Many biopharmaceutical products exhibit extensive structural micro-heterogeneity due to an array of co-occurring post-translational modifications. These modifications often effect the functionality of the product and therefore need to be characterized in detail. Here, we present an integrative approach, combining two advanced mass spectrometry-based methods, high-resolution native mass spectrometry and middle-down proteomics, to analyse this micro-heterogeneity. Taking human erythropoietin and the human plasma properdin as model systems, we demonstrate that this strategy bridges the gap between peptide- and protein-based mass spectrometry platforms, providing the most complete profiling of glycoproteins. Integration of the two methods enabled the discovery of three undescribed C-glycosylation sites on properdin, and revealed in addition unexpected heterogeneity in occupancies of C-mannosylation. Furthermore, using various sources of erythropoietin we define and demonstrate the usage of a biosimilarity score to quantitatively assess structural similarity, which would also be beneficial for profiling other therapeutic proteins and even plasma protein biomarkers.
Most human proteins are decorated by a plethora of post-translational modifications (PTMs) regulating their structure, function and interactions. Protein PTMs, such as phosphorylation, acetylation, ubiquitination, and glycosylation, have all been shown to regulate a wide range of biological processes. Protein glycosylation represents likely the most heterogeneous PTM owing to the plethora of co-occurring carbohydrate structures. Protein glycosylation regulates in particular signalling, cell–cell communication and regulation of host–pathogen interactions1,2,3, providing valuable targets for inhibition of infection4.
Over the last decade bottom-up mass spectrometry (MS) based proteomics has emerged as a powerful technique for protein PTM identifications, whereby proteins are first enzymatically digested and thereafter PTMs are identified at the peptide level5,6,7. In bottom-up MS approaches, tandem MS (MS2) fragmentation can be effectively performed on peptides, enabling the characterization of PTM site-localizations and the structure of modifications8. A downside of bottom-up approaches, however, is that the peptides analysed contain mostly single PTMs hampering the investigation of the whole-protein picture. Especially in recent years, with the novel strategies of glycopeptide enrichment and hybrid MS fragmentation, bottom-up MS is widely applied to glycopeptide characterization9,10,11,12,13. Since glycopeptides are on average much larger than their non-modified counterparts (arbitrarily 3<Mw <10 kDa), which requires non-standard approaches in chromatography and fragmentation, glycopeptide analysis may be considered an explicit form of middle-down proteomics14,15,16.
The co-occurrence of PTMs can also be investigated by MS at the intact protein level17,18. With the advent of high mass accuracy and resolving power of MS technologies, it has now become possible to detect and baseline resolve different proteoforms directly from intact proteins under pseudo-physiological native conditions, using a modified Orbitrap mass analyzer with an extended mass range19,20,21,22,23,24,25. This approach has enabled the PTM analysis of the intact ovalbumin to an unprecedented depth, where 59 different proteoforms were detected, identified and quantified from a single-shot experiment26. It is of great advantage that native MS provides a direct view on the relative abundance and overall PTM composition of different co-appearing proteoforms that are distinguishable in mass27,28. Yet, the detailed information of the protein PTMs, such as site specificity, structure and stoichiometry on each modification site, cannot be directly extracted from the native MS data. The situation becomes more complicated when the protein of interest contains multiple PTM sites and types, especially when heterogeneous glycosylation is involved as well.
Here we present an integrative workflow to obtain a comprehensive picture of PTMs on proteins by integrating native MS and middle-down proteomic strategies (Fig. 1). As a proof of concept, we selected two structurally highly heterogeneous proteins, recombinant therapeutic human erythropoietin (rhEPO) and properdin, which were directly purified from human blood serum. Both proteins contain high and diverse amount of PTMs, demonstrating the applicability of our integrated approach in some of the most challenging scenarios. For both the proteins, we detected, identified and quantified hundreds of proteoforms with distinguishable masses at the intact protein level and also assessed detailed information of each PTM site by middle-down proteomic approaches. Furthermore, we performed in silico construction to simulate a pseudo native MS spectrum combining the site-specific PTM data obtained by the middle-down strategy. The resulting constructed intact-protein representation allowed us to directly compare the result from middle-down experiments with the native MS data. This led to the unambiguous discovery of three previously unreported C-glycosylation sites on properdin. Furthermore, our study reports for the first time an extensive heterogeneity in occupancy of the C-mannosylation sites in the six thrombospondin repeat (TSR) domains on this protein.
We also characterized the structural heterogeneity of rhEPO therapeutics obtained from different manufacturers and sources. These rhEPO therapeutics often contain identical protein backbone sequence, albeit decorated with differential PTMs due to different conditions in their production. Technically, it is very important, yet challenging, to quantify the similarity of these therapeutics in a robust and reproducible way29,30,31. We here introduce a biosimilarity score to describe the level of structural similarity of three rhEPO therapeutics, demonstrating its usage in direct assessment of the similarity of therapeutic glycoproteins. This strategy is well applicable to other protein therapeutics, such as antibodies, thus providing a wide application range of the presented concept.
Proteoform profiling of intact rhEPO by native MS analysis
The molecular heterogeneity of rhEPO is mainly caused by O-glycosylation at S126 and N-glycosylation at three different sites; N24, N38 and N83 (Fig. 2a). When recording the full proteoform profile of intact rhEPO by high-resolution native MS, over 230 peaks were baseline resolved, and the overall PTM composition was assigned with satisfying mass accuracy (Fig. 2b and Supplementary Table 1). The rhEPO backbone sequence has a theoretical mass of 18,235.99 Da, and the protein masses (that is, the total molecular weight of the backbone and PTMs) measured by native MS possessing a range of 26,000 to 33,000 Da (Supplementary Table 1). This large mass difference demonstrates that about 40% of the mass is originated from glycosylation. The most abundant peak (measured mass: 29,888.12 Da, PTM composition: Hex22HexNAc19Fuc3Sia13) in the native MS spectrum likely comprises multiple proteoforms exhibiting mass alike, owing to either the combinatorial arrangement of multiple PTMs on different sites, adding up to exactly the same total mass, and/or different PTM compositions that are very close in mass. The high S/N ratio (∼11,000) allows us also to distinguish and identify lower abundant PTMs, such as the minor modifications of sialic acid by O-acetylation and –CH3 to –CH2OH replacement, as illustrated in Fig. 2b.
Next, we also measured the sialidase-treated rhEPO by native MS approach. The enzymatic removal of sialic acid residues resulted in a pronounced simplification of the structural variability of rhEPO proteoforms (Fig. 2c), implying that the heterogeneity of rhEPO is mainly due to the extensive decoration with variable amounts of sialic acids. After the enzymatic treatment, the most abundant m/z peak shifted to 26,102.55 Da (measured mass), which exactly corresponds to a loss of 13 sialic acids. This provides further evidence to our initial composition assignment (Hex22HexNAc19Fuc3Sia13) in the non-treated rhEPO sample.
Site-specific PTM analysis of rhEPO by middle-down proteomics
To characterize each modification site in detail, we digested rhEPO with the aim to separate all PTM sites into individual (glyco)peptides with suitable length by middle-down proteomics. Following careful optimization, we selected trypsin to assess the N83 and S126 glycosylation sites, and Glu-C to examine the N24 and N38 glycosylation sites. In the liquid chromatography/mass spectrometry (LC/MS) experiment, the peptide mixture was subjected to higher-energy collisional dissociation (HCD) LC/MS2 analysis. To obtain extensive fragment ions of both glycan and peptide moieties of glycopeptides, additional collision-induced dissociation (CID) and electron-transfer and higher-energy collision dissociation (EThcD) fragmentation were applied when monosaccharides and/or disaccharides were detected in the HCD spectrum (‘Methods’ section). CID spectra were used to sequence the glycan branches while EThcD spectra were used to improve the sequence coverage of the peptide moiety. We also assessed the relative abundances of the differentially modified isoforms in a site-specific manner, based on the extracted ion chromatograms (XICs) of the identified peptides (‘Methods’ section).
As a result, we identified and relatively quantified (i) 10 glycoforms on N24, (ii) nine glycoforms on N38, (iii) eight glycoforms on N83 and (iv) two glycoforms on S126 (Fig. 3). For the O-glycosylation site on S126, we also detected the non-modified peptide. Our data revealed that each N-glycosylation site of rhEPO was modified uniquely in terms of both the numbers and relative abundances of differentially modified glycoforms. Similar to the native MS spectrum, we also observed additional modifications of NeuAc in our proteomic experiments, evidenced by multiple additional peaks (+16 Da, +42 Da or the combination of the two) next to the main glycoforms. It is known that NeuAc can be substituted with NeuGc by −CH3 to −CH2OH replacement (+16 Da; ref. 32). In addition, both NeuAc and NeuGc can be modified with O-acetylation (+42 Da; ref. 33). Interestingly, we noticed that the NeuAc modification patterns are distinctive at different glycosylation sites. For instance, we detected peaks generated from both NeuGc and O-acetylation at N38 and N83; however only from NeuGc at N24. We do not have a clear biological explanation, but these observed differences could result from dissimilarities of synthetic pathways involved and/or distinct solvent accessibilities of each glycosylation site.
Integrating native and middle-down MS for PTM profiling
As described, we applied two complementary approaches to characterize the complex PTM profile of rhEPO. Next, we set out to further develop an integrative strategy to combine the information from both approaches. Briefly, given the masses and relative abundances of all PTM isoforms at each site, we constructed a native protein spectrum in silico based on a probability model, assuming all modifications are independent events (see ‘Methods’ section for detailed description). This spectrum is a representation of all possible proteoforms that may exist in the sample, therefore should comprise all proteoforms detected in the native MS experiment. Positional isomers, which exhibit the same total mass, cannot be distinguished in this scenario. In this regard, we were able to compare the data from the two independent experiments and further assess the integrity of the middle-down PTM assignments.
Using the middle-down data from all PTM sites of rhEPO, we successfully constructed an intact protein spectrum that largely resembled the experimental native MS spectrum (Fig. 4a). The Pearson correlation coefficient of the two spectra was 0.86, indicating a high similarity of the two independent approaches. On the basis of the middle-down data, we further simulated a spectrum wherein all the sialic acids were removed, and compared it with the native MS data acquired from rhEPO sample treated by sialidase. In this spectrum pair (Fig. 4b), the Pearson correlation coefficient increased from 0.86 to 0.94, and nearly all proteoforms in the native MS spectrum can be annotated to the corresponding peaks in the constructed spectrum. It is known that in bottom-up and middle-down analysis, glycopeptides may easily lose their labile sialic acid moiety during sample preparation and ionization34,35. At the intact protein level, few studies are available regarding to this question. Rosati et al.21 analysed four IgG4 hingeless mutants that exhibiting complex glycosylation including di-sialylation and tri-sialylation, and they observed that after removing sialylation, the charge state envelopes were not shifted compared with the sialylated samples. Therefore, under the conditions of native MS analysis, these labile groups remain attached to the protein, and also at the intact protein level the negatively charged sialic acid groups introduce less ionization bias21. This is likely a cause for the lower correlation observed on the unprocessed rhEPO, when compared with the sialidase-treated sample.
Unanticipated PTM features in the plasma protein properdin
We next studied the plasma protein properdin, also named as Factor P36,37, representing one class of important glycoproteins. Properdin is a member of the complement protein family and plays a critical role during complement activation38. It has been suggested that the PTM profile of properdin derived from blood serum and neutrophil/mast cell may differ from each other, resulting in different biological outcomes39. The high and diverse amount of PTM sites (over 20 potentially modified sites), including N- and O- glycosylation, as well as C-mannosylation, make properdin an interesting but challenging target for analysis (Fig. 5a). Specifically, it contains 6 thrombospondin repeat domains (TSR1-TSR6), known to be substrates for C-mannosylation, an unusual type of protein glycosylation whose exact function are yet not well understood40. We firstly performed native MS and middle-down proteomics to comprehensively characterize its PTM heterogeneity. In the native MS spectrum, we detected more than 30 peaks, and assigned the overall PTM composition for the significant ones (Fig. 5b). Next, we treated properdin with PNGase F, to remove the N-glycans. The resulted spectrum confirmed that the heterogeneity of properdin originates mainly from C-mannosylation, not N-glycosylation (Supplementary Fig. 1). Although properdin contains over 20 PTM sites, we were able to assign most of the peaks in the high resolution native MS spectrum. The extent of N-glycosylation, which is usually the main cause of glycoprotein heterogeneity, was found to be rather homogeneous on properdin. We demonstrated that our approach can analyse highly heterogeneous proteins and therefore its application for other plasma proteins may provide new insights on their PTM composition in unprecedented details and confidence comparing with currently used strategies. In the middle-down experiments, we identified and relatively quantified a variety of site-specific PTM isoforms originating from a staggering number of 17 C-mannosylation sites, four O-glycosylation sites and one N-glycosylation site (Fig. 5a). Three out of 17 identified C-mannosylation sites (W80, W202 and W318) have not been previously reported. The MS2 spectra of the three peptides associated with the new sites provide a good confidence of the type of modification at these sites (Supplementary Fig. 2).
To further validate the three newly discovered C-mannosylation sites and the integrity of our middle-down PTM identification, we examined the middle-down data using the integrative approach described above. To this end, we constructed the native MS spectrum of properdin with or without the three newly discovered C-mannosylation sites. We clearly observed that, excluding the three novel C-mannosylation sites, several peaks were absent in the constructed spectra missed peaks in comparison with the native MS spectrum. The mass difference of 162 Da between the adjacent peaks at m/z range 3,860–3,900 implied the presence of three additional C-mannosylation sites at the intact protein level (Fig. 5d). After incorporating the three C-mannosylation sites in the constructed spectrum, as shown in Fig. 5e, the spectra pair looked more similar and also provided a higher Pearson correlation coefficient (0.95).
In contrast to previously reported data41, where all the C-mannosylation sites were suggested to be fully occupied, our data reveal the existence of high heterogeneity in site occupancy in five out of the six TSR regions. On TSR1, TSR2, TSR3, TSR5 and TSR6, the second tryptophan in the recognition motif W-X-X-W-X-X-W was found to be fully C-mannosylated, while the first and the third tryptophan were modified only partially with different level of occupancy. A more detailed description on C-mannosylation heterogeneity in the TSR structures of properdin is described in Fig. 5c and Supplementary Note 1. To our knowledge, this is by far the most thorough description of the structural heterogeneity occurring in plasma-derived properdin.
Assessing biosimilarity in rhEPO samples
The approval of a biosimilar product requires a thorough characterization, which requires the compatibility with the reference product in quality, safety and efficacy. Protein-based biosimilars often have the same backbone sequence, but may embed heterogeneity in their PTM profiles, which challenges current similarity analysis. This heterogeneity results from differences in production cell lines, culture conditions and production methods. To address the need for distinguishing biosimilar products analytically, we next demonstrate how high-resolution native mass spectrometry and our Pearson correlation-based algorithm can be used to define spectra similarity between different rhEPO products, taking three available rhEPO samples as model systems; rhEPO biological reference (BRP), epoetin beta and epoetin zeta (a biosimilar of epoetin alpha). Their respective native MS spectra are shown in Fig. 6a.
First, to assess the reproducibility of our native MS approach, we measured the correlations of technical replicates of each rhEPO sample. Our results showed all the spectral correlations were above 0.97, indicating a robust analytical reproducibility of our approach (Fig. 6c, measurement of duplicates are marked as beta and beta′, BRP and BRP′, zeta and zeta′). Next, we compared the samples from the different sources and observed clear differences in terms of the relative abundance of each m/z peak (Fig. 6a). The correlation between epoetin beta and epoetin zeta is relatively low (∼0.45), implying the distinct PTM profiles of these two rhEPO products. Notably, this observation is in agreement with a previous study that reported distinctive glycosylation patterns on epoetin alpha (a biosimilar of epoetin zeta) and beta42. The rhEPO BRP and epoetin beta were found to correlate better (∼0.75) than epoetin beta and zeta (∼0.45), so do rhEPO BRP and epoetin zeta (∼0.67). The observed order in these correlations were somewhat expected since rhEPO BRP contains a mixture of epoetin alpha and beta in equal amounts (w/w; ref. 43).
Next, we treated the three rhEPO samples with the enzyme sialidase. This resulted in an extensive reduction of the heterogeneity in the native MS spectra (Fig. 6b). Concomitantly, the correlation increased to 0.92 between desialylated epoetin beta and zeta, 0.94 between desialylated epoetin beta and rhEPO BRP, and 0.95 between desialylated epoetin zeta and rhEPO BRP (Fig. 6d). These results demonstrate that the PTM heterogeneity of rhEPO products is largely originating from the variability in the extent and occupancy of sialylation on the various glycan trees occurring in rhEPO.
We applied middle-down proteomics, native MS and an integrative strategy to comprehensively assess the PTM features of rhEPO and the plasma derived properdin. Using high-resolution native MS, we obtained a qualitative and quantitative view of all co-appearing proteoforms. By using a complementary middle-down proteomic approach, we in detail revealed PTM localizations, relative abundances and glycan structures in a site-specific manner. Beneficially, we were able to assess the reliability and integrity of our PTM assignments by a direct comparison of the data from both approaches, leading us to the discovery of three new C-mannosylation sites as well as the undescribed structural heterogeneity in site occupancy in properdin. This integrated comparison bridges the two MS platforms, adding a new layer towards the completeness and confidence of PTM assignments.
In current analytical workflows, the characterization of structural similarity between rhEPO products poses a great challenge, largely owing to the introduction of bias during sample preparation, analytical processes and the lack of resolving power. Here, we show that high-resolution native MS, which requires minimal sample preparation and analysis time, nicely addresses this challenge by providing a quantitative fingerprint of the intact protein. Particularly, native MS is extremely powerful at quantifying the distinct PTM patterns of glycoproteins with heavy sialylation. These monosaccharides are substantially important for the biological activities and the in vivo circulatory half-life of many biopharmaceutical products, such as rhEPO44,45, yet are very challenging for quantification because they introduce ionization bias to the sialylated glycopeptide and quite fragile during sample preparation.
The hereby presented high-resolution native MS analysis and biosimilarity scoring could also be applied to other glycoprotein biologics, such as therapeutic antibodies, which exhibit typically less heterogeneous PTM profiles compared with rhEPO. Of interest, in biotechnological applications, glycosylation of glycoproteins becomes more and more directed by perturbing specific glycosyltransferases in the host cell46,47,48. Such approaches lead to glycoproteins decorated by a plethora of varied PTMs. The effect of deletion of glycosyltransferases on the produced product could be efficiently monitored and characterized by the hereby-presented strategies.
The integrative approach offers a direct measurement of the molecular heterogeneity and can be in theory applied to any protein with PTM decoration. Plasma glycoproteins form some of the most relevant protein biomarker targets. Next to changes in abundance levels of such proteins, changes in PTM/glycosylation profiles may provide even stronger biomarker signatures49,50,51,52. The hereby-presented combined approach united high-resolution native mass spectrometry and middle-down proteomics for the structural analysis of glycoproteins and may, therefore, also find applicability in a variety of biotherapeutical as well as biotechnological applications.
The recombinant rhEPO BRP (presently batch 4.0) was acquired from EDQM (European Directorate for the Quality of Medicines). It is a 50:50 blending of epoetin alpha and epoetin beta53, supplied at 13,000 IU per vial. Epoetin beta was acquired from Roche and supplied at 30,000 IU per syringe. It is a recombinant form of erythropoietin marketed under the trade name NeoRecormon, produced by recombinant DNA technology using Chinese hamster ovary cells as expression system. Epoetin zeta (Retacrit, Hospira) is a biosimilar to the reference medicinal product Eprex (Epoetin alpha), produced in Chinese hamster ovary cells. The Uniprot code for rhEPO is P01588. Human blood plasma properdin (Uniprot code: P27918) was obtained from Complement Technology, Inc. (TX, USA). Urea, dithiothreitol (DTT) and iodoacetamide were purchased from Sigma-Aldrich (Steinheim, Germany). Formic acid (FA) was purchased from Merck (Darmstadt, Germany). Acetonitrile (ACN) was purchased from Biosolve (Valkenswaard, The Netherlands). Sequencing grade trypsin was obtained from Promega (Madison, WI, USA). Glu-C, Asp-N, PNGase F and Sialidase were obtained from Roche (IN, USA).
Sample preparation for native MS
Unprocessed protein solutions (containing 25–30 μg of the protein) were buffer exchanged into 150 mM aqueous ammonium acetate (pH 7.5) by ultrafiltration (vivaspin500, Sartorius Stedim Biotech, Germany) using a 5 kDa cut-off filter. Protein concentration was measured by ultraviolet absorbance at 280 nm and adjusted to 2–3 μM before native MS analysis. Sialidase was used to remove sialic acid residues from rhEPO. PNGase F was used to cleave the N-glycans of rhEPO and properdin, four units of PNGase F with 25 μg of purified protein sample (concentrated ∼0.5 mg ml−1) were mixed and incubated at 37 °C overnight. All the samples were buffer exchanged to 150 mM ammonium acetate (pH 7.5) before native MS measurements. Typically 2 μl of the concentrated sample (2 μM) were directly infused into the mass spectrometer, and the leftover from the native MS measurement can be recovered and stored if needed.
Native MS analysis
Samples were analysed on a modified Exactive Plus Orbitrap instrument with extended mass range (Thermo Fisher Scientific, Bremen, Germany) using a standard m/z range of 500–10,000 Th. The voltage offsets on transport multi-poles and ion lenses were manually tuned to achieve optimal transmission of protein ions at elevated m/z. Nitrogen was used in the HCD cell at a gas pressure of 6–8 × 10−10 bar. MS parameters used: spray voltage 1.2–1.3 V, source fragmentation 30 V, source temperature 250 °C, collision energy 30 V and resolution (at m/z 200) 17,500. The instrument was mass calibrated using CsI clusters.
Native MS data analysis
The raw spectra were deconvoluted to zero-charge spectra using the Bayesian Protein Reconstruct tool from BioAnalyst ver. 1.1 (ABSciex). The mass range and m/z range were adjusted accordingly. Average masses were used for PTM calculation, including hexose/mannose/galactose (Hex/Man/Gal, 162.1424 Da), N-acetylhexosamine/N-acetylglucosamine (HexNAc/GlcNAc, 203.1950 Da), deoxyhexose (dHex, 146.1430 Da), N-acetylneuraminic acid (Neu5Ac, 291.2579 Da), N-glycolylneuraminic acid (Neu5Gc, 307.2573 Da), phosphorylation (Pho, 79.9799 Da), acetylation (Acetyl, 42.0373 Da) and –CH3 to –CH2OH replacement (Hydroxyl, 15.9994 Da).
Proteolytic digestion for middle-down proteomics
Proteins (rhEPO, and properdin) were reconstituted or buffer exchanged to PBS (phosphate-buffered saline, pH 7.4) and protein concentration was adjusted to 1 mg ml−1. Subsequently, the samples were reduced with 4 mM DTT at 56 °C for 30 min and alkylated with 8 mM iodoacetamide at room temperature for 30 min in the dark, whereafter 4 mM DTT was added again. rhEPO was digested with either trypsin at an enzyme-to-protein-ratio of 1:100 (w/w) or Glu-C at an enzyme-to-protein ratio of 1:75 (w/w) overnight at 37 °C. Properdin was digested for 4 h with either Glu-C or Asp-N at an enzyme to-protein-ratio of 1:75 (w/w) and further treated with trypsin (1:100; w/w) overnight at 37 °C. For glycopeptide analysis, we typically digested 3 μg of protein for digestion, and injected 1 pmol of the resulted peptide mixture on the columns.
After proteolytic digestion, all peptides (including glycopeptides) were separated and analysed using an ultra HPLC Proxeon EASY-nLC 1000 system (Thermo Fisher Scientific, Odense, Denmark) coupled online to an Orbitrap Fusion mass spectrometer (Thermo Fisher Scientific, Bremen, Germany). Reversed-phase separation was accomplished using a 100 μm inner diameter 2 cm trap column (in-housed packed with ReproSil-Pur C18-AQ, 3 μm; Dr Maisch GmbH, Ammerbuch-Entringen, Germany) coupled to a 50 μm inner diameter 50 cm analytical column (in-house packed with Poroshell 120 EC-C18, 2.7 μm; Agilent Technologies, Amstelveen, The Netherlands). Mobile-phase solvent A consisted of 0.1% FA in water, and mobile-phase solvent B consisted of 0.1% FA in ACN. The flow rate was set to 100 nl min−1. A 50 min gradient (7–30% solvent B within 31 min, 30–100% solvent B within 3 min, 100% solvent B for 5 min, 100–7% solvent B within 1 min and 7% solvent B for 10 min) was used. For rhEPO, MS2 HCD was performed with normalized collision energy of 35%. Product ion trigger was enabled to additionally trigger CID and EThcD MS2 acquisitions of the same precursor ion if glycan masses (HexNAc: 204.0867; HexNAc fragment: 138.0545; HexNAcHex: 366.1396) were observed. CID was performed with a normalized collision energy of 25% and EThcD was performed using calibrated charge dependent ETD parameters with an EThcD supplementary activation collision energy of 20%. This allowed additional fragmentation information of both the glycan and the peptide moieties of glycopeptides. For properdin, MS2 EThcD were acquired. HCD was performed with normalized collision energy of 15% and 35%, respectively. A supplementary activation energy of 20% was used for EThcD. All the spectral data were acquired in the Orbitrap Fusion mass analyzer. For the MS scans, the scan range was set from 375 to 2,500 m/z at a resolution of 60,000 and the AGC target was set to 1 × 106. For the MS2 scans, the resolution was set to 15,000; the AGC target was set to 1 × 105; the precursor isolation width was 1.6 Da and the maximum injection time was set to 300 ms. The CID normalized collision energy was 35% and the ETD AGC target was set to 1 × 105.
LC/MS data analysis
The raw data were analysed by Byonic software (Protein Metrics Inc.) using the following parameters: precursor ion mass tolerance, 10 p.p.m.; product ion mass tolerance, 20 p.p.m.; fixed modification, Cys carbamidomethyl; variable modification: Met oxidation, STY phosphorylation, and both N- and O- glycosylation from mammalian glycan databases; allowed number of mis-cleavages: 3. For searching of the peptides we used either rhEPO or properdin protein sequences. For site-specific relative quantification, the XICs were calculated using Skyline54. Each peptide that contains PTM sites was normalized individually so that the sum of all its proteoform areas was set at 100%. The glycan structure of each glyco-isoform was manually annotated on the basis of mass, MS2 fragmentation and confirmed as the most likely structure in literature8,32,33,55,56. Using MS2 fragmentation pattern, it is not possible to identify the linkage type of glycan units, such as α2–3 and α2–6 linked sialic acid, or Galβ1-4GlcNAc and Galβ1-3GlcNAc. Therefore, we did not include any linkage information in our reported glycan structures. All MS2 spectra provided fragments, which unambiguously confirmed identity of all modified peptides, type and composition of PTM.
Middle-down data construction of pseudo-native MS spectrum
We perform in silico data construction to simulate a native MS spectrum based on the masses and relative abundances of all site-specific PTM information derived from middle-down proteomics (The algorithm is made publicly available and supplemented at https://github.com/Yang0014/glycoNativeMS). The data construction is achieved on the basis of the following three elements: (1) the mass of the protein backbone retrieved from the protein sequence, (2) the masses of the PTMs on each modification sites as extracted from the middle-down data and (3) the relative abundances of site-specific PTMs extracted from LC chromatogram.
In detail, we first calculate the masses of all proteoforms based on all PTM identified from middle-down measurements. The mass of a proteoform M can be calculated as:
where Mpp is the mass of the polypeptide portion of a given protein, which is calculated using the backbone amino acid sequence corrected for disulfide bridges; n is the number of PTM sites. mij is the mass of the j-th modification at site i.
Second, we calculate the relative abundance P of a proteoform determined by its unique PTM combination, which is calculated by:
where Pij is the normalized relative abundance of the j-th modification at site i; n is the number of PTM sites.
where k is the number of possible PTM isoforms at site i (including unoccupied site); Aij is the abundance of j-th modification at site i, which is calculated based on the XIC.
To avoid artefacts possibly induced by spectra deconvolution, the constructed data are further processed to include a charge state envelope. In this regard, it can be directly compared with the unprocessed native MS spectra. The m/z spectrum is generated by converting protein masses (M) to m/z values (Q):
The native mass spectrum of a given protein often has a (limited) charge envelope ranging from [M+mH]m+ to [M+nH]n+, therefore we also simulate the constructed data with the same charge envelope. Ak is the relative abundance of k-th charge state Zk, m≤k≤n.
Assessing the similarities of native MS spectra
Native MS spectra (acquired in profile mode) are first pre-processed by binning data points into defined m/z ranges. Subsequently, the standard Pearson correlation is performed to score the similarity of two spectra.
An optimal bin width should be as small as possible to precisely reflect the details of two MS spectra, and reflect the resolution of the experimental native MS spectra. We first select top 20 pairs of peaks in the native spectra of rhEPO BRP and epoetin zeta, and then calculate the optimal bin width Woptimal at three different charge states ([M+8H]8+, [M+9H]9+, [M+10H]10+ for rhEPO), as illustrated in Supplementary Fig. 3a. The median of the 60 optimal bin width (for each peak pair, there are three optimal bin widths, in total there are 60 numbers) is used as the bin width for the correlation test.
To further verify the selection, we plot the correlation values over a series of bin widths (1 to 20 m/z with a step size 0.1, shown in blue) with a local polynomial regression fitting line shown in green. The selected bin width is close to the inflection point, as illustrated in Supplementary Fig. 3b.
The data that support the findings of this study are available on request from the corresponding author (A.J.R.H.).
The algorithm is written in R (version 3.3.1), and it is made publicly available and supplemented in Github. https://github.com/Yang0014/glycoNativeMS.
How to cite this article: Yang, Y. et al. Hybrid mass spectrometry approaches in glycoprotein analysis and their usage in scoring biosimilarity. Nat. Commun. 7, 13397 doi: 10.1038/ncomms13397 (2016).
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We acknowledge the support from the Netherlands Organization for Scientific Research (NWO) funding the large-scale proteomics facility Proteins@Work (project 184.032.201) embedded in the Netherlands Proteomics Centre. Y.Y. and A.J.R.H. are supported by the EU funded ITN project ManiFold, grant 317371. This project has received additional funding from the European Union’s Horizon 2020 research and innovation programme for MSMed, under grant agreement No. 686547. V.F. and A.J.R.H. acknowledge further support by the NWO TOP-Punt Grant 718.015.003.
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