Resonance assignment of intrinsically disordered proteins is remarkably challenging due to scant chemical shift dispersion arising from conformational heterogeneity. The challenge is even greater if repeating segments are present in the amino acid sequence. To forward unambiguous resonance assignment of intrinsically disordered proteins, we present iHACANCO, HACACON and (HACA)CONCAHA, three Hα-detected 4D experiments with Cα as an additional dimension. In addition, we present (HACA)CON(CA)NH and (HACA)N(CA)CONH, new 4D Hα-start, HN-detect experiments which have two NH dimensions to enhance peak dispersion in a sequential walk through C′, NH and HN, and provide more accurate NH/HN chemical shifts than those that can be obtained from a crowded 1H, 15N-HSQC spectrum. Application of these 4D experiments is demonstrated using BilRI (165 aa), an outer-membrane intrinsically disordered protein from the opportunistic oral pathogen Aggregatibacter actinomycetemcomitans. BilRI amino acid sequence encompasses three very similar repeats with a 13-residue identical stretch in two of them.
Aggregatibacter actinomycetemcomitans is a Gram-negative opportunistic oral pathogen that is linked to periodontitis, infection of tissues supporting the teeth (for reviews, see Fine et al. 2006; Åberg et al. 2015; Fine et al. 2019). Although A. actinomycetemcomitans resides in subgingival multispecies biofilms, it is also able to migrate to underlying vessels and cause systemic diseases such as cardiovascular diseases (Kozarov et al. 2005; Hyvärinen et al. 2012). The host response to biofilms is mediated by inflammatory cytokines. In healthy junctional epithelium of tooth the balance of various cytokines and chemokines ensures that the host defence works appropriately. Some periodontal pathogens are able to impair the balance. Porphyromonas gingivalis can suppress the expression of chemokine interleukin(IL)-8 (Takeuchi et al. 2013) and A. actinomycetemcomitans biofilm is able to sequester and internalize IL-1β, IL-8 and IL-6, which leads to changes in biofilm composition and metabolic activity (Paino et al. 2011, 2012; Ahlstrand et al. 2017). It has been suggested that A. actinomycetemcomitans bacterial IL receptor I, BilRI is associated with this sequestering activity (Paino et al. 2013; Ahlstrand et al. 2017). BilRI is an outer membrane lipoprotein able to bind IL-1β, IL-8 and IL-10 and tumor necrosis factor (TNF)-α (Ahlstrand et al. 2017). Due to its rather low binding affinity it is assumed that BilRI acts by concentrating cytokines on cell membranes, which are then transferred to other components of the uptake system (Paino et al. 2013; Ahlstrand et al. 2017). We have engaged in the structural characterization of BilRI.
BilRI is an intrinsically disordered protein (IDP), as demonstrated by its 1H, 15N HSQC spectrum, which displays very limited signal dispersion (Ahlstrand et al. 2017). In the HN dimension their dispersion is only 0.63 ppm. This arises from a feature typical of IDPs, namely a biased amino acid composition with a pronounced number of polar or charged amino acids, low number of bulky hydrophobic amino acids and lack of aromatic amino acids (Dyson 2016). BilRI amino acid sequence is dominated by alanine (23%), lysine (14%) and aspartic acid (13%) residues. However, unlike the general trend (Dunker et al. 2001), BilRI sequence contains only one proline and one glycine. BilRI is positioned among IDPs in the mean net charge-hydropathy plot (Uversky et al. 2000) (Fig. 1a). The paucity in the variability of residue’s nearest neighbors narrows down the chemical shift range of a particular amino acid type, for example there are 12 Lys-Asp-Ala triplets in the sequence, which most likely results in close chemical shifts for the middle aspartic acid. Additionally, the BilRI sequence contains three very similar segments of about forty residues. The longest identical stretch is of 13 residues, present in two of these repeats, covering residues 71–82 and 111–122 (Fig. 1b).
The 1H, 15N HSQC spectra of IDPs typically being very challenging to scrutinize, the resonance assignment most often relies on spectra other than the classical HN-detected experiments widely used for folded proteins (for reviews see e.g. Sattler et al. 1999; Permi and Annila 2004). Indeed, the conventional approach based on the HNCACB and HN(CO)CACB/CBCA(CO)NH experiments that link the intra- and sequential 13Cα and 13Cβ chemical shifts to 1HN and 15N frequencies, are very inefficient for many IDPs due to severe clustering of aliphatic carbon chemical shifts for each residue type. Instead, correlation of 15N and 13C′ frequencies provide much better results for IDPs (Yao et al. 1997; Mäntylahti et al. 2009; Bermel et al. 2012) Another obstacle arises from the increasing chemical exchange rate of amide protons with water at alkali pH and/or elevated measurement temperature (Mäntylahti et al. 2010). Yet another challenge for the assignment originates from the abundancy of proline residues in IDPs. As an N-substituted residue, proline lacks the amide proton, which results in gaps during the resonance assignment procedure. Although this can be a benefit in the case of globular proteins, it significantly hampers the resonance assignment of disordered systems (Hellman et al. 2014). Several different approaches have been proposed to overcome these obstacles imposed during the assignment procedure. These include increase of dimensionality from conventional 3D to 4–7D spectra (Fiorito et al. 2006; Motáčková et al. 2010; Nováček et al. 2011; Kazimierczuk et al. 2013; Brutscher et al. 2015) as well as detection of non-exchangeable spins 13C′ and 1Hα instead of 1HN (Bermel et al. 2006a, 2009; 2012; Mäntylahti et al. 2010, 2011; Permi and Hellman 2012). Our group has been resorting both to Hα-start, HN-detect pulse schemes (Mäntylahti et al. 2009; Hellman et al. 2014) or complete Hα-detection experiments (Mäntylahti et al. 2010, 2011; Permi and Hellman 2012) for the assignment of IDPs, which overcome hurdles associated with proline assignment and exchange broadening at alkali pH or elevated temperature. In addition to reduced susceptibility towards solvent exchange induced linebroadening, the Hα chemical shift is extremely valuable in structural analysis. The Cα, Hα and C′ shifts are particularly sensitive to the ϕ/ψ angles of the protein backbone and thus the most informative in the estimation of secondary structure content in an IDP (Borcherds and Daughdrill 2018).
Comprehensive assignments allow for detailed, residue-specific analysis of structure and dynamics (Konrat 2014). There are therefore grounds for an extra effort towards a more comprehensive backbone resonance assignment. IDPs are often comprised of repetitive amino acid sequences and hence higher dimensionality in combination with high resolution offer superior results. However, the increased dispersion of signals should not be obtained, if possible, at expense of sensitivity. Here we present the resonance assignment of BilRI, whose demanding amino acid sequence necessitated development of a suite of 4D pulse sequences that offer superior signal dispersion with respect to their well-established 3D counterparts without indirect sampling associated sensitivity loss.
Materials and methods
Protein expression and purification
The gene encoding BilRI (residues 21–181) was cloned to pET15b vector (Novagen) into the NdeI and XhoI sites. This leads to soluble recombinant BilRI protein with N-terminal His-Tag with a thrombin cleavage site.
Production of 13C, 15N labeled BilRI was carried out by transforming plasmids into the BL21(DE3) cells. Cells were grown in M9 minimal media, supplemented with 1 g/l of 15NH4Cl and 2 g/l 13C-d-glucose as the sole nitrogen or nitrogen and carbon source, respectively. Cell culture was incubated at 37 °C and temperature was decreased to 16 °C when OD of the cell culture reached 0.4 and protein production was induced with 1 mM IPTG when OD of the cell culture reached 0.6. Cells were further incubated at 16 °C for 16 h and collected by centrifugation. Cells were disrupted with sonication and resulting supernatant was clarified by centrifugation with 30,000×g.
Clarified supernatant of BilRI was applied to the 1-mL His GraviTrap column (GE Healthcare) and the His-Tag was removed by thrombin protease (GE Healthcare) digestion according to the manufacturer’s instructions. Protease digested mixture was applied to His GraviTrap column. BilRI, without His-Tag, eluted with flow-through. Flow-through was concentrated to volume of 1 ml with Vivaspin 2 concentrator. Concentrated BilRI sample was applied into the Superdex 75 16/60 gel filtration column (GE Healthcare). Buffer used in gel filtration contained 20 mM sodium phosphate (pH 6.5) and 50 mM NaCl (NMR buffer). Fractions with pure BilRI were pooled and concentrated for NMR studies. The gel filtration was performed by using the ÄKTA Purifier FLPC purification system (GE Healthcare).
BilRI NMR experiments were acquired using 0.5–1.0 mM 15N, 13C labeled protein samples in 5/95% D2O/H2O at pH 6.5. Chemical shifts were referenced to external 2,2,-dimethyl-2-silapentane-5-sulfonic acid (DSS). All data were acquired at 25 °C on a Bruker AVANCE III HD 800 MHz spectrometer, equipped with a TCI 1H/13C/15N cryoprobe. In addition to the new 4D experiments described here, the following experiments were used in the resonance assignment: 2D 1H, 15N-HSQC, constant time 1H, 13C-HSQC, 13C-detected 2D CON (Bermel et al. 2006b), 3D HN-detected HNCACB, CBCA(CO)NH, HNCO (reviewed in (Sattler et al. 1999; Permi and Annila 2004) and i(HACA)CO(CA)NH (Mäntylahti et al. 2009), 3D Hα-detected HA(CA)CON, iHA(CA)NCO and (HACA)CON(CA)HA (Mäntylahti et al. 2010, 2011). All 3D/4D experiments were collected using non-uniform sampling (Table 1). Sampling densities were 25% for the 3D experiments and 7–20% for the 4D experiments. NMR data were processed with TopSpin 3.5 (Bruker Inc) and analyzed with CcpNmr Analysis v. 2.4.2 (Vranken et al. 2005). BilRI chemical shifts have been deposited to the BMRB database (www.bmrb.wisc.edu) with accession code 27824.
Results and discussion
Peaks in the BilRI 2D 1H, 15N-HSQC spectrum display overwhelming overlap (Fig. 2a) and a very narrow distribution in the HN dimension. As it was later revealed, all but three of the 21 aspartic acid residues’ peaks are located in the middle region pile of peaks, 8.27–8.38, 121.2–121.9 ppm, together with 11 of the 13 methionine residues’ amide peaks. The Asp and Met α signals heavily overlap also in the 1H, 13C CT-HSQC (Suppl. Fig. S1). The CON spectrum, on the other hand, shows remarkably well dispersed signals (Fig. 2b) with peaks from all C′–NH pairs present. We thus first attempted the assignment with spectra having the CON spectrum as the root spectrum, namely Hα-detected experiments HA(CA)CON, iHA(CA)NCO and (HACA)CON(CA)HA (Mäntylahti et al. 2010, 2011). 3D HN-detected experiments HNCACB, CBCA(CO)NH, HNCO and i(HACA)CO(CA)NH (Mäntylahti et al. 2009) were acquired to collect HN, C′, Cα and Cβ chemical shifts. With this set of seven 3D spectra, we assigned the majority of backbone resonances. However, there were several ambiguous assignments, in particular within the aforementioned repeating segments. Moreover, while precise Hα and C′ shifts were obtained from the 3D Hα-detected experiments and the CON, due to heavy overlap, Cα/Cβ shifts were far more difficult to read from the HNCACB and CBCA(CO)NH spectra. Indeed, a precise Cα/Cβ chemical shift for 66% of the residues was obtained, while for Hα, resolved peaks for 87% of the residues were observed (Suppl. Fig. S2).
To resolve these ambiguities and to extend the number of accurate chemical shifts, we resorted to 4D NMR spectroscopy. In order to bypass the Cα overlap problem in 3D HN-detected experiments and to establish direct connectivities between Hα and Cα, and to provide dispersion to solve ambiguities arising from occasional overlap of C′, Hα resonances encountered in the 3D Hα-detected experiments, we devised Hα-detected 4D experiments with Cα as an additional dimension. In addition, we developed and employed new 4D Hα-start, HN-detect experiments which can bridge stretches over single prolines similar to 3D experiments described in Hellman et al. (2014), but which have two NH dimensions to enhance peak dispersion in a sequential walk through C′, NH and HN, and to provide for more accurate NH/HN chemical shifts than those that could be obtained from the crowded regions of the 1H, 15N HSQC.
4D iHACANCO, HACACON and (HACA)CONCAHA experiments
The proposed 4D iHACANCO, HACACON and (HACA)CONCAHA experiments are extensions of their established 3D counterparts (Mäntylahti et al. 2010, 2011) with additional sampling on the fourth 13CA dimension (Fig. 3). The coherences flow through the 4D iHACANCO, HACACON and (HACA)CONCAHA experiments in Eqs. 1, 2, 3:
respectively. All experiments start with the 1Hα(i)→ 13Cα(i) transfer, and the density operator immediately after the ϕ3 pulse is described as Hαz(i)Cαz(i) (time point a). Subsequently, the magnetization is transferred to the 13C′ spin followed by the labeling of 13C′ chemical shift in t1 or t2. The relevant density operator after the ϕ2 pulse in all experiments is described as Cαz(i)C′y(i) (time point b). Next, the desired coherence is transferred to the 15N spin of the sequential residue in HACACON and (HACA)CONCAHA experiments, described with the density operator Cαz(i)C′z(i)Ny(i + 1) (time point c). In the iHACANCO experiment, the magnetization is solely transferred to the 15N spin within the residue, described with the density operator Cαz(i)C′z(i)Ny(i) (time point c). After labeling the 15N chemical shifts in t1 (or t2), the magnetization is transferred to the 13Cα coherence after the ϕ4 pulse. The relevant density operators (time point d) are Cαy(i)Nz(i) for iHACANCO, Cαy(i)C′z(i) for HACACON and Cαy(i)Nz(i) for (HACA)CONCAHA schemes. The 13Cα chemical shift is labeled during the t3 period between time points d–e.
While the HACACON (Fig. 3b) is the conventional out-and-back experiment, the (HACA)CONCAHA and iHACANCO utilize the intraresidual filter for the selective 13Cα(i)→ 15N(i) transfer (Permi 2002; Mäntylahti et al. 2010, 2011). Especially in the iHACANCO experiment, the magnetization transfer is nested and further clarification is delivered in the following. After converting magnetization to the Hαz(i)Cαz(i) coherence (time point a), the 1JCαC′, 1JCαN, 2JCαN and 1JCαCβ couplings are active during the time interval (2TC + 2TA + 2TC′ + TCC) = 52–57 ms, which converts it to the Cαz(i)Ny(i) coherence (time point c). However, during the delay 2TCC, that can be selected to be 0–5 ms based on the relaxation properties of 13Cα spins, only 1JCαCβ is active. This is to maximize the transfer efficiency during the (2TC + 2TA + 2TC′ + TCC) delay. Of note, to avoid chemical shift evolution of 13Cα–13C′ multiple-quantum coherence during 2TA –t2, an additional but opposite frequency labeling period for 13Cα has been implemented in the 2TC′ period. Efficiently, only the chemical shift evolution of 13C′ will take place during t2, but the attainable resolution is limited by 2TC′ (= 2TC + TCC) i.e. t2,max is 19–22 ms, depending on the setting of 2TCC (0–5 ms).
Thus, the 4D iHACANCO, HACACON and (HACA)CONCAHA experiments yield correlations at ωHA(i), ωCA(i), ωC′(i), ωN(i); ωHA(i), ωCA(i), ωC′(i), ωN(i+1), and ωHA(i), ωCA(i), ωC′(i–1), ωN(i) frequencies, respectively. Given that frequency labeling of 13Cα chemical shifts is implemented in a constant-time manner, without lengthening the actual pulse sequence and incorporating sensitivity enhanced gradient echo in t3, there is no sensitivity loss involved in increasing the dimensionality of these Hα-detected experiments. Hence, the coherence transfer efficiencies provided with the corresponding 3D experiments by Mäntylahti et al. (2010, 2011) are directly comparable to 4D implementations shown in Fig. 3. Indeed, by taking into account typical values of one-bond couplings 1JCαC′ = 53 Hz, 1JC′N = 15 Hz, and 1JCαCβ = 35 Hz, and the average random coil values for one-bond (1JCαN = 10.6 Hz) and two-bond (2JCαN = 7.5 Hz) couplings between backbone 13Cα and 15N spins (Delaglio et al. 1991), as well as transverse relaxation times (T2) for 13Cα (= 100 ms), 13C′ (= 200 ms) and 15N (= 200 ms) spins, we can estimate coherence transfer efficiencies for these experiments in IDPs (Mäntylahti et al. 2010, 2011). The HACACON is superior in sensitivity (I ~ 0.28) in comparison to iHACANCO and (HACA)CONCAHA experiments, with coherence transfer efficiencies of 0.22 and 0.18, respectively. Particularly, for the assignment of prolines, sensitivities of iHACANCO and HACACON are superior to the (HACA)CONCAHA scheme, which yields coherence transfer of 0.026 for proline residues. The sensitivity loss is associated with the 15N(i)→ 13Cα(i) transfer, 2TNC, during which the 15N magnetization is further modulated by 1JNCδ coupling interaction in prolines.
Figure 4 compares 3D Hα-detected with the new 4D spectra: problems associated with multifold overlap and ambiguities in choosing the right sequential connection when using 3D spectra can be surpassed, and the assignment procedure expedited by extending frequency labeling to Cα.
With the help of these Hα-detected 4D experiments, 76% of the α correlations of were successfully assigned (Suppl. Fig S2). Considering that some N, C′ resonances are separated by less than 0.05 ppm in the CON spectrum, e.g. corresponding resonances within73/113KDAISE78/118 differ only by 0.03–0.04 ppm, all peaks were not expected to be resolved in spectra with spectral resolutions of 0.11 (15N) and 0.05 (13C) ppm. The Hα, Cα shifts were as ineffective in providing the needed dispersion, the smallest peak separations being comparable, e.g. the 76/116Ile alpha peaks differ by only 0.01 and 0.05 ppm in 1H and 13C, respectively, and those of 77/117Ser even less (Suppl. Fig. S1).
4D (HACA)CON(CA)NH and (HACA)N(CA)CONH experiments
Analogously to 4D Hα-detected experiments described above, the 4D HN-detected experiments (Fig. 5), with an isolated proline assignment enhancement, are based on their 3D counterparts (Hellman et al. 2014). Again, sampling of an additional 15N dimension can be implemented in without introducing sensitivity loss thanks to the gradient enhanced coherence order selective coherence transfer (COS-CT) (Kay et al. 1992; Schleucher et al. 1994). Magnetization transfer through (HACA)CON(CA)NH and (HACA)N(CA)CONH experiments are briefly described in Eqs. 4 and 5, respectively:
Like in the Hα-detected experiments (vide supra), the magnetization is first transferred from 1Hα to 13Cα spin (time point a), and further to either 13C′(i–1) spin in (HACA)CON(CA)NH (density operator Cαz(i–1)C′y(i–1)) or selectively to 15N(i) spin in (HACA)N(CA)CONH (density operator Cαz(i)Ny(i)) at time point b. This is followed by the frequency labeling of 13C′(i–1) and 15N(i) chemical shifts during t1 in (HACA)CON(CA)NH and (HACA)N(CA)CONH experiments, respectively. Next, the desired magnetization is transferred to the sequential 15N spin or intraresidual 13C′ spin, described by the density operators Cαz(i–1)C′z(i–1)Ny(i) and Cαz(i)C′y(i)Nz(i + 1) in (HACA)CON(CA)NH and (HACA)N(CA)CONH, respectively (time point c). Frequency labeling of 15N(i) and 13C′(i) chemical shift takes place in t2. The suppression of sequential 15N pathway in (HACA)N(CA)CONH is accomplished using the intraresidual filtering between time points b and c, and in (HACA)CON(CA)NH between time points c and d. Finally, the chemical shift of 15N(i–1) and 15N(i + 1) chemical shifts are recorded for Cαz(i–1)Ny(i–1) and C′y(i)Nz(i + 1) coherences in (HACA)CON(CA)NH and (HACA)N(CA)CONH between time points d–e.
Hence, the 4D (HACA)CON(CA)NH and (HACA)N(CA)CONH spectra exhibit correlations at the intersection of ωHN(i–1), ωN(i–1), ωC′(i–1), ωN(i) and ωHN(i+1), ωN(i+1), ωC′(i), ωN(i) frequencies, respectively. As the magnetization transfer cascade originates from the Hα spin, and the transfer route includes sampling of 15N frequencies of prolines as well, the experiments facilitate assignment of isolated proline residues (XP or PX dipeptide stretches, where P is a proline and X stands for any non-proline residue) together with other residues in IDPs with high sensitivity. Analogously to Hα-detected experiments, under identical conditions (vide supra), the coherence transfer efficiency for both prolines and non-prolines in the 4D (HACA)CON(CA)NH experiment reaches 0.19, if 2TC is set to 28 ms (and 0.15 with 2TC = 6.2 ms) and in the (HACA)N(CA)CONH experiment I ~ 0.20. Hence, both of these experiments are optimal also for the proline assignment in XPX moieties.
In the 1H, 15N HSQC only 41% of the residues displayed resolved peaks, whereas from the two 4D spectra, accurate amide 1H, 15N shifts were obtained for 85% of BilRI residues. Still overlapping peaks were found for residues 73Lys-80Met, 113Lys-120Met and 153Lys-154Ala in the 71/111/151EVKDAI/VSEKM80/120/160 stretches as well as for residues 103Asp-105Ala, 143Asp-145Ala in the middle of the 99/139KDAKDAAADKM109/149 stretches. Despite the overlap, with the help of the high peak resolution in the CON, it was possible to walk sequentially the whole amino acid sequence with the exception of the first three residues, which are not part of the native BilRI sequence. These residues are missing also from the 1H, 15N HSQC, likely due to fast chemical exchange of their amide proton with the solvent protons. Examples of the resolving power of the additional 1H, 15N HSQC dimension are presented in Fig. 6 and Suppl. Figs. S3, S4. The sequential walk over a proline residue is depicted in Suppl. Fig. S5.
It is interesting to note that throughout the identical stretches 71/111EVKDAIVSEKMDAM83/123 and 99/139KDAKDAAADKM109/149 the corresponding peaks are resolved in the CON spectrum. Naturally, the chemical shift differences become small in the middle of the repeats, ~ 0.03–0.04 ppm for both C′ and NH, but the peaks remain, however, distinct. 76/116Ile Cα-Hα is resolved into separate peaks in a high-resolution CT 1H, 13C-HSQC spectrum (t1 acquisition time 51 ms) as well. To have a different chemical shift, the corresponding atoms in the stretches should experience a mutually different structural environment. Future studies will uncover whether this arises from nearest-neighbor effects being effective over five residues or from distinct long-range interactions within the protein.
During the past several years, several different NMR experiments and assignment schemes have been developed for studying IDPs. Based on the detected spin, these can be categorized to three different classes i.e. HN-, 13C′- and Hα-detection approaches (for review, see e.g., Brutscher et al. 2015). The HN-detected experiments offer the highest sensitivity under acidic conditions and can be combined with the BEST and TROSY implementations (Solyom et al. 2013; Brutscher et al. 2015). However, they show limited performance under alkali conditions and/or with IDPs having high proline content, which can be partially compensated using an Hα-start, HN-detected approach as shown here and also previously demonstrated (Mäntylahti et al. 2009; Hellman et al. 2014; Yoshimura et al. 2015). For instance, Yoshimura et al. (2015) proposed 13C′-13C′ TOCSY transfer in HNCOCONH -type experiments which show connectivities for i, i ± 1, i ± 2 residues i.e. enabling connection of i and i ± 2 residues over a single proline at i ± 1 position. The (HACA)CON(CA)NH and (HACA)N(CA)CONH experiments proposed here link the residues flanking a single proline through its 15N chemical shift.
Unlike HN-detected experiments, the 13C-detection is almost non-susceptible to amide proton exchange with water at high pH. The 13C-detection based experiments for the assignment of IDPs generally apply the ‘CON′ strategy for connecting the neighboring residues in low-complexity regions of IDPs, which is also suitable for the assignment of prolines (Pantoja-Uceda and Santoro 2014; Sahu et al. 2014; Brutscher et al. 2015; Chaves-Arquero et al. 2018). Theoretical coherence transfer efficiency in the 13C-detected experiment, hacaCONcaNCO (Pantoja-Uceda et al. 2014) attains 0.19, which is comparable to the sensitivity of the (HACA)CON(CA)NH experiment proposed here. However, given that γH/ γC equals 4 and the attainable sensitivity has γ3/2 dependence on the detected spin, the 13C-detection results in an inherent sensitivity loss by a factor of 8 with respect to the 1H-detection. This can partially be redeemed using a 13C-detection optimized probehead and 13C′-detection, which offers higher resolution in the direct detection dimension due to absence of homonuclear couplings. If such a probehead with an inner coil for 13C is not available, this sets limit to the feasible sample concentration (> 0.3–0.5 mM) which might become an issue with some IDPs. On the other hand, homonuclear couling between HN and Hα can be removed in 1H-detected experiments using the homonuclear BASH decoupling scheme (Ying et al. 2014).
Finally, the Hα-detected experiments offer higher sensitivity with respect to the 13C-detection, enable assignment of consecutive prolines and are not prone to linebroadening due to chemical exchange with the solvent (Mäntylahti et al. 2010, 2011). However, given that Hα resonances may partially be underneath the water signal unless sample is prepared in 99.99% D2O, all experiments proposed here employ the sensitivity-enhanced, echo/antiecho gradient selection in conjunction with the water flip back approach. This enabled us to carry out all the measurements in 95% H2O and accomplish a nearly complete assignment of Hα resonances of the 165-residue BilRI. When working with more dilute samples (< 0.25 mM), dissolving protein into D2O might be advantageous.
In all, with the proposed suite of 4D experiments, a complete assignment of backbone HN, NH, C′ chemical shifts was obtained for all but the three N-terminal residues, which are not part of the BilRI native sequence. Hα, Cα and Cβ chemical shifts were obtained for 87, 76, and 66% of the residues, respectively. These experiments offer alternative approach for the assignment of IDPs. Hence, they should not be considered superior per se to the existing methods, but as demonstrated here, they have features that may facilitate accomplishing the assignment of challenging IDPs such as BilRI.
In this paper, we have presented a suite of Hα-detected and Hα-start, HN-detected 4D experiments that by exploiting chemical shift dispersion brought by an additional Cα or N dimension, facilitate the unambiguous backbone resonance assignment of IDPs in comparison to their established 3D counterparts. The Hα-detected experiments provide versatile strategy for the assignment of proline-rich amino acid sequences and/or proteins at alkali pH, prone to fast chemical exchange with the solvent. The proposed 4D Hα-detected experiments provide information with the most vital chemical shifts i.e. Hα, 13Cα, and 13C′ for conformational restraining in IDPs. The Hα-start, HN-detected (HACA)CON(CA)NH and (HACA)N(CA)CONH experiments offer an alternative assignment protocol for IDPs, by providing connectivities over three sequential residues with the HN-detection that allows for connecting single proline-containing segments of the amino acid sequence. The feasibility of the proposed experiments was experimentally verified on with BilRI, a 165-residue protein, containing three highly similar 40-residue repeats and 12 K-D-A triplet sequences, which represents an extremely challenging case of resonance assignment of IDPs.
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Tossavainen, H., Salovaara, S., Hellman, M. et al. Dispersion from Cα or NH: 4D experiments for backbone resonance assignment of intrinsically disordered proteins. J Biomol NMR (2020). https://doi.org/10.1007/s10858-020-00299-w
- Aggregatibacter actinomycetemcomitans
- Resonance assignment
- Intrinsically disordered protein