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Travelling-wave ion mobility and negative ion fragmentation of high-mannose N-glycans

Travelling-wave ion mobility and negative ion fragmentation of high-mannose N-glycans
Travelling-wave ion mobility and negative ion fragmentation of high-mannose N-glycans

The isomeric structure of high-mannose N-glycans can significantly impact biological recognition events. Here, the utility of travelling-wave ion mobility mass spectrometry for isomer separation of high-mannose N-glycans is investigated. Negative ion fragmentation using collision-induced dissociation gave more informative spectra than positive ion spectra with mass-different fragment ions characterizing many of the isomers. Isomer separation by ion mobility in both ionization modes was generally limited, with the arrival time distributions (ATD) often showing little sign of isomers. However, isomers could be partially resolved by plotting extracted fragment ATDs of the diagnostic fragment ions from the negative ion spectra, and the fragmentation spectra of the isomers could be extracted by using ions from limited areas of the ATD peak. In some cases, asymmetric ATDs were observed, but no isomers could be detected by fragmentation. In these cases, it was assumed that conformers or anomers were being separated. Collision cross sections of the isomers in positive and negative fragmentation mode were estimated from travelling-wave ion mobility mass spectrometry data using dextran glycans as calibrant. More complete collision cross section data were achieved in negative ion mode by utilizing the diagnostic fragment ions. Examples of isomer separations are shown for N-glycans released from the well-characterized glycoproteins chicken ovalbumin, porcine thyroglobulin and gp120 from the human immunodeficiency virus. In addition to the cross-sectional data, details of the negative ion collision-induced dissociation spectra of all resolved isomers are discussed.

fragmentation, high mannose, isomers, N-linked glycosylation, T-wave ion mobility
1076-5174
219-235
Harvey, David J.
8bb24417-3852-4b1f-827b-0d5d2c176744
Scarff, Charlotte A.
7b7a0970-d9c0-4c8a-90bc-150616a6f071
Edgeworth, Matthew
c5c55ff2-e3a7-4237-baa2-079b0001b688
Struwe, Weston B.
16a348b1-3921-4a2d-b5fb-d341fccea65f
Pagel, Kevin
4922aa27-38fc-45d8-9e30-eae9799b874d
Thalassinos, Konstantinos
75b3f786-6a27-420a-8727-97eafb34c022
Crispin, Max
cd980957-0943-4b89-b2b2-710f01f33bc9
Scrivens, Jim
12019574-e300-490b-8a96-50fa927bfd89
Harvey, David J.
8bb24417-3852-4b1f-827b-0d5d2c176744
Scarff, Charlotte A.
7b7a0970-d9c0-4c8a-90bc-150616a6f071
Edgeworth, Matthew
c5c55ff2-e3a7-4237-baa2-079b0001b688
Struwe, Weston B.
16a348b1-3921-4a2d-b5fb-d341fccea65f
Pagel, Kevin
4922aa27-38fc-45d8-9e30-eae9799b874d
Thalassinos, Konstantinos
75b3f786-6a27-420a-8727-97eafb34c022
Crispin, Max
cd980957-0943-4b89-b2b2-710f01f33bc9
Scrivens, Jim
12019574-e300-490b-8a96-50fa927bfd89

Harvey, David J., Scarff, Charlotte A., Edgeworth, Matthew, Struwe, Weston B., Pagel, Kevin, Thalassinos, Konstantinos, Crispin, Max and Scrivens, Jim (2016) Travelling-wave ion mobility and negative ion fragmentation of high-mannose N-glycans. Journal of Mass Spectrometry, 51 (3), 219-235. (doi:10.1002/jms.3738).

Record type: Article

Abstract

The isomeric structure of high-mannose N-glycans can significantly impact biological recognition events. Here, the utility of travelling-wave ion mobility mass spectrometry for isomer separation of high-mannose N-glycans is investigated. Negative ion fragmentation using collision-induced dissociation gave more informative spectra than positive ion spectra with mass-different fragment ions characterizing many of the isomers. Isomer separation by ion mobility in both ionization modes was generally limited, with the arrival time distributions (ATD) often showing little sign of isomers. However, isomers could be partially resolved by plotting extracted fragment ATDs of the diagnostic fragment ions from the negative ion spectra, and the fragmentation spectra of the isomers could be extracted by using ions from limited areas of the ATD peak. In some cases, asymmetric ATDs were observed, but no isomers could be detected by fragmentation. In these cases, it was assumed that conformers or anomers were being separated. Collision cross sections of the isomers in positive and negative fragmentation mode were estimated from travelling-wave ion mobility mass spectrometry data using dextran glycans as calibrant. More complete collision cross section data were achieved in negative ion mode by utilizing the diagnostic fragment ions. Examples of isomer separations are shown for N-glycans released from the well-characterized glycoproteins chicken ovalbumin, porcine thyroglobulin and gp120 from the human immunodeficiency virus. In addition to the cross-sectional data, details of the negative ion collision-induced dissociation spectra of all resolved isomers are discussed.

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More information

Accepted/In Press date: 2 December 2015
e-pub ahead of print date: 4 March 2016
Published date: March 2016
Keywords: fragmentation, high mannose, isomers, N-linked glycosylation, T-wave ion mobility

Identifiers

Local EPrints ID: 414324
URI: http://eprints.soton.ac.uk/id/eprint/414324
ISSN: 1076-5174
PURE UUID: 2005e686-950d-4e42-8280-19abe354d7a8
ORCID for Max Crispin: ORCID iD orcid.org/0000-0002-1072-2694

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Date deposited: 26 Sep 2017 16:30
Last modified: 16 Mar 2024 04:30

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Contributors

Author: David J. Harvey
Author: Charlotte A. Scarff
Author: Matthew Edgeworth
Author: Weston B. Struwe
Author: Kevin Pagel
Author: Konstantinos Thalassinos
Author: Max Crispin ORCID iD
Author: Jim Scrivens

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