 1.5 Å over 510 Cα atoms. Plots of r.m.s.d. versus χ 2 12

(f) and χ 2 versus model number (g). Selected solutions were clustered into three groups (blue, green and orange circles). Blue lines demark the χ 2 range of the final solutions. 13

Supplementary Figure 9. Chemical shift based model of Doc bound to ATP. The ATP bound to Doc in the complex is shown as purple sticks. The orientation of the nucleotide in the active site is antiparallel to that observed in FIC-like proteins (shown in green, based on the structure of NmFic in complex with AMPPNP, pdbid 3S6A 1 ), presenting the γ-phosphate moiety toward H66 and the site where EF-Tu binds. Doc is colored in light grey and active site residues H66, K73 and R74 are shown as black lines. In typical Fic domains K73 is replaced by a glycine, which removes the steric hindrance and allows nucleotide binding, and constitutes a major difference in the active site motif between both subfamilies. 14

Supplementary Figure 10. Phd binding site overlaps the NTP binding site on Doc. When bound to Doc, the C-terminal domain of Phd (in yellow, based on the coordinates of the Doc:Phd complex, pdbid 3K33 24 ) occupies the NTP site (represented by the bound ATP molecule in purple). Note that the site where the NTP binds in Fic-like domains (in green) remains free in the Doc-Phd complex. 15

Supplementary Table 1. Interplay between Doc, EF-Tu and nucleotides. The binding affinities were determined from fitting a single interaction model to the experimental data from ITC and NMR titrations. Data represent mean values ± s.d. See Supplementary Figure 3 for representative titrations. Experiment Technique Kd Number of experiments EF-Tu titrated into Doc ITC 8 ± 4 μm 3 EF-Tu titrated into Doc in phosphate ITC 6 ± 1 μm 3 EF-Tu titrated into Doc in phosphate NMR 16.3 μm 1 EF-Tu titrated into Doc in 1mM GDP ITC 1.7 ± 0.7 μm 3 EF-Tu titrated into Doc in 1mM GMPPNP ITC 50 ± 7 μm 3 EF-Tu titrated into Doc H66Y in 1mM GDP ITC 4 ± 2 μm 3 EF-Tu T382V titrated into Doc in 1mM GDP ITC 10 ± 7 μm 3 EF-Tu titrated into Doc R64G in 1mM GDP ITC no binding 2 EF-Tu titrated into Doc in 1mM GDP in Phd 52-73 ITC no binding 2 EF-Tu titrated into Doc N78W in 1mM GDP ITC 3 ± 1 μm 3 AMPPNP titrated into Doc NMR 7.2 mm 1 AMPPNP titrated into (preformed Doc:EF-Tu:GDP) ITC 0.26 ± 0.05 μm 3 GMPPNP titrated into (preformed Doc:EF-Tu:GDP) ITC 4.4 ± 0.4 μm 3 UMPPNP titrated into (preformed Doc:EF-Tu:GDP) ITC no binding 2 AMPPNP titrated into (preformed Doc N78W :EF-Tu:GDP) ITC 45 ± 1 μm 3 AMPPNP titrated into Doc:EF-Tu:GDP and Phd 52-73 ITC no binding 2 Supplementary Table 2. SAXS parameters. Theoretical and experimental molecular weights of Doc, EF-Tu, and the Doc:EF-Tu as obtained from the SAXS curves. Using an R SAS cutoff of 0.005 and Chi-values of 1.5 or lower, model-data agreements can be reliably identified (Rambo & Tainer, Nature 2013) Specie Experimental Molecular Weight SAXS (kda) Experimental Molecular Weight MALS (kda) Theoretical Molecular Weight (kda) Rg (Å) (exps/model) Dmax(Å) χ 2 R SAS 16

Doc 15.0 14.3 14.7 16.7/16.3 56.4 0.8 0.0027 EF-Tu 44.1 43.9 43.7 23.6/23.8 77.7 1.1 0.0021 0.0029 Doc:EF-Tu:GDP 56.0 56.7 57.0 25.8/24.6 74.3 0.9 Additional SAXS parameters: Specie Vc (model ) Vc (exp) V SAS Rg (model) Rg (exp) Io (model) Io (exp) Doc 166.86 174.93 0.00213 16.3 16.7 595.18 632.69 EF-Tu 390.0 373.2 0.00203 23.8 23.6 861.32 833.1 121.84 Doc:EF-Tu:GDP 409.7 421.4 0.00077 24.6 25.8 118.5 Supplementary Table 3. Chemical shift perturbations used for docking. Residues with chemical shift perturbations above 2σ selected for the docking experiments. Residue Experiment S27 R64 H66 R19 Y20 G22 L23 G25 F68 R74 N78 D99 Docking of EF-Tu to Doc Docking of EF-Tu to Doc Docking of EF-Tu to Doc 17

T101 V102 18