No full text
Poster (Scientific congresses and symposiums)
Minimizing the peptide/protein loss due to interactions with custom consumable materials for proteomic study of protein samples at very low concentrations
Kune, Christopher; Fleron, Maximilien; Baiwir, Dominique et al.
2022Next-Generation Protein Analysis and Detection (NGPAD), 4th edition
Peer reviewed
 

Files


Full Text
No document available.

Send to



Details



Keywords :
Peptide surface interaction; low-affinity vial; Sample preparation; Downscaling proteomics; Single-cell proteomics
Abstract :
[en] Liquid chromatography-mass spectrometry (LC-MS) proteomics is challenged by the detection limit of current mass analyzers for low concentration – low quantity samples (e.g., single cell proteomics and tissue microdissection proteomics) but also especially by material losses during sample preparation steps. The binding of peptides and proteins to the surfaces of consumables significantly reduces the effective concentration in the solution, which further drastically decreases proteomic performance when the concentration of the starting material decreases. In addition to the optimization of the experimental protocols for the preparation of the samples and the technical evolution of the mass analyzers, the nature of the polymeric surface of consumables is crucial. We have therefore designed microvials suitable for proteomic low concentration sample preparation that can be molded in different polymeric materials. A comparative study has shown that the nature of the polymer material has a strong influence on proteomic performances for low concentration samples ranging from 1.5 to 10 ng/µl of proteins (injected quantity is less than 10ng). The nature of the vial has less impact on protein concentrations above 10ng/µl. Peptide loss due to surface interaction is not homogeneous with respect to peptide hydrophobicity, hydrophobic peptides being more impacted on commonly used vials. A polar polymer surface should therefore reduce hydrophobic interactions with peptides. Some polymer materials show promising behaviors for low concentration to single cell proteomic samples, leading to a 20% increase in identification compared to commercially available vials commonly used for proteomics.
Research center :
MolSys - Molecular Systems - ULiège
Disciplines :
Chemistry
Author, co-author :
Kune, Christopher  ;  Université de Liège - ULiège > Molecular Systems (MolSys)
Fleron, Maximilien ;  Université de Liège - ULiège > GIGA > GIGA Platforms
Baiwir, Dominique  ;  Université de Liège - ULiège > GIGA > GIGA Platforms
Vandormael, Denis;  Sirris, Liège, BE
Gilet, Tristan  ;  Université de Liège - ULiège > Département d'aérospatiale et mécanique > Microfluidique
Nguyen, Laurent  ;  Université de Liège - ULiège > GIGA > GIGA Stem Cells - Molecular Regulation of Neurogenesis
Eppe, Gauthier  ;  Université de Liège - ULiège > Molecular Systems (MolSys)
Mazzucchelli, Gabriel  ;  Université de Liège - ULiège > Molecular Systems (MolSys)
Language :
English
Title :
Minimizing the peptide/protein loss due to interactions with custom consumable materials for proteomic study of protein samples at very low concentrations
Publication date :
30 May 2022
Event name :
Next-Generation Protein Analysis and Detection (NGPAD), 4th edition
Event place :
Ghent, Belgium
Event date :
30-31 Mai 2022
Audience :
International
Peer reviewed :
Peer reviewed
Name of the research project :
ChipOmics (Win2WAL)
Funders :
Région wallonne [BE]
Funding number :
2010126
Available on ORBi :
since 05 July 2022

Statistics


Number of views
90 (10 by ULiège)
Number of downloads
0 (0 by ULiège)

Bibliography


Similar publications



Contact ORBi