High-Resolution In Situ NMR Spectroscopy of Bacterial Envelope Proteins in Outer Membrane Vesicles

The cell envelope of Gram-negative bacteria is an elaborate cellular environment, consisting of two lipid membranes separated by the aqueous periplasm. So far, efforts to mimic this environment under laboratory conditions have been limited by the complexity of the asymmetric bacterial outer membrane. To evade this impasse, we recently established a method to modify the protein composition of bacterial outer membrane vesicles (OMVs) released from Escherichia coli as a platform for biophysical studies of outer membrane proteins in their native membrane environment. Here, we apply protein-enriched OMVs to characterize the structure of three envelope proteins from E. coli using nuclear magnetic resonance (NMR) spectroscopy and expand the methodology to soluble periplasmic proteins. We obtain high-resolution in situ NMR spectra of the transmembrane protein OmpA as well as the periplasmic proteins CpxP and MalE. We find that our approach facilitates structural investigations of membrane-attached protein domains and is especially suited for soluble proteins within their native periplasmic environment. Thereby, the use of OMVs in solution NMR methods allows in situ analysis of the structure and dynamics of proteins twice the size compared to the current in-cell NMR methodology. We therefore expect our work to pave the way for more complex NMR studies of bacterial envelope proteins in the native environment of OMVs in the future.

T he structure, the conformation, and, consequently, the functional state of proteins are directly influenced by the surrounding environment. 1,2 Structural biology typically demands proteins be extracted from their natural cellular environment and studied under highly specialized conditions. 3,4 However, lately efforts to study proteins in situ using biophysical methods such as cryo-electron tomography and incell NMR spectroscopy are becoming more common. 5,6 One particularly complex cellular environment, which so far has evaded such efforts, is the cell envelope of Gram-negative bacteria, formed by two distinct membranes enclosing the periplasm, which contains a thin peptidoglycan wall. Despite more than one-third of the bacterial genome encoding envelope proteins, the envelope accounts only for 5−10% of the cellular volume. 7,8 This low volume ratio makes it complicated to study envelope proteins by established in situ methods (such as in-cell NMR spectroscopy), because envelope proteins are outnumbered by cytosolic proteins. On the contrary, the complexity of asymmetric bacterial outer membranes (the inner leaflet of which contains phospholipids, whereas the outer leaflet is formed exclusively by lipopolysaccharide) makes it impossible to mimic this unique environment to characterize envelope components in isolation by biophysical methods.
To overcome these limitations, we recently developed a new platform to study outer membrane proteins within their native membrane environment using protein-enriched outer membrane vesicles (OMVs). 9 These vesicles share the native membrane composition with the bacterial outer membrane they naturally bud from and carry periplasmic content in their lumen. OMVs can be purified from bacterial growth media in a nondestructive manner, providing an isolated cell envelope microenvironment. 10 Via overexpression of selected outer membrane proteins in Escherichia coli depletion strain BL21(DE3)omp8, 11 the protein composition of OMVs can be modified to contain a protein of choice at high density and purity. 9 In a pioneering study using atomic force microscopy (AFM), we demonstrated that proteins enriched in this way persisted in the membrane of OMVs in their native conformation. 9 However, because AFM can only provide low-resolution structural information, we here set out to elucidate the applicability of our OMV-based approach to obtain high-resolution structural information about envelope proteins under native conditions using NMR spectroscopy.
To this end, we prepared OMVs from BL21(DE3)omp8 enriched in the major outer membrane protein OmpA from E. coli, which anchors the outer membrane to the underlying peptidoglycan layer. 12 OmpA has a two-domain architecture containing an N-terminal transmembrane domain and a Cterminal soluble globular domain facilitating the interaction with the peptidoglycan. Especially the N-terminal transmembrane domain, which forms an eight-stranded β-barrel, has been extensively structurally characterized. 13−15 Due to its two-domain architecture, OmpA makes an ideal target to test our approach on the integral membrane part as well as the soluble domain. To facilitate efficient targeting of OmpA to OMVs, we inserted two-point mutations, D241A and R256A, which inhibit peptidoglycan binding 12,15 and result in greater enrichment of OmpA in OMVs ( Figure S1A). Moreover, to obtain OmpA-enriched OMVs uniformly labeled with stable isotopes ( 2 H and 15 N) to perform solution-state NMR experiments, culture conditions were optimized for growth in D 2 O-based M9 minimal medium (see the Experimental Section in the Supporting Information). Following isolation ( Figure 1A−C), we recorded NMR spectra of OmpA-enriched OMVs. While the resulting spectra showed several resonances ( Figure 1D), their 1 H chemical shifts were exclusively located around 8 ppm, corresponding to unstructured and flexible regions such as loops. We hypothesized that the size of OMVs and the resulting slow molecular tumbling of embedded proteins limit the spectral quality in these experiments. To optimize the size distribution of OMVs for NMR, OMVs were passed through a 50 nm liposome extruder, decreasing their diameter from 50−250 to ∼50 nm ( Figure 1E,F). Remeasuring the sample after extrusion resulted in substantially improved spectral quality, and multiple resonances corresponding to folded secondary structure elements could be detected ( Figure  1G). Comparison to reference spectra of OmpA in solution shows that these resonances almost exclusively correspond to the C-terminal soluble domain as well as flexible loops, whereas the N-terminal transmembrane domain remains largely undetected ( Figure S2). The latter can be explained not only by slower molecular tumbling rates of the transmembrane domain, compared to those of the soluble Cterminal domain, but also by the lack of back-exchange of amide protons within the membrane-embedded regions of OmpA, due to the expression in D 2 O-based media. The observation of the membrane-embedded domain of OmpA or other integral membrane proteins within OMVs might therefore be more achievable by solid-state NMR approaches developed for integral membrane proteins and in-cell NMR. 16,17 While this finding limits the prospect of studying transmembrane domains of outer membrane proteins in OMVs using solution NMR, it does open a unique opportunity to study soluble periplasmic proteins, given OMVs contain periplasmic proteins in a quasi-cellular context. Because the resonances that are visible in the spectrum of OmpA-enriched OMVs originated primarily from its periplasmic domain, we substituted BL21(DE3)omp8 with BL21(DE3)ΔompA, 18 to obtain OMVs containing all major porins except OmpA. The latter eliminates possible background signals originating from OmpA-CTD and results in an increased level of vesiculation compared to that of the parental BL21 strain. 18 To test the possibility of studying periplasmic proteins, we prepared OMVs luminally enriched in CpxP ( Figure S1B). CpxP is a soluble protein involved in envelope stress sensing via the CpxAR two-component system with a size comparable to that of OmpA-CTD (∼17 kDa). In contrast to the spectrum of OmpA, the spectrum of OMVs containing CpxP featured a set of well-resolved resonances ( Figure 2) and did not require prior extrusion of the OMVs. For comparison, we recorded and assigned a reference spectrum of purified CpxP, which showed a high degree of similarity to that of CpxP-enriched OMVs ( Figure S3). Comparison to spectra of OMVs prepared in the absence of protein enrichment showed that, with the exception of five strong background signals, the observed resonances could indeed be directly attributed to CpxP ( Figure  S4A−C). In a next step, we assessed the influence of    Figure 2B and Figure S3), indicating a mostly α-helical structure of purified CpxP in solution and, consequently, inside of OMVs. To assess the protein concentration inside OMVs and to test whether it resembles the concentration in the natural periplasmic environment, we used an approach adapted from in-cell NMR spectroscopy. 21 Figure  S5A,B). We then estimated the total vesicle volume from the turbidity of the NMR sample by first determining the vesicle radius from the slope of logarithmized optical density spectra ( Figure S5C,D) followed by determining the corresponding number concentration from the optical density. 24−26 This resulted in an estimated CpxP concentration of ∼1.7 mM inside OMVs and is in agreement with values determined for periplasmic α-synuclein in previous studies. 27 Encouraged by the high quality of the CpxP spectra, we applied the methodology to a much larger system, the 40 kDa periplasmic maltose binding protein MalE (MBP), which is frequently used as a reference standard for NMR measurements of large proteins. 28−30 We thus prepared OMVs containing high levels of MBP using BL21(DE3)ΔompA, resulting in NMR spectra of exceptional quality ( Figure 3A). Compared to spectra of purified MBP, we could observe ∼50% of all resonances. The lack of completeness can be explained by insufficient back-exchange of amide protons within the solventinaccessible folded core of the protein, compared to in vitro samples that were prepared with back-exchange of amide protons by chemical denaturation. Indeed, mapping the positions of the detected resonances shows that these are mostly located on the surface of MBP ( Figure 3B). Comparison to reference spectra moreover allowed us to observe that intra-OMV MBP persisted in its ligand-bound holo state.
We next set out to compare OMV NMR results to in-cell NMR results, which so far has been applied successfully only for small intracellular proteins of ≤15−20 kDa. 31,32 To achieve direct comparability, we performed sequential experiments from in-cell to in situ to purified and refolded MBP subsequently on the same sample preparation (Figures S1 and S6). To this end, we first expressed periplasmic MBP in BL21(DE3)ΔompA and removed a culture sample to collect an in-cell NMR spectrum, just before purifying OMVs from the culture supernatant ( Figure 3C). We subsequently recorded a spectrum of the OMVs prepared from the same culture. Unlike the spectrum of MBP in OMVs, the in-cell spectrum shows only a basic resemblance to reference spectra of MBP; thus, we could identify only ∼20% of the residues of MBP ( Figure 3D). For direct comparison to spectra of isolated MBP, we dissolved the OMVs by adding Triton X-100 and purified the released MBP to record a spectrum of the purified protein. The latter closely resembles that recorded for MBP in OMVs ( Figure  S6). We next unfolded and refolded MBP to facilitate the complete back-exchange of backbone amide protons as well as the eventual release of ligands bound to MBP. Recording a spectrum following the procedure not only increased the number of detected resonances from ∼50% to >80% but also confirmed that the conformation of MBP had changed to its apo state ( Figure S6). Ultimately, we added maltose and recorded a final spectrum ( Figure 3E). With the exception of  Biochemistry pubs.acs.org/biochemistry Communication the additional resonances attained through the amide proton back-exchange, the spectrum closely resembles the original in-OMV spectrum as well as reference spectra and shows that MBP reverted to the holo state ( Figure 3F).
To relate the conditions of in-OMV NMR experiments to those of in-cell NMR experiments, we repeated the signal intensity-based concentration estimation with MBP in OMVs and in-cell MBP, resulting in sample concentrations of 539 and 165 μM, respectively ( Figure S7). Analysis of the turbidity of the OMV sample resulted in a luminal MBP concentration of ∼6.2 mM ( Figure S7). In comparison, the concentration of periplasmic MBP in the in-cell NMR sample was estimated to be ∼7.4 mM ( Figure S8). While these estimated concentrations appear to be relatively high, they merely correspond to an ∼7-fold increase in the level of overexpressed MBP over native periplasmic MBP levels of ∼1 mM 33 and are within the limits of a suggested total periplasmic protein concentration exceeding 300 mg mL −1 . 27 Moreover, the high enrichment level of MBP in OMVs is reflected in the signal intensity, which matched the level of the five strong background signals otherwise observed in OMVs ( Figure S7E,F). Notably, the MBP concentration was in a similar range in both samples, suggesting that the luminal environment of OMVs closely resembles the periplasmic space of the parental bacterial cells. To further elucidate the cause of the substantially increased quality of MBD spectra in OMVs compared to in-cell, we analyzed the line width of a subset of resonances ( Figure S7G). Whereas we do not see any effects in 15 N line widths, we observe an average 1 H line width of 29 ± 7 Hz for the in-cell sample compared to around 19 ± 5 Hz for all other conditions, indicating a slightly more crowded environment under in-cell conditions, which can be explained by the slower lateral diffusion due the presence of the peptidoglycan layer, 34 or the known effect of magnetic inhomogeneity of dense cell samples. 35 Together, our experiments clearly demonstrate the potential of protein-enriched OMVs as proxies for in situ studies of bacterial envelope proteins. The potential of the outlined approach thereby seems to be limited for integral outer membrane proteins, for which we could only partially resolve the soluble domain of OmpA. Unlike the case of OMVs enriched in periplasmic proteins, NMR experiments with OmpA required the OMVs to be extruded, which might entail perturbation of membrane features such as asymmetry and curvature as well as leakage of luminal proteins. In contrast, the prospect of studying soluble periplasmic proteins within their quasi-native environment is intriguing. NMR experiments with OMVs enriched in CpxP as well as MBP resulted in highquality spectra, which allowed us to directly assess the conformation of these proteins within their cellular context. Moreover, using OMVs resulted in a vast increase in spectral quality and allowed proteins of more than twice the size to be studied compared to what has been achieved using conventional in-cell NMR experiments thus far. Our experiments therefore pave the way for more complex NMR studies of bacterial envelope proteins in the native environment of OMVs in the future. The usage of OMVs will be of particular advantage for proteins, which depend on specific features of the complex periplasmic environment, for example, proteins requiring the oxidative formation of disulfide bonds 36,37 or proteins affected by macromolecular crowding. 38 The ability to perform structural studies in situ may also improve our understanding of the mechanistic details of proteins, which occur naturally enriched in OMVs, such as virulence factors and proteins involved in quorum sensing. 39 ■ ASSOCIATED CONTENT