Literature DB >> 20669999

Laminar flow effects during laser-induced oxidative labeling for protein structural studies by mass spectrometry.

Lars Konermann1, Bradley B Stocks, Tomasz Czarny.   

Abstract

Laser-induced oxidative labeling of proteins provides insights into biomolecular structures and interactions. In these experiments, the hydroxyl radical ((*)OH) formed by photolysis of H(2)O(2) generates covalent modifications that are detectable by mass spectrometry. Under conditions where individual protein molecules are irradiated only once, the short (*)OH lifetime (approximately 1 micros) ensures that covalent modifications are formed before any oxidation-induced conformational changes take place. This feature implies that the method should be free of structural artifacts. It has been proposed that single-exposure conditions can be achieved by passing the solution through a capillary where successive laser pulses generate a string of irradiated flow segments that are well separated from one another. The current work explores the convection phenomena within the labeling capillary in more detail. The experiments are conducted at Reynolds numbers <<2000, resulting in laminar flow. The associated parabolic velocity profile causes a portion of each irradiated segment to remain in the labeling window during the subsequent laser pulse. Achieving a genuine single-exposure regime is, therefore, not possible. We estimate the fraction of labeled protein formed under laminar flow conditions, as well as the occurrence of multiple exposure events for any combination of experimental parameters (laser spot width, pulse frequency, and solution flow rate). A proper choice of these parameters provides extensive labeling, while keeping multiple exposure events at an acceptably low level. The theoretical framework developed here is supported by experimental data. Overall, this study reaffirms the feasibility of the use of flow devices for meaningful laser-induced oxidative labeling studies. At the same time, we provide a theoretical underpinning of this technique that goes beyond previously suggested plug flow models.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20669999     DOI: 10.1021/ac101326f

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  13 in total

1.  Validation of membrane protein topology models by oxidative labeling and mass spectrometry.

Authors:  Yan Pan; Xiang Ruan; Miguel A Valvano; Lars Konermann
Journal:  J Am Soc Mass Spectrom       Date:  2012-03-13       Impact factor: 3.109

2.  Compensated Hydroxyl Radical Protein Footprinting Measures Buffer and Excipient Effects on Conformation and Aggregation in an Adalimumab Biosimilar.

Authors:  Sandeep K Misra; Ron Orlando; Scot R Weinberger; Joshua S Sharp
Journal:  AAPS J       Date:  2019-07-11       Impact factor: 4.009

3.  High structural resolution hydroxyl radical protein footprinting reveals an extended Robo1-heparin binding interface.

Authors:  Zixuan Li; Heather Moniz; Shuo Wang; Annapoorani Ramiah; Fuming Zhang; Kelley W Moremen; Robert J Linhardt; Joshua S Sharp
Journal:  J Biol Chem       Date:  2015-03-09       Impact factor: 5.157

4.  Rapid Quantification of Peptide Oxidation Isomers From Complex Mixtures.

Authors:  Niloofar Abolhasani Khaje; Joshua S Sharp
Journal:  Anal Chem       Date:  2020-02-17       Impact factor: 6.986

Review 5.  Implementing fast photochemical oxidation of proteins (FPOP) as a footprinting approach to solve diverse problems in structural biology.

Authors:  Bojie Zhang; Ming Cheng; Don Rempel; Michael L Gross
Journal:  Methods       Date:  2018-05-23       Impact factor: 3.608

6.  Exposure of Solvent-Inaccessible Regions in the Amyloidogenic Protein Human SOD1 Determined by Hydroxyl Radical Footprinting.

Authors:  Yuewei Sheng; Joseph Capri; Alan Waring; Joan Selverstone Valentine; Julian Whitelegge
Journal:  J Am Soc Mass Spectrom       Date:  2018-10-16       Impact factor: 3.109

7.  Site-directed mutagenesis combined with oxidative methionine labeling for probing structural transitions of a membrane protein by mass spectrometry.

Authors:  Yan Pan; Leonid Brown; Lars Konermann
Journal:  J Am Soc Mass Spectrom       Date:  2010-08-13       Impact factor: 3.109

8.  Probing the Time Scale of FPOP (Fast Photochemical Oxidation of Proteins): Radical Reactions Extend Over Tens of Milliseconds.

Authors:  Siavash Vahidi; Lars Konermann
Journal:  J Am Soc Mass Spectrom       Date:  2016-04-11       Impact factor: 3.109

9.  Instant Integrated Ultradeep Quantitative-structural Membrane Proteomics Discovered Post-translational Modification Signatures for Human Cys-loop Receptor Subunit Bias.

Authors:  Xi Zhang
Journal:  Mol Cell Proteomics       Date:  2016-04-12       Impact factor: 5.911

10.  Dynamic interchanging native states of lymphotactin examined by SNAPP-MS.

Authors:  Qingyu Sun; Robert C Tyler; Brian F Volkman; Ryan R Julian
Journal:  J Am Soc Mass Spectrom       Date:  2011-01-15       Impact factor: 3.109

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.