TY - JOUR
T1 - Standards-Free Absolute Quantitation of Oxidizable Glycopeptides by Coulometric Mass Spectrometry
AU - Chiu, Kai Yuan
AU - Ai, Yongling
AU - Tanim-AI Hassan, Md
AU - Li, Xuanwen
AU - Gunawardena, Harsha P.
AU - Chen, Hao
N1 - Publisher Copyright:
© 2024 American Society for Mass Spectrometry. Published by American Chemical Society. All rights reserved.
PY - 2024/7/3
Y1 - 2024/7/3
N2 - Currently, glycopeptide quantitation is mainly based on relative quantitation due to absolute quantitation requiring isotope-labeled or standard glycopeptides which may not be commercially available or are very costly and time consuming to synthesize. To address this grand challenge, coulometric mass spectrometry (CMS), based on the combination of electrochemistry (EC) and mass spectrometry (MS), was utilized to quantify electrochemically active glycopeptides without the need of using standard materials. In this study, we studied tyrosine-containing glycopeptides, NYIVGQPSS(β-GlcNAc)TGNL-OH and NYSVPSS(β-GlcNAc)TGNL-OH, and successfully quantified them directly with CMS with a discrepancy of less than 5% between the CMS measured amount and the theoretical amount. Taking one step further, we applied this approach to quantify glycopeptides generated from the digestion of NIST mAb, a monoclonal antibody reference material. Through HILIC column separation, five N297 glycopeptides resulting from NIST mAb tryptic digestion were successfully separated and quantified by CMS for an absolute amount without the use of any standard materials. This study indicates the potential utility of CMS for quantitative proteomics research.
AB - Currently, glycopeptide quantitation is mainly based on relative quantitation due to absolute quantitation requiring isotope-labeled or standard glycopeptides which may not be commercially available or are very costly and time consuming to synthesize. To address this grand challenge, coulometric mass spectrometry (CMS), based on the combination of electrochemistry (EC) and mass spectrometry (MS), was utilized to quantify electrochemically active glycopeptides without the need of using standard materials. In this study, we studied tyrosine-containing glycopeptides, NYIVGQPSS(β-GlcNAc)TGNL-OH and NYSVPSS(β-GlcNAc)TGNL-OH, and successfully quantified them directly with CMS with a discrepancy of less than 5% between the CMS measured amount and the theoretical amount. Taking one step further, we applied this approach to quantify glycopeptides generated from the digestion of NIST mAb, a monoclonal antibody reference material. Through HILIC column separation, five N297 glycopeptides resulting from NIST mAb tryptic digestion were successfully separated and quantified by CMS for an absolute amount without the use of any standard materials. This study indicates the potential utility of CMS for quantitative proteomics research.
KW - absolute quantitation
KW - antibody
KW - electrochemistry
KW - glycopeptide
KW - mass spectrometry
UR - http://www.scopus.com/inward/record.url?scp=85195026339&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85195026339&partnerID=8YFLogxK
U2 - 10.1021/jasms.4c00052
DO - 10.1021/jasms.4c00052
M3 - Article
C2 - 38815255
AN - SCOPUS:85195026339
SN - 1044-0305
VL - 35
SP - 1441
EP - 1450
JO - Journal of the American Society for Mass Spectrometry
JF - Journal of the American Society for Mass Spectrometry
IS - 7
ER -