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Mass spectrometry-based technologies for probing the 3D world of plant proteins

Journal Article · · Plant Physiology (Bethesda)
 [1];  [1];  [1]
  1. Department of Biochemistry and Center for Genomic Science Innovation, University of Wisconsin, Madison, Wisconsin 53706, USA

Abstract Over the past two decades, mass spectrometric (MS)-based proteomics technologies have facilitated the study of signaling pathways throughout biology. Nowhere is this needed more than in plants, where an evolutionary history of genome duplications has resulted in large gene families involved in posttranslational modifications and regulatory pathways. For example, at least 5% of the Arabidopsis thaliana genome (ca. 1,200 genes) encodes protein kinases and protein phosphatases that regulate nearly all aspects of plant growth and development. MS-based technologies that quantify covalent changes in the side-chain of amino acids are critically important, but they only address one piece of the puzzle. A more crucially important mechanistic question is how noncovalent interactions—which are more difficult to study—dynamically regulate the proteome’s 3D structure. The advent of improvements in protein 3D technologies such as cryo-electron microscopy, nuclear magnetic resonance, and X-ray crystallography has allowed considerable progress to be made at this level, but these methods are typically limited to analyzing proteins, which can be expressed and purified in milligram quantities. Newly emerging MS-based technologies have recently been developed for studying the 3D structure of proteins. Importantly, these methods do not require protein samples to be purified and require smaller amounts of sample, opening the wider proteome for structural analysis in complex mixtures, crude lysates, and even in intact cells. These MS-based methods include covalent labeling, crosslinking, thermal proteome profiling, and limited proteolysis, all of which can be leveraged by established MS workflows, as well as newly emerging methods capable of analyzing intact macromolecules and the complexes they form. In this review, we discuss these recent innovations in MS-based “structural” proteomics to provide readers with an understanding of the opportunities they offer and the remaining challenges for understanding the molecular underpinnings of plant structure and function.

Research Organization:
Univ. of Wisconsin, Madison, WI (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
DOE Contract Number:
FG02-88ER13938
OSTI ID:
1979585
Journal Information:
Plant Physiology (Bethesda), Vol. 189, Issue 1; ISSN 0032-0889
Publisher:
American Society of Plant Biologists
Country of Publication:
United States
Language:
English

References (38)

How many human proteoforms are there? journal February 2018
Analysis of the genome sequence of the flowering plant Arabidopsis thaliana journal December 2000
Intact ribosomes drive the formation of protein quinary structure journal April 2020
Comparative Analysis of Mass-Spectrometry-Based Proteomic Methods for Protein Target Discovery Using a One-Pot Approach journal November 2019
Dynamic 3D proteomes reveal protein functional alterations at high resolution in situ journal January 2021
Protein Footprinting: Auxiliary Engine to Power the Structural Biology Revolution journal April 2020
Plasma Membrane H + -ATPase Regulation in the Center of Plant Physiology journal March 2016
Crowding in Cellular Environments at an Atomistic Level from Computer Simulations journal July 2017
Retrieval of DNA Using Soft-Landing after Mass Analysis by ESI-FTICR for Enzymatic Manipulation journal September 1999
Protein folding and surface interaction phase diagrams in vitro and in cells journal March 2021
Weak Chemical Interactions That Drive Protein Evolution: Crowding, Sticking, and Quinary Structure in Folding and Function journal July 2019
Regulation of the plasma membrane proton pump (H+-ATPase) by phosphorylation journal December 2015
Proteome-Wide Structural Biology: An Emerging Field for the Structural Analysis of Proteins on the Proteomic Scale journal September 2018
High-Resolution Hydroxyl Radical Protein Footprinting: Biophysics Tool for Drug Discovery journal May 2018
Protein Quantitation Using Isotope-Assisted Mass Spectrometry journal April 2010
Comparing samples—part II journal March 2014
Probing a Plant Plasma Membrane Receptor Kinase’s Three-Dimensional Structure Using Mass Spectrometry-Based Protein Footprinting journal August 2018
Mass Spectrometry-Based Protein Footprinting for Higher-Order Structure Analysis: Fundamentals and Applications journal April 2020
Chemo-Selection Strategy for Limited Proteolysis Experiments on the Proteomic Scale journal November 2018
Identification of tryptic cleavage sites for two conformational states of the Neurospora plasma membrane H+-ATPase. journal October 1988
Chemical Denaturation and Protein Precipitation Approach for Discovery and Quantitation of Protein–Drug Interactions journal July 2018
Plasma-Generated OH Radical Production for Analyzing Three-Dimensional Structure in Protein Therapeutics journal October 2017
Slow-Down in Diffusion in Crowded Protein Solutions Correlates with Transient Cluster Formation journal November 2017
Intermolecular and Intramolecular Interactions of the Arabidopsis Plasma Membrane Proton Pump Revealed Using a Mass Spectrometry Cleavable Cross-Linker journal May 2020
In vivo cross-linking supports a head-to-tail mechanism for regulation of the plant plasma membrane P-type H+-ATPase journal November 2018
A general method for site-specific incorporation of unnatural amino acids into proteins journal April 1989
Preparing Protein Microarrays by Soft-Landing of Mass-Selected Ions journal September 2003
Crystal structure of the plasma membrane proton pump journal December 2007
Mass Spectrometry-Based De Novo Sequencing of Monoclonal Antibodies Using Multiple Proteases and a Dual Fragmentation Scheme journal June 2021
Detecting Protein–Small Molecule Interactions Using Limited Proteolysis–Mass Spectrometry (LiP-MS) journal October 2020
In-Cell Protein–Protein Contacts: Transient Interactions in the Crowd journal September 2019
Tracking cancer drugs in living cells by thermal profiling of the proteome journal October 2014
Proteoforms as the next proteomics currency journal March 2018
Characterization of Residue Specific Protein Folding and Unfolding Dynamics in Cells journal July 2019
High-fidelity mass analysis unveils heterogeneity in intact ribosomal particles journal January 2017
Proteome-wide Analysis of Protein Thermal Stability in the Model Higher Plant Arabidopsis thaliana journal February 2019
Protein Folding Stability Changes Across the Proteome Reveal Targets of Cu Toxicity in E. coli journal December 2020
Advances in integrative structural biology: Towards understanding protein complexes in their cellular context journal January 2021