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©2015 Waters Corporation 1
The Road to Glycan Analysis
Without Compromise
WCBP 2015
Waters Technical Seminar
Jan 27, 2015 Washington, DC
©2015 Waters Corporation 2
Today’s Agenda
 Overview and Introduction
 RapiFluor-MS N-Glycan Labeling: A breakthrough
technology for released glycan LC and MS analysis
Matthew A. Lauber (Consumables Business Unit, Waters)
 RapiFluor-MS Technology & Glycan Characterization
Ying Qing Yu (Biopharmaceutical Sciences, Waters)
 Impact of RapiFluor-MS Technology
on Released Glycan Profile Monitoring
Sean M. McCarthy (Biopharmaceutical Sciences, Waters)
 Scientific Panel – Questions & Discussion
©2015 Waters Corporation 3
Rapid Preparation
Deglycosylation
Labeling
SPE
30 min
High Sensitivity
HILIC-Fluorescence-MS
Fluorophore
+MS Charge Tag
Fluorescence MS
Glycosylation of Biotherapeutics
N-glycolylneuraminic acid
Fucose
GlcNAc
Mannose
Galactose
N-acetylneuraminic acid
Immunogenic
(αGal / N-glycolylneuraminic acid)
Low Half Life
(high mannose)
Anti-Inflammatory
(sialylation)
Effector Functions (ADCC/CDC)
(fucosylation/galactosylation)
Overall profile sensitive to
manufacturing conditions
 N-glycosylation is a quality attribute
of biotherapeutics
 Glycosylation profiles are characterized
and routinely monitored
Anal Chem 2013, 85 (2), 715-36.
©2015 Waters Corporation 4
Glycoprotein Characterization
Multiple Strategies – Complementary Information
©2015 Waters Corporation 5
Customer voice brought us focus
Compatible with both
MS and optical
detection
Just compatible with
MS detection
Just compatible with
Fluorescence
Providesrapid labeling
versusmany existing
offerings
Just compatible with
UV detection
Reagents are less toxic
versusmany existing
offerings Lower cost per sample
Labelingreagent and
protocol is automation
friendly.
1.7
1.8
1.9
2
2.1
2.2
2.3
0 20 40 60 80 100 120 140
Mean
Mentions
MoreImportantLessImportant
Lower Interest Higher Interest
©2015 Waters Corporation 6
Rapid
or
Traditional
LC or LCMS
Quan or Qual
Cost/ROI
Training
Requirements
The Road to Glycan Analysis Without Compromise
RELEASED GLYCAN ANALYSIS
©2015 Waters Corporation 7
RapiFluor-MS N-Glycan Labeling:
A breakthrough technology for
released glycan LC and MS analysis
©2015 Waters Corporation 8
Rapid Preparation
Deglycosylation
Labeling
SPE
30 min
High Sensitivity
HILIC-Fluorescence-MS
Fluorophore
+MS Charge Tag
Fluorescence MS
Released Glycan Analysis
HILIC Profiling
5 Hours
to
2 Days
0.0E+0
FLR
Conventional
2-AB
5.3e2
m/z
500 1000 1500 2000
%
0
100
m/z
500 1000 1500 2000
%
0
100
m/z
500 1000 1500 2000
%
0
100
m/z
500 1000 1500 2000
%
0
100
RapiFluorMS_hIgG_14pmol_18Nov14_04 283 (5.065)
3.47e6
2AB_hIgG_halfload_20Nov14_10 235 (4.234)
2.89e4
2AB_hIgG_halfload_20Nov14_10 495 (8.689)
529
RapiFluorMS_hIgG_14pmol_18Nov14_04 507 (8.892)
1.15e5
500 2000 m/z
2+
MS
©2015 Waters Corporation 9
N-Glycan
(Glycosylamine)
N-Glycan
( Acyclic Free Reducing End)
Mild Acid
Hydrolysis
PNGase F
+
ProteinN-Glycan
Released N-Glycan
(Glycosylamine)
Protein
+
HOAc
DMSO
N-Glycan
(Free Reducing End) 2-AB
N-Glycan
(2-AB Labeled)
Reduction
NaBH3CN
SPE
Reductive Amination
(conventional)
• Anhydrous sample
• Numerous chemical
conversions
• Laborious
• Heterogenous reaction
products
Rapid Tagging
Glycosylamine
labeling circumvents
these issues
Out with Conventions
Reductive Amination is Laborious
©2015 Waters Corporation 10
RapiFluor-MSTM Reagent
Built Upon Our Expertise
From Waters’ expertise in rapid,
fluorescence labeling of amino acids
Enhanced chemical properties for glycan analysis:
• Rapid Tagging
• Efficient Fluorescence
• Enhanced Ionization Efficiency
AccQ·Fluor™
Rapid
Fluorescence
Patent Pending
RapiFluor-MS
©2015 Waters Corporation 11
+
+
H2O
+ + CO2
rapiFluor-MS
Monoisotopic mass shift
(from glycosylamine)
312.1586 Da
Glycosylamine
+C17H20N4O2
RapiFluor-MS Reagent
Rapid Reaction Kinetics
NHS Carbamate
Rapid Tagging Group
Tertiary Amine
MS-Active Charge Tag
Reaction Time = Seconds
Procedure Time:
Quinoline Fluorophore
Glycan
Glycan
Highly stable urea linkage
ΔMass
312 Da
©2015 Waters Corporation 12
RapiFluor-MS Reagent
Sensitivity Comparison – Instant AB
0.0E+0
2.6E+6
4.5 5.0 5.5 6.0 6.5 7.0 7.5
0.0E+0
2.6E+6
4.5 5 5.5 6 6.5 7 7.5
0.0E+0
1.7E+6
4.5 5 5.5 6 6.5 7 7.5
0.0E+0
3.0E+3
4.5 5 5.5 6 6.5 7 7.5
0.0E+0
1.7E+6
4.5 5 5.5 6 6.5 7 7.5
FLR
MS
(BPI)
FLR
MS
(BPI)
FA2
FA2
FA2
FA2
RapiFluor-MS™ Labeled N-Glycans
Instant AB™ Labeled N-Glycans
min
min
RapiFluor-MSTM Labeled N-Glycans
Instant ABTM Labeled N-Glycans
Instant AB is a trademark of Prozyme Inc.
300X
Zoom
©2015 Waters Corporation 13
RapiFluor-MS Reagent
Sensitivity Comparison – Instant AB
0.0E+0
2.6E+6
4.5 5.0 5.5 6.0 6.5 7.0 7.5
0.0E+0
2.6E+6
4.5 5 5.5 6 6.5 7 7.5
0.0E+0
1.7E+6
4.5 5 5.5 6 6.5 7 7.5
0.0E+0
3.0E+3
4.5 5 5.5 6 6.5 7 7.5
0.0E+0
1.7E+6
4.5 5 5.5 6 6.5 7 7.5
FLR
MS
(BPI)
FLR
MS
(BPI)
342.8
179.9
233.7
0.3
0
100
200
300
400
Compound 4 Compound 1
ReponseFactors
(FA2PeakAreaperSampleofN-Glycans
from1µgofAnti-CitrininIgG/1000)
FA2
FA2
FA2
FA2
RapiFluor-MS
Labeled
Instant AB
Labeled
FLR
MS
(BPI)
ResponseFactors
RapiFluor-MS Labeled N-Glycans
Instant AB Labeled N-Glycans
min
min
~2x
nearly
1000x
300x
Zoom
©2015 Waters Corporation 14
0
10
20
30
40
50
60
70
80
90
100
0
10
20
30
40
50
60
70
80
90
100
0
10
20
30
40
50
60
70
80
90
100
Fluorescence MS (BPI)
Instant AB Labeled
RapiFluor-MS Labeled
2-AB Labeled
RelativePerformance(%)
52.5
7.0
0.1 0.6
Procainamide Labeled
0
10
20
30
40
50
60
70
80
90
100
30.0*
7.0*
(*) Comparative result extrapolated from a published comparison of N-glycans,
wherein it was found that procainamide provided comparable fluorescence and up to
50 fold greater ESI-MS sensitivity when compared to 2-AB(Klapoetke et al. 2010).
RapiFluor-MS Reagent
Sensitivity Comparison
©2015 Waters Corporation 15
10 min 5 min 10 min
30 min
Patent Pending
Simplified Workflow
Total
Sample Prep Time
Conventional
5 Hours
to
2 Days
GlycoWorks™
RapiFluor-MS™ N-Glycan Kit
Direct Analysis
(Organic Solvent Dilution)
©2015 Waters Corporation 16
Rapid Deglycosylation
RapiGest™ SF Assisted
1% RapiGest SF
Surfactant
2 min
≥80˚C
GlycoWorks
Rapid Buffer
5 min
50˚C
GlycoWorks
Rapid PNGase F
Enzymatic
Deglycosylation
©2015 Waters Corporation 17
140000 145000 150000 1550
%
0
100
VicamIgG_PNGaseFnoDTT_7p5ug_100414 638 (10.803) M1 [Ev-612128,
145345
mass
140000 145000 150000 155000 160000
%
0
100
VicamIgG_PNGaseFnoDTT_7p5ug_100414 654 (11.074) M1 [Ev-629947,It13] (Gs,1.500,1955:4983,1.00,L30,R30); Cm
3.49e3146786
146952
mass
140000 145000 150000 155000 160000
%
0
100
VicamIgG_PNGaseFnoDTT_7p5ug_100414 671 (11.361) M1 [Ev-562807,It10] (Gs,1.500,1993:5000,1.00,L30,R30); Cm (666:679)
352148401
148240
148560148.4 kDa
145.3 kDa
146.8 kDa
2 Step
2 min
Heat Denaturation
5 min
50˚C
5 min
50˚C
No PNGase F
(control)
Rapid Deglycosylation
RapiGest™ SF Assisted
©2015 Waters Corporation 18
Labeled Glycan
Labeled Deglycosylated Protein
Byproducts
Collect
Labeled Glycan
Reaction Byproducts
Robust HILIC SPE
©2015 Waters Corporation 19
0.0E+0
1.2E+6
10 15 20 25 30 35
Positive Control
0.0E+0
1.2E+6
10 15 20 25 30 35
2x SPE
FA2
FA2G2S1
A3S1G3S3
1x SPE
0
5
10
15
20
25
30
RelativeAbundance(%)
Positive
Control
SPE
Processed
A3G3S3
1x SPE
2x SPE
min
5.7%
6.1%
 GlycoWorks HILIC SPE of RapiFluor-MS N-glycans is quantitative
 No significant deviation in the glycan profile upon SPE processing
FLR
hIgG and fetuin N-glycans
Robustness
Quantitative Extraction
FLR
©2015 Waters Corporation 22
FA2
Rep #1
1.6 pmol
Rep #2
1.7 pmol
100% Theoretical Yield = 2.3 pmol
1.5x107 pg IgG 1 pmol
150,000 pg
2 pmol glycan
1 pmol IgG
0.45 pmol FA2
1 pmol total
glycan pool
10 μL injection
400 μL
sample
prepared
X X X X = 2.3 pmol
Step Yield Testing to confirm minimal bias
Deglycosylation Complete
 Intact mass analysis
 Gel shift assays
 Subunit LC-MS
Labeling >95%  Released glycan profile vs subunit derived glycan information
SPE ~74%
 Recovery measurements
 Glycan profile before vs after SPE
Entire Workflow
(experimentally
determined)
~73% Yield
Robustness
High Yield and Minimal Bias
0E+0
2E+6
3 4 5 6 7 8 9 10 11 12 13
©2015 Waters Corporation 23
Summary
GlycoWorks™ RapiFluor-MS™ N-Glycan Kit
 Simple, streamlined protocol
 Fast and complete deglycosylation
 Rapid and efficient labeling
 Unbiased and robust SPE for neutral to
tetrasialylated N-glycans
 Unprecedented FLR and MS sensitivity
GlycoWorks
RapiFluor-MS N-Glycan Kit
RapiFluor-MS
Glycoprotein
Analysis-Ready N-glycans
30 min
©2015 Waters Corporation 24
GlycoWorks™ RapiFluor-MS™ Kit
Smart Workflow with No Compromise
Available
February 2015
©2015 Waters Corporation 25
Poster
WCBP 2015 Poster P-216-W
Rapid Preparation
of N-Glycans Using a Novel
Fluorescence and MS Active
Labeling Reagent
Download pdf
©2015 Waters Corporation 26
RapiFluor-MS:
Enhanced Workflows
for Glycan Characterization
©2015 Waters Corporation 27
Glycan Characterization
 ACQUITY UPLC® H-Class Bio System
 ACQUITY UPLC Column Manager
 ACQUITY UPLC FLR Detector
 Xevo® G2-XS QTof MS
 UNIFI® Glycan Application Solution
or MassLynx® Informatics
 GlycoWorks™ RapiFluor-MS™ N-Glycan Kit
 ACQUITY UPLC Glycan BEH Amide Column
©2015 Waters Corporation 28
UNIFI® Glycan Workflows
Workflows support conventional glycan labels
and new RapiFluor-MS™ label technology
HILIC FLR
GU +Accurate Mass
HILIC FLR
GU + DDA MS/MS
Automated
Data
Acquisition
Processing
Review and
Reporting
©2015 Waters Corporation 29
RapiFluor-MS™ Labeling for Characterization
Greater than 100x MS response over 2AB labeling
BPI MS
Sample: NIST RM 8670 mAb lot #3F1b
©2015 Waters Corporation 30
HILIC FLR GU + Accurate Mass
RapiFluor-Dextran Ladder
Retention Time Calibration Curve
Assign GU values to N-glycans
BPI MS for accurate mass confirmation
GU
Method Robustness and Transferability, Confident Assignments
RapiFluor-MS Labeled Dextran and System Performance Standard
(hIgG) are now available to support this GU workflow
©2015 Waters Corporation 31
UNIFI ® Scientific Library for Automated
GU or GU+Mass Glycan Confirmation
Experimental
GU value
FLR label
mass
Waters Glycan GU Library:
• Experimentally derived GU Retention (>10 injections/protein)
• Data from proteins representing spectrum of glycan diversity
• All entries confirmed with exoglycosidase digestion
©2015 Waters Corporation 32
UNIFI® Scientific Library for
Confident Glycan Assignments
©2015 Waters Corporation 33
Powerful UNIFI® Reporting Architecture
Simplifies Communication of Results
Example
©2015 Waters Corporation 34
UNIFI® Glycan DDA Workflow
©2015 Waters Corporation 35
Optional UNIFI® Export to SimGlycan
for MS/MS Database Search
A2G2S1
©2015 Waters Corporation 36
Enhanced MS/MS with RapiFluor-MS™ Labeling
FLR
BPI MS
MSMS
MS performance extends to fragmentation data
©2015 Waters Corporation 37
Enhanced MSMS with RapiFluor-MS Labeling
MS performance extends to MS/MS fragmentation data
©2015 Waters Corporation 38
Poster
WCBP 2015 Poster P-115-T
Developing a Scientific
Library for UPLC/FLR/MS
Analysis of Released
N-glycans Labeled with a
Novel Labeling Reagent
Download pdf
©2015 Waters Corporation 39
RapiFluor-MS:
Enhanced Workflows
for Glycan Monitoring
©2015 Waters Corporation 40
30.0010.00 12.00 14.00 16.00 18.00 20.00 22.00 24.00 26.00 28.00
24.00 28.00 32.00 36.00 40.00 44.00 48.00 52.00 56.00 60.00 64.00
Alliance HPLC
XBridge Glycan BEH Amide, 130Å, 2.5µm
3.0 X 225 mm total length (150 mm + 75 mm)
Flow Rate: 0.56 mL/minute
H-Class BIO UPLC
ACQUITY UPLC Glycan BEH Amide, 130Å, 1.7µm
2.1 X 150 mm
Flow Rate: 0.40 mL/minute
Total Run Time = 55 minutes
Total Run Time = 121.3 minutes
Fluorescence(relative)
Time (minutes)
 Comparable sensitivity and resolution – 3x sample load / 2x increase in time
 Transfer between labs with different LC equipment capabilities
Transferability between UPLC® and HPLC
RapiFluor-MS™ Labeled Glycans
©2015 Waters Corporation 41
Glycan Monitoring
 ACQUITY UPLC® H-Class Bio System
 ACQUITY UPLC Column Manager
 ACQUITY UPLC FLR Detector
 ACQUITY® QDa® Mass Detector
 Empower® or MassLynx® Informatics
 GlycoWorks™ RapiFluor-MS™ N-Glycan Kit
 ACQUITY UPLC Glycan BEH Amide Column
©2015 Waters Corporation 42
ACQUITY® QDa® Mass Detector
A breakthrough product with mass appeal
 Revolutionary innovative design
focused on ease of use for analysts
 Empowering analytical chemists
everywhere with orthogonal mass
detection – added information with
every sample
 Compact, robust and affordable:
Built for constant use with a wide
variety of chromatographic conditions
 Seamlessly integrates with
Empower based HPLC & UPLC®
©2015 Waters Corporation 43
Automated Start Up Provides
Robust, Reproducible Performance
 Automated resolution and calibration occurs with each start-up
ensuring mass information is accurate and precise
 ESI interface optimized for UPLC® performance to ensure
chromatographic resolution, sensitivity and throughput is preserved
 Disposable sample aperature and capillary for easy maintenance
Graphic QDa®
monitor display
enables easy
viewing and
adjustment of
system parameters
©2015 Waters Corporation 44
Routine N-Glycan Detection with
Comparable FLR and MS response
Minutes
5 10 15 20 25 30 35 40
Minutes
5 10 15 20 25 30 35 40
Detection across a broad
range of glycoforms:
IgG
Simple bi-antennery
structures
RNase B
High mannose
structures
Fetuin
Large, complex
structures
©2015 Waters Corporation 45
IgG Glycan Profile and Structure
Confirmation Using ACQUITY® QDa®
Key take away: Large dynamic range – can clearly see
most abundant and least abundant glycoforms.
0.00
240.00
480.00
Intensity
0.0
1.6x106
3.2x10 6
Minutes
10.00 15.00 20.00 25.00 30.00
896.0
Intensity
0.0
12000.0
24000.0
m/z
600 1200
A2G1b
0.5% RPA
888.2
Intensity
0
300000
600000
m/z
600 1200
FA2
20.5% RPA
EU
©2015 Waters Corporation 46
Intuitive GMP compliant Reporting
Empower® integration enables annotation of peaks with names and m/z
A2-815.1
FA2-888.2
FA2B-989.6
A2G1a-896.2
A2G1b-896.0
FA2G1a-969.3
FA2G1b-969.2
FA2BG1a-1070.7
FA2BG1b-1070.6
A2G2-977.1
FA2G2-1050.3
FA2BG2-1151.8
FA2G1S1-1114.6
FA2G2S1-1196.0
FA2BG2S1-865.3
FA2G2S2-894.7
FA2BG2S2-962.2
0.00
240.00
480.00
Minutes
10.00 15.00 20.00 25.00 30.00
EU
©2015 Waters Corporation 47
Developing a Rapid Method
for Glycan Analysis
EU
0
10
20
30
40
Minutes
2 3 4 5
10 minute
Method
EU
0
10
20
Minutes
5 10 15 20
55 minute
Method
©2015 Waters Corporation 48
Rapid Screening Process
for Development Samples
EU
0
20
40 FLR
Intensity
0
1x106
2x106
Minutes
1 2 3 4 5 6
SIR Overlay
Trastuzumab N-Glycan Analysis
RapiFluor-MS™ labeled glycans: 10 minute method
Intensity
0
50000
Intensity
0
200000
Intensity
0
1x10
6
2x10
6
Intensity
0
50000
100000
Intensity
0
1x10
6
Intensity
0
200000
400000
Intensity
0
20000
Minutes
1 2 3 4 5 6
A2G(4)1
895.9 m/z
F(6)A2
887.9 m/z
F(6)A2G(4)1
968.9 m/z
F(6)A2G(4)2
1049.9 m/z
A2
814.8 m/z
F(6)A2G(4)2S1
1195.5 m/z
M5
774.1 m/z
©2015 Waters Corporation 49
Monitoring Glycan Ratios
Keeping Tabs on Mannose 5
Mannose 5 spiked in
Low Medium High
Inj 1 0.61 0.96 1.20
Inj 2 0.57 0.90 1.11
Inj 3 0.55 0.86 1.18
Mean 0.58 0.91 1.16
StDev 0.03 0.05 0.04
% RSD 5.44 5.47 3.85
Intensity
0
60000
120000
180000
240000
Minutes
2.00 2.50 3.00 3.50 4.00
Intensity
0.0
35000.0
70000.0
105000.0
140000.0
Minutes
2.00 2.50 3.00 3.50 4.00
F(6)A2G(4)1
SIR: 968.9 m/z
M5
SIR: 774.1 m/z
Man5: F(6)A2G(4)1 Ratio
©2015 Waters Corporation 50
Released N-Glycan UPLC Analysis Workflows
SAMPLE PREP SEPARATION
DETECTION &
INFORMATICS
GlycoWorks™ Kits
RapiFluor-MS™
N-Glycan Kit
ACQUITY® FLR/QDa
and Empower® 3
Software
FLR/Xevo® G2-XS QTof MS
and UNIFI® Scientific
Information System
ACQUITY UPLC®
Glycan BEH
Amide Column
Deglycosylation, Labeling
and Clean-up in 30 min
Unmatched sensitivity
for FLR and MS detection
FLR Quantification
GU Retention
MS Confirmation
FLR Quantification
GU Retention
Accurate Mass
Confirmation
MS/MS Fragmentation
FLR
TIC
MS/MS
©2015 Waters Corporation 51
Poster
WCBP 2015 Poster P-206-W
Routine Monitoring of
N-Glycans Using a Novel
Labeling Reagent with
Fluorescence and Mass
Detection
Download pdf
©2015 Waters Corporation 52
RapiFluor-MS N-Glycan Labeling:
A breakthrough technology for
released glycan LC and MS analysis

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From WCBP 2015: GlycoWorks RapiFluor-MS for Glycan Profiling

  • 1. ©2015 Waters Corporation 1 The Road to Glycan Analysis Without Compromise WCBP 2015 Waters Technical Seminar Jan 27, 2015 Washington, DC
  • 2. ©2015 Waters Corporation 2 Today’s Agenda  Overview and Introduction  RapiFluor-MS N-Glycan Labeling: A breakthrough technology for released glycan LC and MS analysis Matthew A. Lauber (Consumables Business Unit, Waters)  RapiFluor-MS Technology & Glycan Characterization Ying Qing Yu (Biopharmaceutical Sciences, Waters)  Impact of RapiFluor-MS Technology on Released Glycan Profile Monitoring Sean M. McCarthy (Biopharmaceutical Sciences, Waters)  Scientific Panel – Questions & Discussion
  • 3. ©2015 Waters Corporation 3 Rapid Preparation Deglycosylation Labeling SPE 30 min High Sensitivity HILIC-Fluorescence-MS Fluorophore +MS Charge Tag Fluorescence MS Glycosylation of Biotherapeutics N-glycolylneuraminic acid Fucose GlcNAc Mannose Galactose N-acetylneuraminic acid Immunogenic (αGal / N-glycolylneuraminic acid) Low Half Life (high mannose) Anti-Inflammatory (sialylation) Effector Functions (ADCC/CDC) (fucosylation/galactosylation) Overall profile sensitive to manufacturing conditions  N-glycosylation is a quality attribute of biotherapeutics  Glycosylation profiles are characterized and routinely monitored Anal Chem 2013, 85 (2), 715-36.
  • 4. ©2015 Waters Corporation 4 Glycoprotein Characterization Multiple Strategies – Complementary Information
  • 5. ©2015 Waters Corporation 5 Customer voice brought us focus Compatible with both MS and optical detection Just compatible with MS detection Just compatible with Fluorescence Providesrapid labeling versusmany existing offerings Just compatible with UV detection Reagents are less toxic versusmany existing offerings Lower cost per sample Labelingreagent and protocol is automation friendly. 1.7 1.8 1.9 2 2.1 2.2 2.3 0 20 40 60 80 100 120 140 Mean Mentions MoreImportantLessImportant Lower Interest Higher Interest
  • 6. ©2015 Waters Corporation 6 Rapid or Traditional LC or LCMS Quan or Qual Cost/ROI Training Requirements The Road to Glycan Analysis Without Compromise RELEASED GLYCAN ANALYSIS
  • 7. ©2015 Waters Corporation 7 RapiFluor-MS N-Glycan Labeling: A breakthrough technology for released glycan LC and MS analysis
  • 8. ©2015 Waters Corporation 8 Rapid Preparation Deglycosylation Labeling SPE 30 min High Sensitivity HILIC-Fluorescence-MS Fluorophore +MS Charge Tag Fluorescence MS Released Glycan Analysis HILIC Profiling 5 Hours to 2 Days 0.0E+0 FLR Conventional 2-AB 5.3e2 m/z 500 1000 1500 2000 % 0 100 m/z 500 1000 1500 2000 % 0 100 m/z 500 1000 1500 2000 % 0 100 m/z 500 1000 1500 2000 % 0 100 RapiFluorMS_hIgG_14pmol_18Nov14_04 283 (5.065) 3.47e6 2AB_hIgG_halfload_20Nov14_10 235 (4.234) 2.89e4 2AB_hIgG_halfload_20Nov14_10 495 (8.689) 529 RapiFluorMS_hIgG_14pmol_18Nov14_04 507 (8.892) 1.15e5 500 2000 m/z 2+ MS
  • 9. ©2015 Waters Corporation 9 N-Glycan (Glycosylamine) N-Glycan ( Acyclic Free Reducing End) Mild Acid Hydrolysis PNGase F + ProteinN-Glycan Released N-Glycan (Glycosylamine) Protein + HOAc DMSO N-Glycan (Free Reducing End) 2-AB N-Glycan (2-AB Labeled) Reduction NaBH3CN SPE Reductive Amination (conventional) • Anhydrous sample • Numerous chemical conversions • Laborious • Heterogenous reaction products Rapid Tagging Glycosylamine labeling circumvents these issues Out with Conventions Reductive Amination is Laborious
  • 10. ©2015 Waters Corporation 10 RapiFluor-MSTM Reagent Built Upon Our Expertise From Waters’ expertise in rapid, fluorescence labeling of amino acids Enhanced chemical properties for glycan analysis: • Rapid Tagging • Efficient Fluorescence • Enhanced Ionization Efficiency AccQ·Fluor™ Rapid Fluorescence Patent Pending RapiFluor-MS
  • 11. ©2015 Waters Corporation 11 + + H2O + + CO2 rapiFluor-MS Monoisotopic mass shift (from glycosylamine) 312.1586 Da Glycosylamine +C17H20N4O2 RapiFluor-MS Reagent Rapid Reaction Kinetics NHS Carbamate Rapid Tagging Group Tertiary Amine MS-Active Charge Tag Reaction Time = Seconds Procedure Time: Quinoline Fluorophore Glycan Glycan Highly stable urea linkage ΔMass 312 Da
  • 12. ©2015 Waters Corporation 12 RapiFluor-MS Reagent Sensitivity Comparison – Instant AB 0.0E+0 2.6E+6 4.5 5.0 5.5 6.0 6.5 7.0 7.5 0.0E+0 2.6E+6 4.5 5 5.5 6 6.5 7 7.5 0.0E+0 1.7E+6 4.5 5 5.5 6 6.5 7 7.5 0.0E+0 3.0E+3 4.5 5 5.5 6 6.5 7 7.5 0.0E+0 1.7E+6 4.5 5 5.5 6 6.5 7 7.5 FLR MS (BPI) FLR MS (BPI) FA2 FA2 FA2 FA2 RapiFluor-MS™ Labeled N-Glycans Instant AB™ Labeled N-Glycans min min RapiFluor-MSTM Labeled N-Glycans Instant ABTM Labeled N-Glycans Instant AB is a trademark of Prozyme Inc. 300X Zoom
  • 13. ©2015 Waters Corporation 13 RapiFluor-MS Reagent Sensitivity Comparison – Instant AB 0.0E+0 2.6E+6 4.5 5.0 5.5 6.0 6.5 7.0 7.5 0.0E+0 2.6E+6 4.5 5 5.5 6 6.5 7 7.5 0.0E+0 1.7E+6 4.5 5 5.5 6 6.5 7 7.5 0.0E+0 3.0E+3 4.5 5 5.5 6 6.5 7 7.5 0.0E+0 1.7E+6 4.5 5 5.5 6 6.5 7 7.5 FLR MS (BPI) FLR MS (BPI) 342.8 179.9 233.7 0.3 0 100 200 300 400 Compound 4 Compound 1 ReponseFactors (FA2PeakAreaperSampleofN-Glycans from1µgofAnti-CitrininIgG/1000) FA2 FA2 FA2 FA2 RapiFluor-MS Labeled Instant AB Labeled FLR MS (BPI) ResponseFactors RapiFluor-MS Labeled N-Glycans Instant AB Labeled N-Glycans min min ~2x nearly 1000x 300x Zoom
  • 14. ©2015 Waters Corporation 14 0 10 20 30 40 50 60 70 80 90 100 0 10 20 30 40 50 60 70 80 90 100 0 10 20 30 40 50 60 70 80 90 100 Fluorescence MS (BPI) Instant AB Labeled RapiFluor-MS Labeled 2-AB Labeled RelativePerformance(%) 52.5 7.0 0.1 0.6 Procainamide Labeled 0 10 20 30 40 50 60 70 80 90 100 30.0* 7.0* (*) Comparative result extrapolated from a published comparison of N-glycans, wherein it was found that procainamide provided comparable fluorescence and up to 50 fold greater ESI-MS sensitivity when compared to 2-AB(Klapoetke et al. 2010). RapiFluor-MS Reagent Sensitivity Comparison
  • 15. ©2015 Waters Corporation 15 10 min 5 min 10 min 30 min Patent Pending Simplified Workflow Total Sample Prep Time Conventional 5 Hours to 2 Days GlycoWorks™ RapiFluor-MS™ N-Glycan Kit Direct Analysis (Organic Solvent Dilution)
  • 16. ©2015 Waters Corporation 16 Rapid Deglycosylation RapiGest™ SF Assisted 1% RapiGest SF Surfactant 2 min ≥80˚C GlycoWorks Rapid Buffer 5 min 50˚C GlycoWorks Rapid PNGase F Enzymatic Deglycosylation
  • 17. ©2015 Waters Corporation 17 140000 145000 150000 1550 % 0 100 VicamIgG_PNGaseFnoDTT_7p5ug_100414 638 (10.803) M1 [Ev-612128, 145345 mass 140000 145000 150000 155000 160000 % 0 100 VicamIgG_PNGaseFnoDTT_7p5ug_100414 654 (11.074) M1 [Ev-629947,It13] (Gs,1.500,1955:4983,1.00,L30,R30); Cm 3.49e3146786 146952 mass 140000 145000 150000 155000 160000 % 0 100 VicamIgG_PNGaseFnoDTT_7p5ug_100414 671 (11.361) M1 [Ev-562807,It10] (Gs,1.500,1993:5000,1.00,L30,R30); Cm (666:679) 352148401 148240 148560148.4 kDa 145.3 kDa 146.8 kDa 2 Step 2 min Heat Denaturation 5 min 50˚C 5 min 50˚C No PNGase F (control) Rapid Deglycosylation RapiGest™ SF Assisted
  • 18. ©2015 Waters Corporation 18 Labeled Glycan Labeled Deglycosylated Protein Byproducts Collect Labeled Glycan Reaction Byproducts Robust HILIC SPE
  • 19. ©2015 Waters Corporation 19 0.0E+0 1.2E+6 10 15 20 25 30 35 Positive Control 0.0E+0 1.2E+6 10 15 20 25 30 35 2x SPE FA2 FA2G2S1 A3S1G3S3 1x SPE 0 5 10 15 20 25 30 RelativeAbundance(%) Positive Control SPE Processed A3G3S3 1x SPE 2x SPE min 5.7% 6.1%  GlycoWorks HILIC SPE of RapiFluor-MS N-glycans is quantitative  No significant deviation in the glycan profile upon SPE processing FLR hIgG and fetuin N-glycans Robustness Quantitative Extraction FLR
  • 20. ©2015 Waters Corporation 22 FA2 Rep #1 1.6 pmol Rep #2 1.7 pmol 100% Theoretical Yield = 2.3 pmol 1.5x107 pg IgG 1 pmol 150,000 pg 2 pmol glycan 1 pmol IgG 0.45 pmol FA2 1 pmol total glycan pool 10 μL injection 400 μL sample prepared X X X X = 2.3 pmol Step Yield Testing to confirm minimal bias Deglycosylation Complete  Intact mass analysis  Gel shift assays  Subunit LC-MS Labeling >95%  Released glycan profile vs subunit derived glycan information SPE ~74%  Recovery measurements  Glycan profile before vs after SPE Entire Workflow (experimentally determined) ~73% Yield Robustness High Yield and Minimal Bias 0E+0 2E+6 3 4 5 6 7 8 9 10 11 12 13
  • 21. ©2015 Waters Corporation 23 Summary GlycoWorks™ RapiFluor-MS™ N-Glycan Kit  Simple, streamlined protocol  Fast and complete deglycosylation  Rapid and efficient labeling  Unbiased and robust SPE for neutral to tetrasialylated N-glycans  Unprecedented FLR and MS sensitivity GlycoWorks RapiFluor-MS N-Glycan Kit RapiFluor-MS Glycoprotein Analysis-Ready N-glycans 30 min
  • 22. ©2015 Waters Corporation 24 GlycoWorks™ RapiFluor-MS™ Kit Smart Workflow with No Compromise Available February 2015
  • 23. ©2015 Waters Corporation 25 Poster WCBP 2015 Poster P-216-W Rapid Preparation of N-Glycans Using a Novel Fluorescence and MS Active Labeling Reagent Download pdf
  • 24. ©2015 Waters Corporation 26 RapiFluor-MS: Enhanced Workflows for Glycan Characterization
  • 25. ©2015 Waters Corporation 27 Glycan Characterization  ACQUITY UPLC® H-Class Bio System  ACQUITY UPLC Column Manager  ACQUITY UPLC FLR Detector  Xevo® G2-XS QTof MS  UNIFI® Glycan Application Solution or MassLynx® Informatics  GlycoWorks™ RapiFluor-MS™ N-Glycan Kit  ACQUITY UPLC Glycan BEH Amide Column
  • 26. ©2015 Waters Corporation 28 UNIFI® Glycan Workflows Workflows support conventional glycan labels and new RapiFluor-MS™ label technology HILIC FLR GU +Accurate Mass HILIC FLR GU + DDA MS/MS Automated Data Acquisition Processing Review and Reporting
  • 27. ©2015 Waters Corporation 29 RapiFluor-MS™ Labeling for Characterization Greater than 100x MS response over 2AB labeling BPI MS Sample: NIST RM 8670 mAb lot #3F1b
  • 28. ©2015 Waters Corporation 30 HILIC FLR GU + Accurate Mass RapiFluor-Dextran Ladder Retention Time Calibration Curve Assign GU values to N-glycans BPI MS for accurate mass confirmation GU Method Robustness and Transferability, Confident Assignments RapiFluor-MS Labeled Dextran and System Performance Standard (hIgG) are now available to support this GU workflow
  • 29. ©2015 Waters Corporation 31 UNIFI ® Scientific Library for Automated GU or GU+Mass Glycan Confirmation Experimental GU value FLR label mass Waters Glycan GU Library: • Experimentally derived GU Retention (>10 injections/protein) • Data from proteins representing spectrum of glycan diversity • All entries confirmed with exoglycosidase digestion
  • 30. ©2015 Waters Corporation 32 UNIFI® Scientific Library for Confident Glycan Assignments
  • 31. ©2015 Waters Corporation 33 Powerful UNIFI® Reporting Architecture Simplifies Communication of Results Example
  • 32. ©2015 Waters Corporation 34 UNIFI® Glycan DDA Workflow
  • 33. ©2015 Waters Corporation 35 Optional UNIFI® Export to SimGlycan for MS/MS Database Search A2G2S1
  • 34. ©2015 Waters Corporation 36 Enhanced MS/MS with RapiFluor-MS™ Labeling FLR BPI MS MSMS MS performance extends to fragmentation data
  • 35. ©2015 Waters Corporation 37 Enhanced MSMS with RapiFluor-MS Labeling MS performance extends to MS/MS fragmentation data
  • 36. ©2015 Waters Corporation 38 Poster WCBP 2015 Poster P-115-T Developing a Scientific Library for UPLC/FLR/MS Analysis of Released N-glycans Labeled with a Novel Labeling Reagent Download pdf
  • 37. ©2015 Waters Corporation 39 RapiFluor-MS: Enhanced Workflows for Glycan Monitoring
  • 38. ©2015 Waters Corporation 40 30.0010.00 12.00 14.00 16.00 18.00 20.00 22.00 24.00 26.00 28.00 24.00 28.00 32.00 36.00 40.00 44.00 48.00 52.00 56.00 60.00 64.00 Alliance HPLC XBridge Glycan BEH Amide, 130Å, 2.5µm 3.0 X 225 mm total length (150 mm + 75 mm) Flow Rate: 0.56 mL/minute H-Class BIO UPLC ACQUITY UPLC Glycan BEH Amide, 130Å, 1.7µm 2.1 X 150 mm Flow Rate: 0.40 mL/minute Total Run Time = 55 minutes Total Run Time = 121.3 minutes Fluorescence(relative) Time (minutes)  Comparable sensitivity and resolution – 3x sample load / 2x increase in time  Transfer between labs with different LC equipment capabilities Transferability between UPLC® and HPLC RapiFluor-MS™ Labeled Glycans
  • 39. ©2015 Waters Corporation 41 Glycan Monitoring  ACQUITY UPLC® H-Class Bio System  ACQUITY UPLC Column Manager  ACQUITY UPLC FLR Detector  ACQUITY® QDa® Mass Detector  Empower® or MassLynx® Informatics  GlycoWorks™ RapiFluor-MS™ N-Glycan Kit  ACQUITY UPLC Glycan BEH Amide Column
  • 40. ©2015 Waters Corporation 42 ACQUITY® QDa® Mass Detector A breakthrough product with mass appeal  Revolutionary innovative design focused on ease of use for analysts  Empowering analytical chemists everywhere with orthogonal mass detection – added information with every sample  Compact, robust and affordable: Built for constant use with a wide variety of chromatographic conditions  Seamlessly integrates with Empower based HPLC & UPLC®
  • 41. ©2015 Waters Corporation 43 Automated Start Up Provides Robust, Reproducible Performance  Automated resolution and calibration occurs with each start-up ensuring mass information is accurate and precise  ESI interface optimized for UPLC® performance to ensure chromatographic resolution, sensitivity and throughput is preserved  Disposable sample aperature and capillary for easy maintenance Graphic QDa® monitor display enables easy viewing and adjustment of system parameters
  • 42. ©2015 Waters Corporation 44 Routine N-Glycan Detection with Comparable FLR and MS response Minutes 5 10 15 20 25 30 35 40 Minutes 5 10 15 20 25 30 35 40 Detection across a broad range of glycoforms: IgG Simple bi-antennery structures RNase B High mannose structures Fetuin Large, complex structures
  • 43. ©2015 Waters Corporation 45 IgG Glycan Profile and Structure Confirmation Using ACQUITY® QDa® Key take away: Large dynamic range – can clearly see most abundant and least abundant glycoforms. 0.00 240.00 480.00 Intensity 0.0 1.6x106 3.2x10 6 Minutes 10.00 15.00 20.00 25.00 30.00 896.0 Intensity 0.0 12000.0 24000.0 m/z 600 1200 A2G1b 0.5% RPA 888.2 Intensity 0 300000 600000 m/z 600 1200 FA2 20.5% RPA EU
  • 44. ©2015 Waters Corporation 46 Intuitive GMP compliant Reporting Empower® integration enables annotation of peaks with names and m/z A2-815.1 FA2-888.2 FA2B-989.6 A2G1a-896.2 A2G1b-896.0 FA2G1a-969.3 FA2G1b-969.2 FA2BG1a-1070.7 FA2BG1b-1070.6 A2G2-977.1 FA2G2-1050.3 FA2BG2-1151.8 FA2G1S1-1114.6 FA2G2S1-1196.0 FA2BG2S1-865.3 FA2G2S2-894.7 FA2BG2S2-962.2 0.00 240.00 480.00 Minutes 10.00 15.00 20.00 25.00 30.00 EU
  • 45. ©2015 Waters Corporation 47 Developing a Rapid Method for Glycan Analysis EU 0 10 20 30 40 Minutes 2 3 4 5 10 minute Method EU 0 10 20 Minutes 5 10 15 20 55 minute Method
  • 46. ©2015 Waters Corporation 48 Rapid Screening Process for Development Samples EU 0 20 40 FLR Intensity 0 1x106 2x106 Minutes 1 2 3 4 5 6 SIR Overlay Trastuzumab N-Glycan Analysis RapiFluor-MS™ labeled glycans: 10 minute method Intensity 0 50000 Intensity 0 200000 Intensity 0 1x10 6 2x10 6 Intensity 0 50000 100000 Intensity 0 1x10 6 Intensity 0 200000 400000 Intensity 0 20000 Minutes 1 2 3 4 5 6 A2G(4)1 895.9 m/z F(6)A2 887.9 m/z F(6)A2G(4)1 968.9 m/z F(6)A2G(4)2 1049.9 m/z A2 814.8 m/z F(6)A2G(4)2S1 1195.5 m/z M5 774.1 m/z
  • 47. ©2015 Waters Corporation 49 Monitoring Glycan Ratios Keeping Tabs on Mannose 5 Mannose 5 spiked in Low Medium High Inj 1 0.61 0.96 1.20 Inj 2 0.57 0.90 1.11 Inj 3 0.55 0.86 1.18 Mean 0.58 0.91 1.16 StDev 0.03 0.05 0.04 % RSD 5.44 5.47 3.85 Intensity 0 60000 120000 180000 240000 Minutes 2.00 2.50 3.00 3.50 4.00 Intensity 0.0 35000.0 70000.0 105000.0 140000.0 Minutes 2.00 2.50 3.00 3.50 4.00 F(6)A2G(4)1 SIR: 968.9 m/z M5 SIR: 774.1 m/z Man5: F(6)A2G(4)1 Ratio
  • 48. ©2015 Waters Corporation 50 Released N-Glycan UPLC Analysis Workflows SAMPLE PREP SEPARATION DETECTION & INFORMATICS GlycoWorks™ Kits RapiFluor-MS™ N-Glycan Kit ACQUITY® FLR/QDa and Empower® 3 Software FLR/Xevo® G2-XS QTof MS and UNIFI® Scientific Information System ACQUITY UPLC® Glycan BEH Amide Column Deglycosylation, Labeling and Clean-up in 30 min Unmatched sensitivity for FLR and MS detection FLR Quantification GU Retention MS Confirmation FLR Quantification GU Retention Accurate Mass Confirmation MS/MS Fragmentation FLR TIC MS/MS
  • 49. ©2015 Waters Corporation 51 Poster WCBP 2015 Poster P-206-W Routine Monitoring of N-Glycans Using a Novel Labeling Reagent with Fluorescence and Mass Detection Download pdf
  • 50. ©2015 Waters Corporation 52 RapiFluor-MS N-Glycan Labeling: A breakthrough technology for released glycan LC and MS analysis

Notas do Editor

  1. Based on the observed chromatographic peak areas, response factors for fluorescence and MS detection were determined. These results indicate that RapiFluor-MS labeled glycans produce 2x higher fluorescence signal and, more astoundingly, nearly 800x greater MS signal than N-glycans labeled with Instant AB.
  2. In this slide, deconvoluted mass spectra are presented for a mAb subjected to various conditions. The top spectrum shows the mAb before any treatment. The middle spectrum after treatment with only deglycosylation conditions. Lastly, the bottom spectrum after our combined approach of surfactant-based heat denaturation and Rapid PNGase F deglycosyaltion.