Method Article

Time-resolved ElectroSpray Ionization Hydrogen-deuterium Exchange Mass Spectrometry for Studying Protein Structure and Dynamics

DOI:

10.3791/55464

April 17th, 2017

In This Article

Summary

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Conformational flexibility plays a critical role in protein function. Herein, we describe the use of time-resolved electrospray ionization mass spectrometry coupled to hydrogen-deuterium exchange for probing the rapid structural changes that drive function in ordered and disordered proteins.

Abstract

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Intrinsically disordered proteins (IDPs) have long been a challenge to structural biologists due to their lack of stable secondary structure elements. Hydrogen-Deuterium Exchange (HDX) measured at rapid time scales is uniquely suited to detect structures and hydrogen bonding networks that are briefly populated, allowing for the characterization of transient conformers in native ensembles. Coupling of HDX to mass spectrometry offers several key advantages, including high sensitivity, low sample consumption and no restriction on protein size. This technique has advanced greatly in the last several decades, including the ability to monitor HDX labeling times on the millisecond time scale. In addition, by incorporating the HDX workflow onto a microfluidic platform housing an acidic protease microreactor, we are able to localize dynamic properties at the peptide level. In this study, Time-Resolved ElectroSpray Ionization Mass Spectrometry (TRESI-MS) coupled to HDX was used to provide a detailed picture of residual structure in the tau protein, as well as the conformational shifts induced upon hyperphosphorylation.

Introduction

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Over the past several decades, significant advancements have been made in the development of analytical techniques designed to measure protein structure and dynamics1,2,3,4. While X-ray crystallography remains the principle tool for determining protein structure, high concentrations of protein are needed and extensive optimization is required to produce diffraction quality crystals. Proteins that are difficult to crystallize, such as membrane-associated and intrinsically disordered proteins have classically been studied by hydrogen-deuterium....

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Protocol

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NOTE: Please consult all relevant material safety data sheets (MSDS) before use. Fumes produced by laser ablation of poly(methyl methacrylate) (PMMA) can be toxic. Be sure that the laser engraver is connected to a working ventilation system. Use all appropriate safety practices when building the microfluidic device including the use of engineering controls (fume hood, sharps container) and personal protective equipment (safety glasses, face mask, gloves, lab coat, full length pants, closed-toe shoes). It is of utmost importance to use High Performance Liquid Chromatography (HPLC) grade reagents whenever possible, with all being of ACS grade or higher to decrease inter....

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Results

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Digestion profiles of native and phospho-tau were similar, yielding a sequence coverage of 77.1 and 71.7% respectively. Deuterium uptake values of each peptide was determined by fitting the observed isotopic distributions with the theoretical distributions generated using an in-house developed FORTRAN software. The best fitting distributions are shown (Figure 3a) along with the associated deuterium uptake values. Uptake kinetic profiles are then generated, and were well d.......

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Discussion

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While structural biology methods such as X-ray crystallography and NMR are advantageous because they provide extremely detailed structures of proteins, these pictures are often static. The characterization of transient species and weakly structured domains continues to be elusive when studied by these conventional methods. Therefore, in order to gain dynamic insights on these types of systems it is important to work at rapid time scales. We have successfully applied TRESI-HDX-MS to obtain detailed insights on the conform.......

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Disclosures

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We have nothing to disclose.

Acknowledgements

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We gratefully acknowledge Dr. Markus Zweckstetter for providing the pdb coordinate file for the 'native' tau ensemble predicted from his NMR work, with contributed analysis tools provided by Dr. Adnan Sljoka. Funding for this work was provided by the Natural Science and Engineering Research Council of Canada (NSERC) ENGAGE Grant program.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Poly(methyl methacrylate) or PMMAProfessional PlasticsSACR.250CCP8.9 cm x 3.8 cm x 0.6 cm
Fused Silica Glass CapillaryPolymicro Technologies106815-0018ID: 75 µm, OD: 150 µm
Metal CapillariesMcMaster-Carr28 ga – 89875K97
30 ga  - 89875K99
Fluorinated Ethylene Propylene (FEP) TubingIDEX1477
1548
ID: 0.007”, OD: 1/16”
ID: 0.020”, OD: 1/16”
Standard Polymer Tubing CutterIDEXA-327for 1/16” and 1/8” OD tubing
Micro Static Mixing TeeIDEXM-540for 1/16” OD tubing
or
Stainless Steel Tee, 0.25 mm BoreValco Instruments Co., Inc. (VICI)ZT1Cfor 1/16” OD tubing
PEEK Tee for 1/16” OD TubingIDEXP-727
10-32 Female to Female LuerIDEXP-659
10-32 PEEK Double-Winged NutIDEXF-300
Ferrule for 1/16” OD TubingIDEXF-142
100 Series Rotary ToolDremelF013010001
Cut-Off DiscsJobmate1/64” thickness
Stereomaster Digital Zoom MicroscopeFisher Scientific12-563-411
Soldering IronMastercraft58-6301-2
VersaLaserUniversal Laser
SyringesHamilton81220500 µL capacity
Syringe PumpsHarvard Apparatus70-4501
NameCompanyCatalog NumberComments
Reagents
NHS-Activated AgaroseFisher Scientific26196
Pepsin from Porcine Gastric MucosaSigma-AldrichP6887-250MG
Deuterium OxideSigma-Aldrich151882-10X0.6ML
Acetic AcidSigma-Aldrich695092-100ML
HPLC Grade WaterFisher ScientificW5-4
Ammonium AcetateSigma-AldrichA7330-500G
Sodium PhosphateFisher ScientificS369-500
Sodium ChlorideFisher ScientificS671-3
NameCompanyCatalog NumberComments
Software/Online Tools
CorelDraw X3Corel
Molecular Weight CalculatorVersion 6.49Open Source MS Tool
mMassVersion 5.5.0Open Source MS Tool
ExPASy FindPeptSwiss Institute of Bioinformatics
SigmaPlotSystat SoftwareVersion 11.0
PyMOLSchrödingerVersion 1.5.0.4
NameCompanyCatalog NumberComments
Instruments
QStar Elite Hybrid Q-TOF Mass SpectrometerAB SCIEX

References

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  1. Sapienza, P. J., Lee, A. L. Using NMR to study fast dynamics in proteins: methods and applications. Curr. Opin. Pharmacol. 10, 723-730 (2010).
  2. Neira, J. L. NMR as a tool to identify and characterize protein folding intermediates. Arch. Biochem. B....

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Tags

Protein Structure AnalysisIntrinsically Disordered ProteinsTau Protein DynamicsPeptide Level MappingMillisecond Time ScaleMicrofluidic PlatformConformational Shifts

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