scholarly journals Linkage Memory in Underivatized Protonated Carbohydrates

Author(s):  
Abhigya Mookherjee ◽  
Sanjit S. Uppal ◽  
Taylor A. Murphree ◽  
Miklos Guttman

<p>Carbohydrates are among the most complex class of biomolecules and even subtle variations in their structures are attributed to diverse biological function. Mass spectrometry has been essential for large scale glycomics and glycoproteomics studies, but the gas-phase structures and sometimes anomalous fragmentation properties of carbohydrates present longstanding challenges. Here we investigate the gas-phase properties of a panel of isomeric protonated disaccharides differing in their linkage configurations. Multiple conformations were evident for most of the structures based on their fragment ion abundances by tandem mass spectrometry, their ion mobilities in several gases, and their deuterium uptake kinetics by gas-phase hydrogen deuterium exchange. Most notably, we find that the properties of the Y-ion fragments are characteristically influenced by the precursor carbohydrate’s linkage configuration. This study reveals how protonated carbohydrate fragment ions can retain ‘linkage memory’ that provides structural insight into their intact precursor.</p>

2020 ◽  
Author(s):  
Abhigya Mookherjee ◽  
Sanjit S. Uppal ◽  
Taylor A. Murphree ◽  
Miklos Guttman

<p>Carbohydrates are among the most complex class of biomolecules and even subtle variations in their structures are attributed to diverse biological function. Mass spectrometry has been essential for large scale glycomics and glycoproteomics studies, but the gas-phase structures and sometimes anomalous fragmentation properties of carbohydrates present longstanding challenges. Here we investigate the gas-phase properties of a panel of isomeric protonated disaccharides differing in their linkage configurations. Multiple conformations were evident for most of the structures based on their fragment ion abundances by tandem mass spectrometry, their ion mobilities in several gases, and their deuterium uptake kinetics by gas-phase hydrogen deuterium exchange. Most notably, we find that the properties of the Y-ion fragments are characteristically influenced by the precursor carbohydrate’s linkage configuration. This study reveals how protonated carbohydrate fragment ions can retain ‘linkage memory’ that provides structural insight into their intact precursor.</p>


2005 ◽  
Vol 83 (11) ◽  
pp. 1953-1960 ◽  
Author(s):  
Belal M Hossain ◽  
Douglas A Simmons ◽  
Lars Konermann

Electrospray ionization (ESI) mass spectrometry (MS) has become a popular tool for monitoring ligand–protein and protein–protein interactions. Due to the "gentle" nature of the ionization process, it is often possible to transfer weakly bound complexes into the gas phase, thus making them amenable to MS detection. One problem with this technique is the potential occurrence of fragmentation events during ESI. Also, some analytes tend to cluster together during ionization, thus forming nonspecific gas-phase assemblies that do not represent solution-phase complexes. In this work, we implemented a hydrogen–deuterium exchange (HDX) approach that can reveal whether or not the free and (or) bound constituents of a complex observed in ESI-MS reflect the binding situation in solution. Proteins are subjected to ESI immediately following an isotopic labeling pulse; only ligand-free and ligand-bound protein ions that were formed directly from the corresponding solution-phase species showed different HDX levels. Using myoglobin as a model system, it is demonstrated that this approach can readily distinguish scenarios where the heme–protein interactions were disrupted in solution from those where dissociation of the complex occurred in the gas phase. Experiments on cytochrome c strongly suggest that dimeric protein ions observed in ESI-MS reflect aggregates that were formed in solution.Key words: electrospray mass spectrometry, ligand–protein interaction, noncovalent complex, hydrogen–deuterium exchange, protein folding.


2020 ◽  
Vol 92 (11) ◽  
pp. 7725-7732 ◽  
Author(s):  
Sanjit S. Uppal ◽  
Abhigya Mookherjee ◽  
Rick Harkewicz ◽  
Sarah E. Beasley ◽  
Matthew F. Bush ◽  
...  

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