Method Article

A Tailored HPLC Purification Protocol That Yields High-purity Amyloid Beta 42 and Amyloid Beta 40 Peptides, Capable of Oligomer Formation

DOI:

10.3791/55482

March 27th, 2017

In This Article

Summary

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Herein we report a tailored HPLC purification protocol that yields high-purity amyloid beta 42 (Aβ42) and amyloid beta 40 (Aβ40) peptides, capable of oligomer formation. Amyloid beta is a highly aggregation prone, hydrophobic peptide implicated in Alzheimer's disease. The amyloidogenic nature of the peptide makes its purification a challenge.

Abstract

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Amyloidogenic peptides such as the Alzheimer's disease-implicated Amyloid beta (Aβ), can present a significant challenge when trying to obtain high purity material. Here we present a tailored HPLC purification protocol to produce high-purity amyloid beta 42 (Aβ42) and amyloid beta 40 (Aβ40) peptides. We have found that the combination of commercially available hydrophobic poly(styrene/divinylbenzene) stationary phase, polymer laboratory reverse phase - styrenedivinylbenzene (PLRP-S) under high pH conditions, enables the attainment of high purity (>95%) Aβ42 in a single chromatographic run. The purification is highly reproducible and can be amended to both semi-preparative and analytical conditions depending upon the amount of material wished to be purified. The protocol can also be applied to the Aβ40 peptide with identical success and without the need to alter the method.

Introduction

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Alzheimer's disease is a neurodegenerative disorder that effects over 35 million people worldwide.1 Implicated strongly in the onset and development of the disease, is the highly aggregation prone, hydrophobic peptide Amyloid beta (Aβ).2 Aβ ranges from 36 to 43 amino acids in length, however, it is thought that the 42-amino acid variant, amyloid beta 42 (Aβ42), is the most toxic form of the protein.3 This is due in most part to the ability of Aβ42 to readily form diffusible, oligomeric species that are believed to be particularly neurotoxic entities.4

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Protocol

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1. Preparative HPLC Purification of the Aβ40 or Aβ42 Peptide

  1. Prepare the following buffers for the HPLC purification.
    1. Prepare buffer A (20 mM NH4OH) by adding 1.3 mL of NH4OH (28% solution) to 1,000 mL of ultrapure water.
    2. Prepare buffer B (80% acetonitrile with 20 mM NH4OH) by adding 1.3 mL of NH4OH (28% solution) to a solution of 800 mL of HPLC-grade acetonitrile and 200 mL of ultrapure water.
    3. Prepare sample dissolution buffer (0.1% NH4OH) by adding 100 µL of NH4OH (28% solution) to 100 mL of ultrapure water.

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Results

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The purification of the Aβ42 peptide using a combination of the PLRP-S stationary phase and a high pH mobile phase results in the formation of a sharp, resolved peak for the Aβ peptide at a retention time between 72 and 74 min (Figure 2C). Confirmation of the identity of the peak is done through direct injection mass spectrometry of the collected eluent. The eluent can be stored at -20 °C in solution for up to 12 h. Longer periods of storage may result in oxidation of the.......

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Discussion

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The HPLC purification of the Aβ peptide is highly dependent upon the choice of both the stationary phase employed in the purification and the mobile phase chosen to elute the peptide. The low isoelectric point of the peptide and high propensity for aggregation render traditional chromatographic conditions for the separation of hydrophobic proteins (C4 or C8 stationary phase coupled with an acidic mobile eluent) challenging, with the Aβ peptide eluting as a prolonged broad, non-resolved peak (Figure 2A

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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The authors would like to thank Agilent for their technical assistance. Kate Markham and Rafael Palomino are credited for their initial help in the synthesis and purification of the Aβ peptide and Dr Hsiau-Wei Lee is thanked for his help in preparing Figure 1 of the manuscript.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Agilent 1260 Infinity II quarternary pumpAgilentG7111Bhttp://www.agilent.com/en-us/products/liquid-chromatography/lc-pumps-vacuum-degassers/1260-infinity-ii-quaternary-pump
Agilent 1260 Infinity II Dual variable wavelength detectorAgilentG7114Ahttp://www.agilent.com/en-us/products/liquid-chromatography/lc-detectors/1260-infinity-ii-variable-wavelength-detector
Agilent 1260 Infinity II Manual Injector fitted with 10 mL stainless steel sample loopAgilent0101-1232http://www.agilent.com/en-us/products/liquid-chromatography/lc-injection-systems/1260-infinity-ii-manual-injector
Agilent 1260 Infinity II Manual Injector fitted with 20 µL stainless steel sample loopAgilentG1328Chttp://www.agilent.com/en-us/products/liquid-chromatography/lc-injection-systems/1260-infinity-ii-manual-injector
Ring Stand Mounting BracketAgilent1400-3166
Agilent PLRP-S 300 Å 5 µm 4.6 x 250 mm (Analytical)AgilentPL1512-5501http://www.agilent.com/en-us/products/liquid-chromatography/lc-columns/biomolecule-separations/plrp-s-for-biomolecules#features
Aβ42 or Aβ40 peptideSynthesized in-house using a CEM liberty automated peptide synthesizer.
Ammonium Hydroxide (NH4OH, 28% solution)Fisher ScientificA669-500
AcetonitrileFisher ScientificA998-4
HPLC grade waterFisher ScientificW5-4
Falcon 50 mL conical centrifuge tubeFisher Scientific14-954-49A
Supelco PEEK Fitting One-piece fingertight, pkg of 5 eaSigma-AldrichZ227250
Normject 5 cc sterile syringeFisher Scientific1481729
16 Gauge SS NeedleRheodyne3725-086

References

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  1. Querfurth, H. W., LaFerla, F. M. Alzheimer's Disease. N. Engl. J. Med. 362 (4), 329-344 (2010).
  2. McGowan, E., et al. Aβ42 Is Essential for Parenchymal and Vascular Amyloid Deposition in Mice. Neuron. 47 (2), 191-199 (2005).
  3. Gong, Y., et al. Alzheimer's disease....

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Tags

HPLC PurificationAmyloid Beta 42Amyloid Beta 40Peptide Oligomer FormationPolymer Stationary PhaseHigh pH ConditionsPreparative ColumnDual Wavelength DetectorBuffer EquilibrationSample Dissolution

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