Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

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Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

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im September 2018 veröffentlichter wissenschaftlicher Artikel

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scientific article published on 25 June 2018

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wetenschappelijk artikel

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наукова стаття, опублікована у вересні 2018

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Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

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Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

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Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

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Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

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Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

@en

Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

@nl

P1476

Variation in FPOP Measurements Is Primarily Caused by Poor Peptide Signal Intensity

@en

P2093

Charles K Mobley

http://www.w3.org/2001/XMLSchema#string

Joshua S Sharp

http://www.w3.org/2001/XMLSchema#string

Lindsey Miller

http://www.w3.org/2001/XMLSchema#string

Niloofar Abolhasani Khaje

http://www.w3.org/2001/XMLSchema#string

Sandeep K Misra

http://www.w3.org/2001/XMLSchema#string

Zixuan Li

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P2860

Quantitative protein topography analysis and high-resolution structure prediction using hydroxyl radical labeling and tandem-ion mass spectrometry (MS)

Pulsed electron beam water radiolysis for submicrosecond hydroxyl radical protein footprinting

Aliphatic peptidyl hydroperoxides as a source of secondary oxidation in hydroxyl radical protein footprinting.

Hydroxyl Radical Dosimetry for High Flux Hydroxyl Radical Protein Footprinting Applications Using a Simple Optical Detection Method.

Fast photochemical oxidation of proteins for comparing solvent-accessibility changes accompanying protein folding: data processing and application to barstar

Nanosecond laser-induced photochemical oxidation method for protein surface mapping with mass spectrometry.

Quantifying protein interface footprinting by hydroxyl radical oxidation and molecular dynamics simulation: application to galectin-1.

Fast photochemical oxidation of protein footprints faster than protein unfolding.

Cold chemical oxidation of proteins.

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

P2888

s13361-018-1994-y

P304

1901-1907

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P31

scholarly article

P356

10.1007/S13361-018-1994-Y

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Evgeny Nudler

P577

2018-06-25T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29943081

http://www.w3.org/2001/XMLSchema#string

P921

structural biology

P932

6087495

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