Literature DB >> 34057447

Platform Incubator with Movable XY Stage: A New Platform for Implementing In-Cell Fast Photochemical Oxidation of Proteins.

Danté Johnson1, Benjamin Punshon-Smith2, Jessica A Espino1, Anne Gershenson3, Lisa M Jones4.   

Abstract

Fast Photochemical Oxidation of proteins (FPOP) coupled with mass spectrometry (MS) has become an invaluable tool in structural proteomics to interrogate protein interactions, structure, and protein conformational dynamics as a function of solvent accessibility. In recent years, the scope of FPOP, a hydroxyl radical protein foot printing (HRPF) technique, has been expanded to protein labeling in live cell cultures, providing the means to study protein interactions in the convoluted cellular environment. In-cell protein modifications can provide insight into ligand induced structural changes or conformational changes accompanying protein complex formation, all within the cellular context. Protein footprinting has been accomplished employing a customary flow-based system and a 248 nm KrF excimer laser to yield hydroxyl radicals via photolysis of hydrogen peroxide, requiring 20 minutes of analysis for one cell sample.To facilitate time-resolved FPOP experiments, the use of a new 6-well plate-based IC-FPOP platform was pioneered. In the current system, a single laser pulse irradiates one entire well, which truncates the FPOP experimental time frame resulting in 20 seconds of analysis time, a 60-fold decrease. This greatly reduced analysis time makes it possible to research cellular mechanisms such as biochemical signaling cascades, protein folding, and differential experiments (i.e., drug-free vs. drug bound) in a time-dependent manner. This new instrumentation, entitled Platform Incubator with Movable XY Stage (PIXY), allows the user to perform cell culture and IC-FPOP directly on the optical bench using a platform incubator with temperature, CO2 and humidity control. The platform also includes a positioning stage, peristaltic pumps, and mirror optics for laser beam guidance. IC-FPOP conditions such as optics configuration, flow rates, transient transfections, and H2O2 concentration in PIXY have been optimized and peer-reviewed. Automation of all components of the system will reduce human manipulation and increase throughput.

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Year:  2021        PMID: 34057447      PMCID: PMC9196142          DOI: 10.3791/62153

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.424


  18 in total

1.  Fast photochemical oxidation of protein footprints faster than protein unfolding.

Authors:  Brian C Gau; Joshua S Sharp; Don L Rempel; Michael L Gross
Journal:  Anal Chem       Date:  2009-08-15       Impact factor: 6.986

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

Authors:  David M Hambly; Michael L Gross
Journal:  J Am Soc Mass Spectrom       Date:  2005-11-02       Impact factor: 3.109

Review 3.  Hydroxyl radical-mediated modification of proteins as probes for structural proteomics.

Authors:  Guozhong Xu; Mark R Chance
Journal:  Chem Rev       Date:  2007-08       Impact factor: 60.622

4.  Fast photochemical oxidation of proteins (FPOP) maps the epitope of EGFR binding to adnectin.

Authors:  Yuetian Yan; Guodong Chen; Hui Wei; Richard Y-C Huang; Jingjie Mo; Don L Rempel; Adrienne A Tymiak; Michael L Gross
Journal:  J Am Soc Mass Spectrom       Date:  2014-09-30       Impact factor: 3.109

Review 5.  Fast photochemical oxidation of proteins (FPOP): A powerful mass spectrometry-based structural proteomics tool.

Authors:  Danté T Johnson; Luciano H Di Stefano; Lisa M Jones
Journal:  J Biol Chem       Date:  2019-07-01       Impact factor: 5.157

6.  Development of a Microflow System for In-Cell Footprinting Coupled with Mass Spectrometry.

Authors:  Aimee Rinas; Vishaal S Mali; Jessica A Espino; Lisa M Jones
Journal:  Anal Chem       Date:  2016-10-07       Impact factor: 6.986

7.  Modifications generated by fast photochemical oxidation of proteins reflect the native conformations of proteins.

Authors:  Emily E Chea; Lisa M Jones
Journal:  Protein Sci       Date:  2018-04-14       Impact factor: 6.725

Review 8.  Mass Spectrometry-Based Protein Footprinting for Higher-Order Structure Analysis: Fundamentals and Applications.

Authors:  Xiaoran Roger Liu; Mengru Mira Zhang; Michael L Gross
Journal:  Chem Rev       Date:  2020-04-22       Impact factor: 60.622

Review 9.  Mass Spectrometry-Based Fast Photochemical Oxidation of Proteins (FPOP) for Higher Order Structure Characterization.

Authors:  Ke Sherry Li; Liuqing Shi; Michael L Gross
Journal:  Acc Chem Res       Date:  2018-02-16       Impact factor: 22.384

10.  Illuminating Biological Interactions with in Vivo Protein Footprinting.

Authors:  Jessica A Espino; Lisa M Jones
Journal:  Anal Chem       Date:  2019-05-07       Impact factor: 6.986

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