Abstract
The deuteration of proteins and selective labeling of side chain methyl groups has greatly enhanced the molecular weight range of proteins and protein complexes which can be studied using solution NMR spectroscopy. Protocols for the selective labeling of all six methyl group containing amino acids individually are available, however to date, only a maximum of five amino acids have been labeled simultaneously. Here, we describe a new methodology for the simultaneous, selective labeling of all six methyl containing amino acids using the 115 kDa homohexameric enzyme CoaD from E. coli as a model system. The utility of the labeling protocol is demonstrated by efficiently and unambiguously assigning all methyl groups in the enzymatic active site using a single 4D 13C-resolved HMQC–NOESY–HMQC experiment, in conjunction with a crystal structure. Furthermore, the six fold labeled protein was employed to characterize the interaction between the substrate analogue (R)-pantetheine and CoaD by chemical shift perturbations, demonstrating the benefit of the increased probe density.
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Introduction
Since the mid-1990s, NMR methodologies have been developed to enable the study of larger proteins and complexes up to 1 MDa in size (Gardner and Kay 1997; Sprangers and Kay 2007). Improvements in technology and methodology have come in the forms of improved hardware (i.e. higher field NMR spectrometers along with cryogenic probes), optimized NMR experiments (i.e. TROSY) (Yamazaki et al. 1994; Pervushin et al. 1997; Tugarinov et al. 2003) as well as the development of labeling strategies to perdeuterate proteins and to re-introduce NMR-active nuclei in methyl groups at specific locations on the amino acid side chain (Goto and Kay 2000; Tugarinov et al. 2004; Religa and Kay 2010; Kerfah et al. 2015c). Gardner, Goto and Kay pioneered the selective labeling of amino acids in the 1990’s when they published work detailing how to selectively label the δ1-methyl position of isoleucine and the δ-methyl positions of leucine as well as the γ-methyl positions of valine by supplementing the growth medium with [3,3-2H2] 13C 2-ketobutyrate and [3-2H] α-ketoisovalerate, respectively (Gardner and Kay 1997; Goto et al. 1999). Since then, labeling schemes have been expanded to the extent that all six methyl containing amino acids can be individually labeled in separate samples either through the use of labeled amino acid precursors (I, L, V) (Gardner and Kay 1997; Goto et al. 1999; Hajduk et al. 2000; Gross et al. 2003), or by supplementing the growth medium directly with selectively labeled amino acids (M, A, T) (Isaacson et al. 2007; Fischer et al. 2007; Gelis et al. 2007; Ayala et al. 2009; Stoffregen et al. 2012; Velyvis et al. 2012). In addition to being able to selectively label individual residues, protocols have been developed for the simultaneous labeling of multiple amino acids including ILV, MILV, ILVA or MILVT (Gross et al. 2003; Tugarinov and Kay 2003b; Lichtenecker et al. 2004; Gelis et al. 2007; Velyvis et al. 2009; Godoy-Ruiz et al. 2010; Saio et al. 2014). However, to the authors’ knowledge, to date no protocol has been published where all six methyl containing amino acids have been labeled simultaneously.
In order to ensure that detailed structural and functional information can be obtained from NMR experiments, resonance assignment is required. The use of point mutations to assign methyl groups in selectively labeled proteins has been well described and has become common practice (Sprangers and Kay 2007; Velyvis et al. 2009; Religa et al. 2010). However, this process can be fairly labor and resource intensive and mutations frequently result in significantly reduced or limited protein expression. In cases where high protein expression is obtained, replacement of a methyl group bearing amino acid with a similar residue (Crublet et al. 2014) can lead to dramatic changes in the chemical shifts of amino acids in spatial proximity to the mutation site, making unambiguous identification of the missing methyl peak challenging (Xu and Matthews 2013a). Due to these difficulties, a number of additional methods have been developed for the assignment of methyl groups, including the implementation of new pulse programs which correlate the methyl group of certain amino acids to the backbone via the aliphatic side chain (Tugarinov and Kay 2003a, b; Kerfah et al. 2015a), or alternatively the use of high dimensional methyl–methyl NOESY spectra to utilize methyl–methyl networks (Tugarinov et al. 2005; Sounier et al. 2007). Automated programs such as MAP-XS or FLAMEnGO utilize a pre-existing crystal structure of the protein to facilitate peak assignment based on predicted chemical shifts or an expected methyl–methyl NOESY cross peak network (Xu et al. 2009; Xu and Matthews 2013b; Chao et al. 2014). Although these programs are able to produce accurate assignments, the ambiguity present in the multidimensional NOESY datasets acquired with either ILV or ILVA labeled protein requires the programs to be supplemented with additional experimental information, including PRE data, data from through bond experiments or assignments derived from point mutations, in order to provide a more complete resonance assignment or to assign resonances with a higher degree of confidence. To address these limitations, the work described in this manuscript demonstrates the simultaneous, selective incorporation of isotope labels at all methyl positions (except the Ile Cγ position) of the six methyl containing amino acids (MILVAT). By extending the labeling strategy to include all six amino acids, we were able to use a single 4D 13C-resolved HMQC–NOESY–HMQC experiment recorded on a single NMR sample to unambiguously assign all methyl groups in and around the enzymatic pocket of CoaD.
Materials and methods
Growth and expression of CoaD
Escherichia coli BL21(DE3) chemically competent cells (NEB product # C2530H) were transformed with 67 ng of pTrcHis2 B plasmid (Thermo Fisher Scientific) encoding the full length E. coli phosphopantetheine adenylyltransferase (PPAT) CoaD (Uniprot ID: P0A6I6) enzyme followed by an uncleavable, C-terminal His6 tag. 5 mL nutrient rich LB medium containing carbenicillin (100 μg/mL) was inoculated with a single colony and grown until an optical density at 600 nm (OD600) of 0.6 was achieved. At this point, 1 mL of LB culture was used to inoculate 50 mL of fully protonated M9 minimal medium, which was grown overnight at 37 °C with agitation. In all M9 growths, 1 g/L of 15N-amonium chloride and 4 g/L of protonated 12C-glucose were used as the principal nitrogen and carbon sources, respectively. E. coli cells were acclimated to growth in D2O by growing the cells in 50 mL of M9 medium containing increasing concentrations of D2O (30, 70 and 100 %) over a period of three days. On each occasion, 5 mL of the previous starter culture was used to inoculate the new growth which was left to grow at 37 °C overnight with agitation.
The 100 % D2O overnight starter culture was used to inoculate 1 L of 100 % D2O M9 medium to a starting OD600 of 0.1. E. coli cells were grown at 37 °C with agitation until an OD600 of 0.7 was achieved. At this stage, the temperature of the incubator was reduced to 18 °C and the desired combination of selectively labeled precursors and amino acids (Table 1), resuspended in 100 % D2O, was added to the growth medium and left for 1 h. Following the 1 h incubation period, expression of CoaD was induced using 250 μM isopropyl β-d-1-thiogalactopyranoside (IPTG) and cells were left growing at 18 °C for 18 h. Cells were harvested by centrifugation, washed with 1 × phosphate buffered saline (PBS) buffer and stored at −20 °C.
Purification of CoaD
Escherichia coli cells containing the overexpressed CoaD were resuspended in binding buffer (10 mL/g of cell pellet; 20 mM Tris pH 8.0, 500 mM sodium chloride, 1 mM tris(2-carboxyethyl)phosphine (TCEP), 20 mM imidazole), containing Roche Protease Inhibitor without ethylenediamine-tetraacetic acid (EDTA) and sonicated. Cell lysate was centrifuged at 40,000g for 30 min to remove insoluble cell debris, and the soluble lysate was passed through a 0.2 μm filter before being mixed with 5 mL Ni Sepharose 6 Fast Flow resin (GE Healthcare), which had been equilibrated in binding buffer. Soluble cell lysate and Ni resin were left on a mixing platform at room temperature for 1 h, before the resin was loaded into a disposable chromatography column (BioRad). Using gravity flow, the Ni resin was washed with 20 mL of wash buffer (20 mM Tris pH 8.0, 500 mM sodium chloride, 1 mM TCEP, 116 mM imidazole) and the CoaD was eluted from the column using 10 mL elution buffer (20 mM Tris pH 8.0, 500 mM sodium chloride, 1 mM TCEP, 500 mM imidazole).
To remove co-purified coenzyme A (CoA) from the CoaD active site, purified protein was concentrated to a volume of 500 μL in a 10 kDa Amicon Ultra centrifugal filter unit (Millipore) and resuspended to 10 mL using dialysis buffer (20 mM sodium citrate pH 5.0, 1 mM TCEP). This process was repeated three times. The protein solution was then placed into a 3 mL 10 kDa Slide-A-Lyzer dialysis cassette (Thermo Fisher Scientific) and dialyzed against 2 L of dialysis buffer for 48 h, with the buffer being exchanged every 24 h. The extent of CoA present in the sample was assessed by measuring the ratio of absorbance at 260 and 280 nm under native and thermal denaturing conditions (Geerlof et al. 1999).
The CoA free CoaD was exchanged into NMR buffer [20 mM sodium phosphate pH 7.0, 1 mM deuterated dithiothreitol (DTT)] using a PD-10 column (GE Healthcare) which had been pre-equilibrated in NMR buffer. Samples were concentrated to a final monomeric concentration of 350 μM, flash frozen in liquid nitrogen and stored at −80 °C until needed. Samples used for the 4D methyl–methyl 13C-resolved HMQC–NOESY–HMQC experiment were lyophilized overnight and resuspended in an equal volume of 100 % D2O (CIL).
NMR experiments
All NMR experiments were conducted with 160 μL of sample in a 3 mm NMR tube and were recorded at 308 K on a Bruker AVANCE III 600 MHz spectrometer equipped with a 5 mm CP-QCI z-gradient probe. Due to only labeling the methyl groups and along with the highly deuterated nature of our samples, we were able to utilize the increase in sensitivity obtained from measuring 2D [13C, 1H]-methyl TROSY experiments (Tugarinov et al. 2003). 2D [13C, 1H]-HMQC SOFAST (Schanda et al. 2005) experiments were acquired with an excitation flip angle of 100° and a proton band width of 3 ppm, centered at 1 ppm. Experiments were recorded using either uniform or 50 % non-uniform sampling with a recycle delay of 200 ms collecting a total of 1024 and 256 points in the direct and indirect dimensions, respectively. Spectra were processed using a QSINE window function, with 1.0 and 0.3 Hz line broadening applied in the direct and indirect dimensions, respectively. The 4D methyl–methyl 13C-resolved HMQC–NOESY–HMQC experiment was recorded using 25 % non-uniform sampling (Tugarinov et al. 2005) with a mixing time of 120 ms. A total of 32,488 points were collected across all three indirect dimensions and 1024 points collected in the direct proton dimension. All non-uniformly sampled experiments were acquired with Poisson Gap sampling schedules (Hyberts et al. 2010), and were processed in Topspin 3.2 using either the hmsIST algorithm (Hyberts et al. 2012) for 2D-[13C, 1H]-SOFAST HMQC experiments or Multi-Dimensional Decomposition (MDD, Bruker) for the 4D 13C-resolved HMQC–NOESY–HMQC experiment.
Calculation of equilibrium dissociation constants
K d values for ligand binding were calculated by titrating between 12.5 μM and 5 mM ligand into a 50 μM sample of MILVAT labeled CoaD and measuring 2D [13C, 1H]-SOFAST HMQC experiments. The weighted change in chemical shift (Δ) of peaks, when compared to the apo spectrum of CoaD, was calculated using a 13C scaling factor of 0.25 and the following formula was used to fit the data to calculate K d values:
where Δ corresponds to the observed weighted change in chemical shift at a given total ligand concentration [L] T , \(\Delta_{max}\) is the change in chemical shift at saturation and [P] T is the total protein concentration.
Computation of methyl–methyl distances
Average distances between methyl groups of different amino acids of interest were computed using a Perl script. The script requires a protein data bank (PDB) file of the protein structure as input, as well as a list of the amino acids and the atoms of interest to be used in the analysis. The Perl script then determines carbon–carbon pairwise distances between all atoms of interest. Pairs of atoms separated by a distance above a user defined cut-off value are not considered. In the case of multimeric assemblies, distances for the same atom pairs in different subunits are averaged to account for small structural variations.
Results and discussion
The protein of interest used in this study is the E. coli phosphopantetheine adenylyltransferase CoaD, which natively exists as a 115 kDa homohexamer (Fig. 1). CoaD catalyzes the magnesium dependent transfer of an adenylyl group from ATP to 4′-phosphopantetheine to generate dephospho-CoA, which is an intermediate in the biosynthesis of coenzyme A (CoA) (Geerlof et al. 1999). CoA is an essential enzyme cofactor in all living organisms and plays a central role in reactions involved with cellular metabolism as well as fatty acid, polyketide and non-ribosomal peptide biosynthesis (Leonardi et al. 2005; Spry et al. 2008). For this reason and due to the limited conservation between the bacterial and human forms of the enzyme, CoaD is also of interest as a potential antibacterial drug target (Aghajanian and Worrall 2002; Daugherty et al. 2002; Miller et al. 2007). Analysis of the protein amino acid sequence shows that methyl containing amino acids constitute 44 % of the polypeptide sequence and are distributed evenly throughout the structure (Fig. 1). The enzyme has been both biochemically and structurally characterized exhaustively, and as a result a number of structures, both in the absence and presence of inhibitors as well as natural products are already available in the PDB (Izard and Geerlof 1999; Izard 2002, 2003; Miller et al. 2007).
Production of MILVAT labeled protein
The goal of the research presented here was to produce a protocol to simultaneously label all six methyl containing amino acids. In order to see if this could be achieved, CoaD samples where the six methyl containing amino acids were labeled individually (M, I, A) or in their respective pairs (LV, IT) were produced as a benchmark for comparison to a MILVAT labeled sample. A sample of LV protein was also produced in the presence of 20 % BioExpress to suppress the incorporation of label at leucine Cδ positions (Tzeng et al. 2012). [13C, 1H]-SOFAST-HMQC experiments sampling the methyl region were acquired using 50 µM samples of each selectively labeled protein. The resulting individual spectra are shown in Supplementary Fig. 1, and a composite HMQC spectrum containing a superposition of the individual spectra, colored according to amino acid type, is shown in Fig. 2a. All 103 expected peaks are present in the spectra and only a minimal amount of overlap is observed between the leucine δ1 and δ2 and valine γ1 and γ2 resonances.
A MILVAT labeled protein sample was produced by resuspending all six precursors and labeled amino acids (Table 1) in D2O and adding this solution to the E. coli growth 1 h prior to induction. A [13C, 1H]-SOFAST-HMQC experiment acquired with 50 μM MILVAT labeled protein (Fig. 2b) shows that simultaneous labeling of all six amino acid methyl groups achieves an identical HMQC spectrum to the composite spectrum produced from the individually labeled protein samples (Fig. 2a). In addition, a [13C, 1H]-HMQC spectrum covering the full aliphatic and aromatic regions of the spectrum was acquired with folding in the indirect dimension (Supplementary Fig. 2). Even when analyzed at the level of the noise, the only significant peaks present in the spectrum are those of the resonances specifically labeled using MILVAT labeling. A single threonine resonance (1H 0.96 ppm, 13C 21.31 ppm), which overlaps with two leucine δ resonances, is not resolved in the MILVAT spectrum, however the presence of a threonine peak at this position was confirmed using a 4D HMQC–NOESY–HMQC experiment.
Analysis of scrambling into unwanted methyl positions
Previous reports published by Ayala et al. and Kerfah et al. concluded that scrambling into multiple amino acid side chains, including isoleucine at the Cγ2 position, was observed when supplementing the medium with alanine, selectively labeled at the Cβ position (Ayala et al. 2009; Kerfah et al. 2015b). Figure 3a shows the HMQC spectrum of a MILVAT labeled sample, along with a magnified area corresponding to the region of the spectrum where we would expect to see isoleucine Cγ2 resonances. Even when plotting the spectrum at the level of the noise, no unexpected peaks are present in the spectrum, indicating that there is no scrambling into the isoleucine Cγ2 position in the MILVAT labeled protein sample. Even though inclusion of 100 mg/L of selectively labeled alanine during expression is sufficient to label all alanine Cβ resonances (see below), the lack of scrambling could have been attributed to the relatively low concentration of labeled alanine included during protein expression (Table 1). To address this, we performed similar analyses with protein samples expressed with higher concentrations of labeled alanine (up to 700 mg/L), and again no undesired incorporation into the isoleucine Cγ2 position was observed. Scrambling has also been reported to occur from alanine into the valine and leucine Cγ and Cδ positions, respectively (Ayala et al. 2009; Godoy-Ruiz et al. 2010; Kerfah et al. 2015b); however, we are not concerned about any potential scrambling into these positions as these atoms are intentionally labeled in this protocol.
Probing the extent of isotope incorporation
In addition, Ayala et al. also observed a correlation between the concentration of labeled alanine added prior to induction and the incorporation of selective label at the alanine Cβ position (Ayala et al. 2009; Kerfah et al. 2015b). The concentration dependence of alanine required to achieve complete incorporation in our system was addressed using ILVA growths where different concentrations of alanine (100, 200 and 700 mg/L) were supplemented into the medium 1 h prior to induction. All samples were purified in the same way and 2D [13C, 1H]-SOFAST HMQC experiments were acquired on protein solutions of the same concentration using identical acquisition parameters. The peaks corresponding to alanine residues were picked in all three spectra and their absolute intensities were determined (Fig. 3b). There is no difference observed between the intensities of alanine residues in samples which were supplemented with different concentrations of alanine prior to induction, indicating that the same degree of alanine incorporation is achieved in all three samples. With this in mind, we decided to supplement our minimal medium with 100 mg/L of selectively labeled alanine for all future experiments. When comparing the different protocols, differences are apparent in the carbon sources used for bacterial growth and protein expression. Ayala et al. use protonated glycerol as the sole carbon source, while Kerfah et al. use deuterated 12C glucose (Ayala et al. 2009; Kerfah et al. 2015b). Our protocol uses protonated 12C glucose as the predominant carbon source (additional carbon is supplemented into the medium in the form of selectively labeled precursors and amino acids) and although this may slightly decrease the total extent of deuteration of the protein, it does not appear to significantly affect the quality of the spectrum produced. Although this is a major difference between the three protocols, there are also other subtle variations in the expression protocols including concentrations of IPTG used along with the applied temperatures and lengths of time used for protein induction which could also contribute to the differences observed.
To quantitatively assess overall isotope incorporation, we performed mass spectrometry analysis on the MILVAT labeled CoaD protein. The expected mass is 20,239.8 Da, assuming that all amide bound protons have exchanged with H2O and that all methyl containing amino acids are fully labeled. The experimentally determined molecular weight peaks at 20,143.7 Da (Supplementary Fig. 3), which equates to a difference in molecular weight of 96 Da. This corresponds to approximately one proton being incorporated into each amino acid that is not selectively labeled on average. An asymmetric mass distribution of approximately 140 Da is observed around the average mass, which presumably arises from different degrees of amide back exchange along with incorporation of protons from water present in D2O and the protonated glucose. Our experimental data indicates that isotope incorporation of greater than 99 % can be achieved using the outlined protocol, however, if higher levels are required the use of deuterated 12C-glucose could be considered.
To analyze if preferential incorporation of supplemented amino acids or precursors into one amino acid over another was obtained, all peaks present in the [13C, 1H]-HMQC spectrum of the MILVAT labeled protein (Fig. 2b) were picked and their intensities were determined. Peaks were sorted according to their intensity and a profile for all peaks was generated (Fig. 3c; Pedrini et al. 2013). With exception of the first 15 peaks, which have a high intensity as a result of being surface exposed or present in a mobile area of the protein, all CoaD methyl peaks have a fairly even intensity, and do not abnormally cluster according to amino acid type in the intensity profile. This indicates that we see an equal incorporation of isotopes into all six amino acid types.
When compared to the individually labeled protein samples, a small decrease in methyl signal intensity was observed in the case of CoaD upon labeling all six amino acids. This effect could be attributed to line broadening due to enhanced relaxation caused by the increased number of NMR active probes in the sample (e.g. illustrated in Kerfah et al. 2015c). To assess this, the linewidths of all sufficiently isolated peaks were determined in the extracted 1D rows of the HMQC spectra. When all six amino acids were labeled individually, the average linewidth of all peaks analyzed was 16.0 Hz. As expected, upon increasing the number of labels present in the sample, line broadening is observed for all amino acid types (Table 2). When compared to the single labeled samples (M, I, A), peaks corresponding to the same residues in the MILVAT labeled protein sample have an increased linewidth of approximately 1.8 Hz (Table 2). For samples where amino acids are labeled as pairs (LV, IT), the increase in linewidth observed in the MILVAT labeled protein is approximately 0.7 Hz. A respective increase in linewidth between 0.8–1.0 and 0.4–0.8 Hz is observed for peaks when comparing MILVAT labeling to the standard ILV and ILVA labeling schemes (Table 2). Although these numbers are expected to vary between different protein systems, the data presented here suggests that the benefits obtained from having all six methyl groups labeled simultaneously can outweigh the increase in spin relaxation, especially when compared to that already observed with an ILVA labeling scheme.
Using the described protocol, to date we have successfully labeled and analyzed multiple homo-multimeric proteins with the size of the molecular assemblies ranging between 45 and 150 kDa. For all proteins analyzed, there was no scrambling into unwanted positions and a general increase in signal linewidth was observed as detailed above. However, in some of the systems studied, a larger decrease in signal intensity was observed for a subset of threonine signals when compared to the decrease observed for other peaks in the spectrum. This may be a combined result of the increased proton density along with the dynamics and conformational exchange occurring in the proteins analyzed (Velyvis et al. 2012).
Assignment of methyl groups using a single 4D 13C-resolved HMQC–NOESY–HMQC experiment
When selective labeling of methyl groups in proteins is required, the standard labeling schemes used are either ILV or ILVA labeling. A comparison of MILVAT labeling to these standard labeling protocols indicates that the increase in probe coverage obtained from selectively labeling all six methyl containing amino acids would facilitate assignment of all methyl groups using a single 4D 13C-resolved HMQC–NOESY–HMQC experiment. Previously, the strategy of consecutively assigning neighboring methyl groups through NOE connectivities (‘methyl walk’) might have been limited since many distances between labeled probes exceed the detection limit of a NOESY experiment. In the MILVAT labeled protein sample, NMR active nuclei are now much more likely to be present in these gaps, thus allowing the user to ‘walk’ from methyl to methyl and assign the peaks based on the known structure of the protein. To demonstrate the feasibility of an efficient methyl walk using MILVAT-labeled protein, a 4D 13C-resolved HMQC–NOESY–HMQC experiment, which had been resolution optimized so only the methyl region in the indirect proton dimension was sampled, was implemented. Using the crystal structure of apo CoaD (PDB entry 5JBN), the intra- and inter-molecular distances between the carbon atoms of methyl groups in the protein monomer and any symmetry pairs in the oligomeric unit were calculated. An upper distance limit of 7.5 Å was imposed while conducting the analysis to simulate the expected maximum nuclear Overhauser effect (NOE) observable distance, as well as to accommodate for the additional distance of the attached proton atoms, which is not accounted for in the analysis.
The 4D methyl–methyl 13C-resolved HMQC–NOESY–HMQC experiment was analyzed by evaluating cross peaks present in the (F3, F4) HMQC plane with the F2 and F1 dimensions set to the frequencies of the methyl resonance being assessed (Fig. 4). Using the beforehand determined amino acid type assignments, we were able to go through the spectrum and generate a network of interactions observed by each methyl group in the sample. By comparing this list of observed methyl NOEs to the output of expected methyl NOEs, we were able to find multiple patterns which are unique to particular methyl groups. Such patterns then served as starting points from which we could conduct a series of methyl walks to assign the surrounding methyl groups (Fig. 4). For the purposes of the work being conducted, the complete assignment of the protein was not required, however using a single MILVAT labeled sample, along with the information obtained from the individually labeled protein preparations, we were able to confidently assign 60 % of all methyl groups in CoaD, which included the complete enzymatic pocket as well as residues immediately surrounding that area, within one day. Interestingly, all six different methyl containing amino acids are found in the active site (Supplementary Fig. 4) and the simultaneous labeling of all amino acids greatly facilitated the assignment due to the absence of gaps in the methyl–methyl network.
Interaction studies with (R)-pantetheine
In addition to facilitating resonance assignment, the increased probe density in a MILVAT labeled protein also enables the study of structure–function relationships with greater detail and accuracy. For example, the binding site of a ligand could be more comprehensively captured in a single mapping experiment. To demonstrate this, we assessed the binding of the substrate analogue (R)-pantetheine by monitoring chemical shift perturbations of protein methyl groups. A crystal structure of E. coli CoaD in complex with 4′-phosphopantetheine [PDB entry 1QJC, (Izard 2002)] shows that the binding site covers one side of the complete enzymatic pocket which is partially comprised of residues from the neighboring subunit in the hexameric holoenzyme (Fig. 5a). Since the reported K d for phosphopantetheine is 270 nM (Miller et al. 2007), we chose the analogue (R)-pantetheine for our binding study in order to form a weaker interaction which would be in fast exchange. A 50 μM sample of MILVAT labeled CoaD was measured with increasing concentrations of (R)-pantetheine up to a final concentration of 5 mM. Addition of (R)-pantetheine to the sample induced chemical shift perturbations in the spectrum, indicating that the substrate analogue interacted with CoaD (Fig. 5b) in the fast exchange regime. The changes in chemical shift of multiple peaks in the spectrum were used to determine a K d of 1.6 ± 0.3 mM. Analysis of the assignments of peaks in the spectrum which exhibited the largest changes in chemical shift showed that methionine, leucine, valine and alanine residues are affected and that those peaks corresponded to methyl groups which are directly surrounding the ligand. Additional smaller perturbations are observed in second shell and more remote residues upon addition of a ligand which is consistent with the observations made by others that CoaD is an allosteric enzyme (Izard 2002). The increased number and type of affected peaks observed by employing the new labeling scheme will allow characterization of these processes in more detail, e.g. by magnetization relaxation based dynamics studies.
Conclusions
We have developed a protocol for the selective, simultaneous labeling of all methyl groups (except Ile Cγ) in the six methyl containing amino acids and have demonstrated how such a sample can be used to facilitate the assignment of methyl groups in the enzyme CoaD. The simultaneous labeling of all six amino acids does not adversely affect the spectral quality of CoaD and the addition of selectively labeled threonine, alanine and methionine resonances hardly increases the amount of peak overlap due to the unique places in the spectrum where these resonances appear. There are significant benefits of observing all six amino acids simultaneously in the spectrum, especially when using NOESY datasets to assign peaks, since the unique chemical shift fingerprints of peaks obtained from having methionine, alanine and threonine labeled help when trying to identify unique starting points or when trying to unambiguously assign peaks.
There are currently a number of different computational programs that conduct the assignment of methyl groups using the information from multi-dimensional NOESY datasets, however, these programs generally need to be supplemented with additional experimental data in order to increase the quantity of or confidence in the unambiguous assignments made (Chao et al. 2014). It is our belief that the use of both 4D spectroscopy and MILVAT labeling would greatly increase the performance of programs which work to produce a complete methyl assignment based on identifying networks of methyl–methyl NOEs in multidimensional NOESY datasets, without having to supplement the analysis with additional experimental data.
Isolated methyl groups that are not present in a methyl–methyl network cannot be assigned directly using this process, however if these groups are required for the analysis being conducted, often they can be assigned through the process of elimination. In most cases where structures are not being calculated, a complete assignment of all methyl groups is not needed and research groups are only interested in the subset of peaks from residues within a protein active site or binding interface which are involved in the reaction or interaction being studied. The use of MILVAT labeling offers multiple unique starting points in the 4D NOESY dataset from which methyl walks can be conducted, facilitating the assignment of only the regions of interest. When compared to the standard ILV or ILVA labeled samples, the percentage of methyl groups labeled in a MILVAT sample increases on average to 35 % from 18 and 27 %, respectively (Miller et al. 1987; Conte et al. 1999). This increased number of NMR active probes in the sample significantly increases the redundancy observed in the NOESY dataset, thus providing increased confidence in the assignments made. In addition to the total increase in the number of NMR active probes present in the sample, a 2.3 or 1.4 fold increase in the number of probes available on the protein surface is observed in a MILVAT labeled sample, when compared to the standard ILV or ILVA labeling scheme, respectively (Miller et al. 1987). Extending selective labeling to include methionine and threonine is of particular interest because of the unique flexible aliphatic thioether moiety and polar hydroxyl group in their respective side chains. These features often allow for productive interactions on the protein surface and in ligand binding sites, whereas isoleucine, leucine and valine side chains are generally found in the hydrophobic core.
The increased number of probes in a protein’s active site enables a more detailed structural characterization of molecular interactions, which is of particular interest when studying protein small molecule complexes due to the highly localized binding event. Additional intermolecular NOEs measured to unambiguously assigned methyl groups are important to reduce the possible binding modes and ligand conformations in order to obtain models with reasonable confidence. As NOE-derived intermolecular distance information is preferably obtained from a single sample, MILVAT labeling is essential for any form of structural analysis using NOESY experiments. In addition to the benefits offered for such structural and interaction studies, the use of MILVAT labeling is also advantageous for groups interested in protein dynamics, conformational analysis, methyl detected relaxation dispersion and paramagnetic relaxation enhancement. Although for such experiments similar results could be achieved from studying multiple different samples, MILVAT labeling allows all information to be collected simultaneously and analyzed using a single sample, thus leading to both financial and time savings as well as to a simplification of analysis without having to compensate for sample variation.
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Acknowledgments
The authors would like to thank Dr. Clemens Anklin and Dr. Eric Johnson at the Bruker BioSpin Corporation for their assistance with the implementation of the 4D methyl–methyl 13C-resolved HMQC–NOESY–HMQC experiment, Dr. Lili Xie and Kyoko Uehara for their help in designing the purification protocol for CoaD, and Dr. Dirksen Bussiere for his assistance with refinement of the CoaD structure. All images produced of the CoaD structure were done so using Pymol (Schrödinger, LLC 2015).
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AP, AOF, FR, MM and AL are employees of Novartis.
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Proudfoot, A., Frank, A.O., Ruggiu, F. et al. Facilitating unambiguous NMR assignments and enabling higher probe density through selective labeling of all methyl containing amino acids. J Biomol NMR 65, 15–27 (2016). https://doi.org/10.1007/s10858-016-0032-2
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DOI: https://doi.org/10.1007/s10858-016-0032-2