Preparation of miniaturized hydrophilic affinity monoliths: Towards a reduction of non-specific interactions and an increased target protein density

被引:11
作者
Gil, Julie [1 ]
Krimm, Isabelle [2 ]
Dugas, Vincent [1 ]
Demesmay, Claire [1 ]
机构
[1] Univ Claude Bernard Lyon 1, Univ Lyon, CNRS, Inst Sci Analyt,UMR 5280, 5 Rue Doua, F-69100 Villeurbanne, France
[2] Univ Claude Bernard Lyon 1, Univ Lyon, INSERM 1052, Small Mol Biol Targets Team,Ctr Rech Cancerol Lyon, F-69373 Lyon, France
关键词
Frontal affinity chromatography; Hydrophilic organic monolith; Non-specific interactions; Fragment screening; SAMPLE PREPARATION; IN-LINE; CHROMATOGRAPHY; PRINCIPLES; COLUMN; WATER;
D O I
10.1016/j.chroma.2022.463670
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In affinity chromatography, non-specific interactions between the ligands and the affinity column may af-fect the results, leading to misinterpretations during the investigation of protein-ligand interactions (de-tection of false positives in ligand screening, lack of specificity in purification). Such non-specific inter-actions may arise both from the underlying support or from the target protein itself. If the second ones are protein-dependent (and cannot be studied in a general framework), the first ones occur in the same way regardless of the immobilized target. We propose a methodology to identify the origin of such non-specific interactions with the underlying material of the affinity column. This methodology relies on the systematic investigation of the retention behavior of a set of 41 low-molecular weight compounds cover-ing a wide chemical space (net charge, log D, functionality). We first demonstrate that the main source of non-specific interactions on the most commonly used GMA-co-EDMA monolith comes from hydrophobic effects. To reduce such non-specific interactions, we developed a new hydrophilic glycidyl methacrylate-based monolith by replacing the EDMA crosslinker by the more hydrophilic N -N' Methylenebisacrylamide (MBA). Optimization of the synthesis parameters (monomer content, initiation type, temperature) has fo-cused on the reduction of non-specific interaction with the monolithic support while maximizing the amount of protein that can be grafted onto the monolith at the issue of its synthesis. The retention data of the 41 test solutes on the new poly(GMA-co-MBA) monolith shows a drastic reduction of non-specific interactions except for cationic compounds. The particular behavior of cationic compounds is due to their electrostatic interactions with carboxylic groups resulting from the partial acidic hydrolysis of amide groups of MBA during the epoxide ring opening step. So, the ring opening step in acidic media was replaced by a hot water treatment to avoid side reaction on MBA. The new monolith poly(GMA-co-MBA) not only has improved hydrophilic surface properties but also a higher protein density (16 +/- 0.8 pmol cm -1 instead of 8 +/- 0.3 pmol cm -1). To highlight the benefits of this new hydrophilic monolith for affinity chromatographic studies, frontal affinity chromatography experiments were conducted on these monoliths grafted with con A.(c) 2022 Elsevier B.V. All rights reserved.
引用
收藏
页数:9
相关论文
共 27 条
[11]   Frontal affinity chromatography: A unique research tool for biospecific interaction that promotes glycobiology [J].
Kasai, Kenichi .
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 2014, 90 (07) :215-234
[12]   Postpolymerization modification of a hydroxy monolith precursor. Part III. Activation of poly(hydroxyethyl methacrylate-co-pentaerythritol triacrylate) monolith with epoxy functionalities followed by bonding of glycerol, polyamines, and hydroxypropyl-β-cyclodextrin for hydrophilic interaction and chiral capillary electrochromatography [J].
Khadka, Shantipriya ;
El Rassi, Ziad .
ELECTROPHORESIS, 2016, 37 (23-24) :3178-3185
[13]   Miniaturized weak affinity chromatography for ligand identification of nanodiscs-embedded G-protein coupled receptors [J].
Lecas, Lucile ;
Hartmann, Lucie ;
Caro, Lydia ;
Mohamed-Bouteben, Sarah ;
Raingeval, Claire ;
Krimm, Isabelle ;
Wagner, Renaud ;
Dugas, Vincent ;
Demesmay, Claire .
ANALYTICA CHIMICA ACTA, 2020, 1113 :26-35
[14]   Monolith weak affinity chromatography for μg-protein-ligand interaction study [J].
Lecas, Lucile ;
Randon, Jerome ;
Berthod, Alain ;
Dugas, Vincent ;
Demesmay, Claire .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2019, 166 :164-173
[15]   Affinity monolith chromatography: A review of general principles and applications [J].
Li, Zhao ;
Rodriguez, Elliott ;
Azaria, Shiden ;
Pekarek, Allegra ;
Hage, David S. .
ELECTROPHORESIS, 2017, 38 (22-23) :2837-2850
[16]   Affinity monolith chromatography [J].
Mallik, Rangan ;
Hage, David S. .
JOURNAL OF SEPARATION SCIENCE, 2006, 29 (12) :1686-1704
[17]   Porous monoliths for on-line sample preparation: A review [J].
Masini, Jorge C. ;
Svec, Frantisek .
ANALYTICA CHIMICA ACTA, 2017, 964 :24-44
[18]   Current trends in the development of polymer-based monolithic stationary phases [J].
Nechvatalova, Martina ;
Urban, Jiri .
ANALYTICAL SCIENCE ADVANCES, 2022, 3 (3-4) :154-164
[19]   STUDIES ON THE SPECIFIC INTERACTION OF CONCANAVALIN-A AND SACCHARIDES BY AFFINITY-CHROMATOGRAPHY - APPLICATION OF QUANTITATIVE AFFINITY-CHROMATOGRAPHY TO A MULTIVALENT SYSTEM [J].
ODA, Y ;
KASAI, K ;
ISHII, S .
JOURNAL OF BIOCHEMISTRY, 1981, 89 (01) :285-296
[20]   Affinity monolith chromatography: a review of principles and recent analytical applications [J].
Pfaunmiller, Erika L. ;
Paulemond, Marie Laura ;
Dupper, Courtney M. ;
Hage, David S. .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2013, 405 (07) :2133-2145