N-glycan Profiling of Glycoproteins by Hydrophilic Interaction Liquid Chromatography with Fluorescence and Mass Spectrometric Detection

Summary

N-glycan profiling of glycoproteins is essential for discovering novel biomarkers and understanding glycan functions in cellular events. Additionally, N-glycan analysis of protein biopharmaceuticals is very important for human use. In this current article, a high-throughput strategy for identifying and quantifying N-glycan structures was presented using the HILIC-FLD-MS/MS technique.

Abstract

Glycosylation is a vital modification found in proteins. N-glycan profiling of glycoproteins is required to detect novel biomarker candidates and determine glycan alterations in diseases. Most commercially available biopharmaceutical proteins are glycoproteins. The efficacy of these drugs is affected by glycosylation patterns. Therefore, an in-depth characterization method for the N-glycans is necessary. Here, we present a comprehensive approach for qualitative and quantitative analysis of N-glycans using hydrophilic interaction liquid chromatography equipped with fluorescence detection and tandem mass spectrometry (HILIC-FLD-MS/MS). N-glycans were released from glycoproteins with a facile method and labeled by a procainamide fluorophore tag in the strategy. Subsequently, the procainamide labeled N-glycans were analyzed by a HILIC-FLD-MS/MS technique. In this approach, N-glycan structures were confirmed by the tandem mass spectrometric analysis, whereas fluorescence detection was used for the quantitative analysis. An application for data analysis of the detected N-glycan peaks is described in the study. This protocol can be applied to any glycoprotein extracted from various species.

Introduction

Glycosylation is a vital post-translational modification observed in proteins¹. Multiple enzymatical processes regulate glycosylation modification in cellular organisms. Glycans are attached to the proteins by these enzymatical processes, and the proteins subjected to this modification are called glycoproteins¹. Two glycosylation types are commonly observed in proteins. O-glycosylation is the attachment of O-glycans to the side chain of serine or threonine amino acid residues. N-glycosylation is the attachment of N-glycans to the side chain of asparagine amino acid residue in a protein.

The structure, stability, and folding of the proteins are affected by glycan attachments². The glycosylation process dramatically influences the functions of the proteins, and glycoproteins regulate many cellular functions in organisms^3,4. For example, heavily glycosylated proteins protect their glycoproteins from proteolytic degradation⁵. Another example is glycans of thyroid gland proteins that regulate Tg transport and hormone synthesis^6,7. To explain their roles in cellular events, an in-depth characterization of glycoproteins is required⁸.

N-glycan profiles of the glycoproteins change in disease situations^9,10,11,12. Profiling N-glycans derived from crucial glycoproteins or body fluids is required to discover novel biomarkers and understand the enzymatic activity changes in disease cases. On the other hand, most protein biopharmaceuticals are glycoproteins, and their glycan profiles influence drug efficacy¹³. Therefore, an acceptable method of N-glycan profiling must be performed in developing proper protein biopharmaceuticals for human use¹⁴.

Glycomics is an emerging discipline used to identify and quantify glycan structures of glycosylated molecules^15,16. Many methods have been utilized for profiling the glycans of glycosylated species, including NMR¹⁷ and MS¹⁸. Hydrophilic Interaction Liquid Chromatography-with Fluorescence Detection (HPLC-HILIC-FLD) is the gold standard method for profiling N-glycans derived from glycoproteins¹⁹. When this strategy is combined with mass spectrometric detection, identifying N-glycan structures could be easier and more reliable. Most fluorescence tags used in N-glycan analysis with mass spectrometry have low ionization efficiencies. In contrast, procainamide increases the ionization efficiencies of N-glycans, which is used to obtain efficient tandem mass spectra of N-glycan structures^20,21. Specific fragments can be obtained from this strategy by tandem mass spectrometry for the structural identification of N-glycans such as core fucosylated²² (proc-HexNAc1Fuc1) and bisecting types²³ (proc-Hex1HexNAc3, proc-Hex1HexNAc3Fuc1).

This study demonstrates a facile protocol for the N-glycan profiling of glycoproteins with HILIC-FLD-MS/MS. The presented method includes four steps: (1) releasing of N-glycans from glycoproteins (2) labeling of N-glycans by a procainamide tag (3) purification of the procainamide labeled N-glycans, and (4) data analysis.

Protocol

NOTE: The human plasma used is commercially available (Table of Materials). No further biological samples obtained from humans were used.

1. ​Glycan release

1. Denaturation of (glyco-)proteins
   1. Prepare the glycoprotein standards (e.g., IgG, a monoclonal antibody) at a concentration of a 10 µg·µL^-1 in deionized H₂O. For human plasma, the concentration used is 70 µg·µL^-1.
      NOTE: The samples should be vortexed until all solid proteins are dissolved. Human plasma (lyophilized) was used for the preparation of the plasma samples.
   2. Take 20 µL of glycoprotein samples (200 µg) and lyophilized human plasma (1.4 mg).
   3. Add 40 µL of 2% SDS (sodium dodecyl sulphate) (w/v).
   4. Incubate the samples at 60 °C for 10 min to denature the (glyco-)proteins.
      NOTE: The samples could be mixed at 500 rpm by a thermomixer during the incubation. A shaking water bath could be used alternatively.
2. Glycan release
   1. Add 20 µL of 4% Igepal-CA630 to the samples from step 1.1.4.
   2. Add 20 µL of 5x PBS (phosphate buffer saline).
   3. Prepare PNGase F enzyme at the concentration of 1 U·µL^-1 in deionized water.
   4. Add 1 U of enzyme for glycoprotein standards and 2 U of enzyme for human plasma samples.
   5. Incubate the samples at 37 °C for 16 h.
3. Procainamide labeling
   1. Prepare labeling solution using procainamide hydrochloric acid (110 mg·mL^-1 in DMSO/AA (dimethyl sulfoxide /glacial acetic acid) 7/3, v/v).
   2. Prepare reductive amination solution using sodium cyanoborohydride (65 mg·mL^-1 in DMSO/AA, 7/3, v/v).
      CAUTION: Sodium cyanoborohydride is very toxic and flammable. Wear eye shields. 2-picoline borane complex (107 mg·mL^-1 in DMSO) could be used alternatively.
   3. Mix these solutions in a ratio of 1:1, v/v to prepare the labeling mixture.
   4. Add 100 µL of this labeling mixture to the glycan released sample from step 1.2.5.
   5. Incubate the samples at 65 °C for 2 h.

2. Purification of Procainamide Labeled N- glycans by Solid-phase Extraction (SPE) Cartridge

1. Prepare a solution of microcrystalline cellulose (100 mg·mL^-1) in deionized water.
2. Take 300 µL of microcrystalline cellulose and insert it into the microcentrifuge tubes.
3. Wash the microcrystalline cellulose with 1 mL of deionized H₂O.
4. Wash the microcrystalline cellulose with 1 mL of ACN/MQ (acetonitrile/dH₂O), 85/15, v/v for conditioning.
   NOTE: The microcentrifuge should be used for 1 min to discard washing solutions carefully.
5. Take 120 µL of glycan release solution and mix with 680 µL of ACN to obtain proper loading conditions (85/15, v/v, ACN/sample).
6. Mix this mixture with microcrystalline cellulose in the microcentrifuge tubes.
7. Incubate it at room temperature in a thermomixer by shaking at 500 rpm for 15 min.
8. Transfer the slurry to an SPE cartridge (1 mL volume capacity).
   NOTE: Do not allow air to enter cartridge packing.
9. Discard the loading solutions by passing slowly (1 drop/second).
   NOTE: Ensure that the SPE system is connected to the vacuum pump. Solvents may flow with gravity. When necessary, apply vacuum via a vacuum pump. The applied vacuum pressure should be appropriately adjusted to transfer liquids down slowly.
10. Wash the sample by passing 1 mL of ACN/MQ/TFA (acetonitrile/dH₂O/trifluoroacetic acid) solution (85/14/1, v/v/v) twice.
11. Wash the sample by passing 1 mL of ACN/MQ mixture (85/15, v/v) twice.
12. Elute the procainamide labeled N-glycans with 0.75 mL of water.
13. Dry the elution solution with a concentrator overnight.
    NOTE: Use a concentrator temperature of 45 °C for drying.
14. Dissolve the dried samples in a mixture of 100 µL of ACN/MQ (75/25, v/v) and transfer this solution to the vials, including an insert.
    ​NOTE: The redissolved samples should be vortexed for 20 second.

3. HILIC-FLD-MS/MS Analysis

1. Insert Tee (T) adaptors to the HILIC column to separate the flow into the two equal volumes. Connect one of both to the FLD detector, the other to the MS detector.
   NOTE: The flow lines must be the same lengths.
2. Adjust a gradient program for HILIC separations of procainamide labeled N-glycans as indicated in Supplementary Figure 1. Use Mobile Phase A: 50 mM ammonium formate (pH: 4.4 and Mobile Phase B: 100 % ACN).
   NOTE: The gradient program could be further optimized depending on the glycan heterogeneity of samples.
3. Click the Sampler button and set the injection volume to 10 µL.
4. Click the Column Comp and adjust the column temperature to 60 °C.
5. Click FLD and adjust the FLD excitation and emission wavelengths to 310 nm and 370 nm, respectively.
6. Adjust the MS source, tune, and MS/MS parameters as displayed in Supplementary Figure 2.
   ​NOTE: The MS and MS/MS parameters could be changed depending on the mass spectrometry used in the analysis.

4. Data Analysis

1. Identification of procainamide labeled N-glycans
   1. Export MS/MS data by a proper format for database searches (e.g., .mgf, .xml).
   2. Insert them into a database search tool for the identification of N-glycans.
   3. Select the sample name listed in the software and click the Glycan Search button for the identification of procainamide labeled N-glycans by using the Carbbank database with given parameters (Supplementary Figure 3).
   4. Open the edit chromatograms button in the data analysis software for raw data and select extracted ion chromatogram type by filtering in all MSn.
   5. Add specific masses for core-fucosylated fragment proc-N1F1 (m/z 587.3⁺) and bisected fragments proc-H1N3 (m/z 1009.5⁺) and proc-H1N3F1 (m/z 1155.5⁺).
   6. Determine the precursors containing core-fucosylated and bisected N-glycan structure fragments.
   7. Export the identified N-glycan structures by the software (Supplementary Table 1-3).
   8. Check the precursors detected manually for determination of core-fucosylated and bisected N-glycan structures.
2. Quantification of procainamide labeled N-glycans by an open-source software²⁴
   1. Select FLD chromatogram in the chromatograms and click the method in the software. Open a method for exporting chromatograms as .xy file format.
   2. Convert the .xy file format of exported chromatograms to .txt files.
   3. Open the quantitative analysis software.
      NOTE: The software used in the study can be downloaded from a Github source (https://github.com/Tarskin/HappyTools).
   4. Follow the instructions and tutorials of the program presented by the developer.
      NOTE: It is recommended to use a batch process to export relative areas.
   5. Adjust the setting parameters (Supplementary Figure 4). Define four minimum peaks and 27 signal/noise ratios for calibrations.
   6. Open the results file with proper software such as Microsoft Excel for further evaluation.

Results

In this presented approach, the N-glycans were first released, labeled by the procainamide tag and purified by cellulose-containing SPE cartridges. Then, N-glycan analysis of IgG, trastuzumab, and human plasma were performed by an HPLC-HILIC-FLD-MS/MS system. The MS (base peak) and FLD chromatograms of the determined N-glycan structures obtained from IgG and trastuzumab are shown in Figure 1, respectively. The MS/MS data obtained from these analyses were imported t...

Discussion

N-glycan profiling of glycoproteins includes challenging steps. Although there are many different methodologies for this purpose, a suitable approach should be selected for both identification and quantification of N-glycan structures¹⁴. HILIC-FLD is the gold standard approach for the quantification of N-glycans. However, identification of all N-glycan types by FLD detection is not achieved. Therefore, tandem MS analysis is needed for confirming N-glyca...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Acetic acid	Carlo Erba Reagents	401413	Glacial RS For LC/MS
Acetonitrile	Merck	1000292500	LC-MS LiChrosolv
Agilent 1200 Series HPLC with 1260 Series FLD dedector	Agilent Technologies
Ammoniumm Formate	Carlo Erba Reagents	419741	For LC/MS
Bruker TIMS-TOF (Q-TOF) Mass Spectrometry	Bruker Daltonics
Cellulose	Sigma Aldrich	310697	microcrystalline, powder, 20 μm
Deionized Water	Carlo Erba Reagents	412111	For LC/MS
Dimethyl sulfoxide	Sigma Aldrich	41639	BioUltra, for molecular biology, ≥99.5% (GC)
Empty polypropylene SPE Tube with PE frits	Sigma Aldrich	54220	20 μm porosity,volume 1 mL
Extraction Manifold, 20-position	Waters	WAT200607	Complete with rack for 13 x 100 mm tubes
Human Plasma	Sigma Aldrich	P9523	lyophilized
IGEPAL CA-630	Sigma Aldrich	I8896	for molecular biology
IgG	Sigma Aldrich	I4506	lyophilized powder
Phosphate buffered saline	Sigma Aldrich	P4417	Tablet
PNGase F enzyme	Promega	V483A
Procainamide hydrochloride	abcam	ab120955
Sodium cyanoborohydride	Sigma Aldrich	156159	reagent grade, 95%
Sodium dodecyl sulfate	Sigma Aldrich	71725
trastuzumab	Roche Diagnostics
Trifluoroacetic acid	Sigma Aldrich	302031	for HPLC, ≥99.9%