Dosimetry determines the initial OH radical concentration in fast photochemical oxidation of proteins (FPOP) - Wikidata - awgldk - TriplyDB

Dosimetry determines the initial OH radical concentration in fast photochemical oxidation of proteins (FPOP)

Dosimetry determines the initial OH radical concentration in fast photochemical oxidation of proteins (FPOP)

http://www.wikidata.org/entity/Q35567269

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Hydroxyl Radical Dosimetry for High Flux Hydroxyl Radical Protein Footprinting Applications Using a Simple Optical Detection Method.Probing the Time Scale of FPOP (Fast Photochemical Oxidation of Proteins): Radical Reactions Extend Over Tens of Milliseconds.Fast Photochemical Oxidation of Proteins Maps the Topology of Intrinsic Membrane Proteins: Light-Harvesting Complex 2 in a Nanodisc.Quantitative Protein Topography Measurements by High Resolution Hydroxyl Radical Protein Footprinting Enable Accurate Molecular Model Selection Incorporation of a Reporter Peptide in FPOP Compensates for Adventitious Scavengers and Permits Time-Dependent Measurements.Laser-Initiated Radical Trifluoromethylation of Peptides and Proteins: Application to Mass-Spectrometry-Based Protein Footprinting.Mass Spectrometry-Based Fast Photochemical Oxidation of Proteins (FPOP) for Higher Order Structure Characterization.Modifications generated by fast photochemical oxidation of proteins reflect the native conformations of proteins.Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

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P2860

Dosimetry determines the initial OH radical concentration in fast photochemical oxidation of proteins (FPOP)

http://www.wikidata.org/entity/Q35567269

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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Dosimetry determines the initi ...... l oxidation of proteins (FPOP)

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Journal of the American Society for Mass Spectrometry

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Dosimetry determines the initi ...... l oxidation of proteins (FPOP)

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Daryl Giblin

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Don L Rempel

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Hao Zhang

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Michael L Gross

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P2860

Mass spectrometry-based proteomics

Laser flash photolysis of hydrogen peroxide to oxidize protein solvent-accessible residues on the microsecond timescale.

Fast events in protein folding: relaxation dynamics and structure of the I form of apomyoglobin.

Fast photochemical oxidation of protein footprints faster than protein unfolding.

Fast photochemical oxidation of proteins for comparing structures of protein-ligand complexes: the calmodulin-peptide model system.

Millisecond radiolytic modification of peptides by synchrotron X-rays identified by mass spectrometry.

Sulfate radical anion as a new reagent for fast photochemical oxidation of proteins.

Fast photochemical oxidation of proteins and mass spectrometry follow submillisecond protein folding at the amino-acid level.

Fast photochemical oxidation of proteins for epitope mapping

New protein footprinting: fast photochemical iodination combined with top-down and bottom-up mass spectrometry.

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