In-ESI H/D exchange is a convenient technique for analyzing small-molecular complex mixtures. However, such experiments do not yield sufficient levels of exchange or require an elevated temperature of the ion transfer capillary. Increased temperature may result in unexpected additional exchanges of -CH groups that may complicate the interpretation of the H/D exchange data used for identification. Gas-phase H/D exchange depends on the gas-phase basicity of the deuterating agent. In-ESI exchange involves both droplet-phase and gas-phase mechanisms, depending on a particular ion source setup and the deuterating agent used. Therefore, the addition of strong bases to the reaction mixture should facilitate in-ESI exchange. This work aimed to investigate the capabilities of different amines to improve in-ESI H/D exchange compared with pure DO and to choose an amine modifier to increase the extent of H/D exchange. It was shown that such additives substantially enhanced the extent of H/D exchange in small molecules, peptides, and proteins even without heating the capillary. It was found that the extent of exchange increases in the following order: tertiary amines < secondary amines < primary amines. Therefore, we suggest that amines act as deuterating agents after being exchanged with DO. These findings may improve H/D exchange applications, especially in small molecule analysis. The observation of improved H/D exchange with amine additives in peptides and proteins may become a subject of future research.
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http://dx.doi.org/10.1039/d2an00081d | DOI Listing |
J Am Soc Mass Spectrom
January 2025
Department of Medicinal Chemistry, University of Washington, Seattle, Washington 98195, United States.
An inherent strength of hydrogen/deuterium exchange coupled to mass spectrometry (HDX-MS) is its ability to detect the presence of multiple conformational states of a protein, which often manifest as multimodal isotopic envelopes. However, the statistical considerations for accurate analysis of multimodal spectra have yet to be established. Here we outline an unrestrained binomial distribution fitting approach with the corresponding statistical tests to accurately detect and, when possible, deconvolute isotopic distributions that contain multiple subpopulations.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States.
A Pt(II) aqua complex supported by mesoporous silica nanoparticle (MSN)-immobilized sulfonated CNN pincer ligand featuring a rigid SiO tether was prepared. This hybrid material was tested as a catalyst in H/D exchange reactions of C(sp)-H bonds of selected aromatic substrates and DO-2,2,2-trifluoroethanol- (TFE-) mixtures or CDCOD acting as a source of exchangeable deuterium. The catalyst immobilization served as a means to not only enable the catalyst's recyclability but also minimize the coordination of sulfonate groups and the metal centers originating from different catalyst's moieties that would preserve reactive Pt(OH) fragments needed for catalytic C-H bond activation.
View Article and Find Full Text PDFChemphyschem
January 2025
Institute of Physical and Theoretical Chemistry, Goethe University Frankfurt am Main, Max-von-Laue-Straße 7, 60438, Frankfurt, Germany.
The light-sensing activity of phytochromes is based on the reversible light-induced switching between two isomerization states of the bilin chromophore. These photo-transformations may not necessarily be only unidirectional, but could potentially branch back to the initial ground state in a thermally driven process termed shunt. Such shunts have been rarely reported, and thus our understanding of this process and its governing factors are limited.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Physical Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99352, USA.
The reaction coefficient for hydrogen/deuterium (H/D) exchange and the diffusion of hydrated excess protons within amorphous solid water (ASW) are characterized as a function of temperature. For these experiments, water films are deposited on a Pt(111) substrate at 108 K, and reactions with pre-adsorbed hydrogen atoms produce hydrated protons. Upon heating, protons diffuse within the water, and H/D exchange occurs when they encounter D2O probe molecules deposited in the films.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Department of chemistry, University of California, Riverside, Riverside, CA, 92521, USA.
Sulfated zirconium oxide (SZO) catalyzes the hydrogenolysis of isotactic polypropylene (iPP, M=13.3 kDa, Đ=2.4,
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