Characterization of lectin binding affinities via direct LC-MS profiling: implications for glycopeptide enrichment and separation strategies
Literature Information
Feifei Zhu, David E. Clemmer, Jonathan C. Trinidad
Determining the affinity between a lectin and its target glycans is an important goal, both for understanding the biological functions of a given lectin as well as enabling the use of that lectin for targeted enrichment of glycosylated species from complex samples. While the overall selectivities of many lectins have been characterized, such studies generally require individually purified lectins and glycans. From these analyses, it is clear that a given lectin does not bind all of its target glycans with the same affinity. Rather, lectins display a continuum of affinities for the range of glycan structures they may encounter. Because of this continuum, it is not straightforward in practice to determine which set of structures will be enriched using a lectin as an affinity reagent. Here we describe the development of glycan affinity chromatography coupled directly to electrospray mass spectrometry, which enables direct analysis of interactions of lectins with both glycans and glycoconjugates from complex mixtures. By observing the elution behavior of individual species, we are able to determine exactly which set of glycoconjugates would be enriched for a given lectin. Furthermore, this approach allows for the direct assessment of affinity constants between an individual lectin and a large number of glycans in a single experiment, which can be conducted using a complex mixture of unpurified glycans of varying concentrations.
Recommended Journals
Related Literature
Effects of water on the solvation and structure of lipase in deep eutectic solvents containing a protein destabilizer and stabilizer
Qi Qiao, Jian Shi, Qing Shao
DOI: 10.1039/D1CP03282H
Theoretical study of the dissociative photodetachment dynamics of the hydrated superoxide anion cluster
Yu Hashimoto, Kohei Saito, Toshiyuki Takayanagi, Hiroto Tachikawa
DOI: 10.1039/D1CP02379A
Zn–Fe–oxide nanostructures of different iron concentrations for multifunctional applications: properties and precursor influence
V. Mihalache, C. Negrila, I. Mercioniu, N. Iacob, V. Kuncser
DOI: 10.1039/D1CP01002F
Phase transitions in 1-bromoadamantane compared to 1-chloroadamantane: similarities and unique features
Igor V. Danilov, Elena L. Gromnitskaya, Vadim V. Brazhkin
DOI: 10.1039/D1CP03080A
Large Rashba splitting, carrier mobility, and valley polarization in a 1T-SnS2/MoTe2 heterostructure
Sukai Teng, Jia Li, Xiujuan Mao, Fuli He, Ze Liu, Jiaxi Wang, Yafan Wang
DOI: 10.1039/D1CP02039K
Polymer network formation mechanism of multifunctional poly(ethylene glycol)s in ionic liquid electrolyte with a lithium salt
Asumi Ishikawa, Namie Ikeda, Shuichi Maeda, Kenta Fujii
DOI: 10.1039/D1CP02710G
Chiral recognition via a stereodynamic vanadium probe using the electronic circular dichroism effect in differential Raman scattering
Davide Carraro, Giulia Licini, Petr Bouř, Cristiano Zonta
DOI: 10.1039/D1CP03020E
The Fermi level as an energy reference in liquid jet X-ray photoelectron spectroscopy studies of aqueous solutions
Lucía Pérez Ramírez, Anthony Boucly, Florent Saudrais, Emmanuel Maisonhaute, Aleksandar R. Milosavljević, Christophe Nicolas, François Rochet
DOI: 10.1039/D1CP01511G
Molecular dynamics study on the inhibition mechanisms of ReACp53 peptide for p53–R175H mutant aggregation
Jiangtao Lei, Mengqiang Cai, Yun Shen, Dongdong Lin, Xiaohua Deng
DOI: 10.1039/D1CP03094A
Single sheets of graphene for fabrication of fibers with enhanced mechanical properties
Muhammad G. Salim, Luke A. Thimons, Min A. Kim, Brennan Carr, Michelle Montgomery, Nathan Tolman, Tevis D. B. Jacobs, Haitao Liu
DOI: 10.1039/D1CP03238K
You might also like
What precautions should be taken when handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3)?
When handling 4-Methyl-6-(trifluoromethyl)quinoline (CAS: 40716-16-3), safety go...
What is 4-(3,5-Difluorophenyl)aniline (CAS: 405058-00-6)?
4-(3,5-Difluorophenyl)aniline is an aromatic organic compound with the CAS numbe...
How is 5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid (CAS: 338982-07-3) typically synthesized?
5-{[4-(Trifluoromethyl)phenyl]sulfanyl}-1,2,3-thiadiazole-4-carboxylic acid can ...
What is the market or research trend for 4-Benzylaniline hydrochloride (CAS: 6317-57-3)?
The market for 4-Benzylaniline hydrochloride (CAS: 6317-57-3) is steadily growin...
Is [3-(Diethylsulfamoyl)phenyl]boronic acid (CAS: 871329-58-7) safe?
[3-(Diethylsulfamoyl)phenyl]boronic acid is generally considered safe when handl...
What are the main uses of 3-Bromo-2,5-dimethoxyaniline (CAS: 115929-62-9)?
3-Bromo-2,5-dimethoxyaniline is mainly used in the pharmaceutical and chemical i...
What regulatory guidelines apply to N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7)?
N-Methyl-1-(5-methyl-1H-indol-3-yl)methanamine (CAS: 915922-67-7) is subject to ...
What industries use Carbamic acid, N-[(5S)-5,6-diamino-6-oxohexyl]-, 1,1-dimethylethyl ester (CAS: 24828-96-4)?
This compound is primarily used in the pharmaceutical industry for the synthesis...
How should 2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) be stored?
2-Methyl-2-propanyl [(1S,3R)-3-aminocyclohexyl]carbamate (CAS: 1298101-47-9) sho...
What industries use Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9)?
Ethyl 2-bromo-4,4,4-trifluorobutanoate (CAS: 367-33-9) is utilized in the pharma...
Source Journal
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.










![N-{3-[Benzyl(methyl)amino]propyl}-9-chloro-5,6,7,8-tetrahydro-2-acridinecarboxamide structure N-{3-[Benzyl(methyl)amino]propyl}-9-chloro-5,6,7,8-tetrahydro-2-acridinecarboxamide structure](https://static.chemtradehub.com/structs/142/1426944-49-1-1e4c.webp)
![Methyl 3-({2'-[(E)-(hydroxyhydrazono)methyl]-4-biphenylyl}methyl)-2-oxo-2,3-dihydro-1H-benzimidazole-4-carboxylate structure Methyl 3-({2'-[(E)-(hydroxyhydrazono)methyl]-4-biphenylyl}methyl)-2-oxo-2,3-dihydro-1H-benzimidazole-4-carboxylate structure](https://static.chemtradehub.com/structs/149/1499167-72-4-034a.webp)
![Imidazo[1,2-c]pyrimidine structure Imidazo[1,2-c]pyrimidine structure](https://static.chemtradehub.com/structs/274/274-78-2-8b4c.webp)

