English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  It is all about the solvent : on the importance of the mobile phase for ZIC-HILIC glycopeptide enrichment

Alagesan, K., Khilji, S. K., & Kolarich, D. (2017). It is all about the solvent: on the importance of the mobile phase for ZIC-HILIC glycopeptide enrichment. Analytical and Bioanalytical Chemistry, 409(2), 529-538. doi:10.1007/s00216-016-0051-6.

Item is

Files

show Files
hide Files
:
article (publisher version).pdf (Publisher version), 2MB
Name:
article (publisher version).pdf
Description:
-
OA-Status:
Visibility:
Public
MIME-Type / Checksum:
application/pdf / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
:
2368678_supp1.pdf (Supplementary material), 3MB
Name:
2368678_supp1.pdf
Description:
-
OA-Status:
Visibility:
Public
MIME-Type / Checksum:
application/pdf / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
License:
-
:
2368678_supp2.pdf (Supplementary material), 3MB
Name:
2368678_supp2.pdf
Description:
-
OA-Status:
Visibility:
Public
MIME-Type / Checksum:
application/pdf / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
License:
-

Locators

show

Creators

show
hide
 Creators:
Alagesan, Kathirvel1, Author           
Khilji, Sana K.2, Author           
Kolarich, Daniel1, Author           
Affiliations:
1Daniel Kolarich, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863301              
2Oren Moscovitz, Biomolekulare Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_3176803              

Content

show
hide
Free keywords: Open Access
 Abstract: Glycopeptide enrichment is a crucial step in glycoproteomics for which hydrophilic interaction chromatography (HILIC) has extensively been applied due to its low bias towards different glycan types. A systematic evaluation of applicable HILIC mobile phases on glycopeptide enrichment efficiency and selectivity is, to date, however, still lacking. Here, we present a novel, simplified technique for HILIC enrichment termed “Drop-HILIC”, which was applied to systematically evaluate the mobile phase effect on ZIC-HILIC (zwitterionic type of hydrophilic interaction chromatography) glycopeptide enrichment. The four most commonly used MS compatible organic solvents were investigated: (i) acetonitrile, (ii) methanol, (iii) ethanol and (iv) isopropanol. Glycopeptide enrichment efficiencies were evaluated for each solvent system using samples of increasing complexity ranging from well-defined synthetic glycopeptides spiked into different concentrations of tryptic BSA peptides, followed by standard glycoproteins, and a complex sample derived from human (depleted and non-depleted) serum. ZIC-HILIC glycopeptide efficiency largely relied upon the used solvent. Different organic mobile phases enriched distinct glycopeptide subsets in a peptide backbone hydrophilicity-dependant manner. Acetonitrile provided the best compromise for the retention of both hydrophilic and hydrophobic glycopeptides, whereas methanol was confirmed to be unsuitable for this purpose. The enrichment efficiency of ethanol and isopropanol towards highly hydrophobic glycopeptides was compromised as considerable co-enrichment of unmodified peptides occurred, though for some hydrophobic glycopeptides isopropanol showed the best enrichment properties. This study shows that even minor differences in the peptide backbone and solvent do significantly influence HILIC glycopeptide enrichment and need to be carefully considered when employed for glycopeptide enrichment.

Details

show
hide
Language(s):
 Dates: 2016-12-012017
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1007/s00216-016-0051-6
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Analytical and Bioanalytical Chemistry
  Abbreviation : Anal. Bioanal. Chem.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Berlin, Heidelberg : Springer
Pages: - Volume / Issue: 409 (2) Sequence Number: - Start / End Page: 529 - 538 Identifier: ISSN: 1618-2642

Source 2

show
hide
Title: Glycomics, Glycoproteomics and Allied Topics
Source Genre: Issue
 Creator(s):
Mechref, Yehia, Editor
Muddiman, David, Editor
Affiliations:
-
Publ. Info: -
Pages: - Volume / Issue: 409 (2) Sequence Number: - Start / End Page: 529 - 538 Identifier: ISSN: 1618-2642
ISSN: 1618-2650 (Online)