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Biophysical analysis of BMV virions purified using a novel method

•We present a novel purification procedure for BMV.•We confirm high stability of the BMV capsid in pH range from 5.6 to 8.4.•We present results of secondary structure analysis of BMV capsid protein. Brome mosaic virus (BMV) has been successfully loaded with different types of nanoparticles. However,...

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Published in:Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2017-11, Vol.1068-1069, p.157-163
Main Authors: Strugała, Aleksander, Kręcisz, Monika, Rybka, Jakub Dalibor, Urbanowicz, Anna, Szpotkowski, Kamil, Bierwagen, Paulina, Figlerowicz, Marek, Kozak, Maciej, Böttcher, Christoph, Giersig, Michał
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cited_by cdi_FETCH-LOGICAL-c365t-6fc9a30488a6b3532f1239a137e1447d129525a81c124702c112e92eb2e564023
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container_title Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
container_volume 1068-1069
creator Strugała, Aleksander
Kręcisz, Monika
Rybka, Jakub Dalibor
Urbanowicz, Anna
Szpotkowski, Kamil
Bierwagen, Paulina
Figlerowicz, Marek
Kozak, Maciej
Böttcher, Christoph
Giersig, Michał
description •We present a novel purification procedure for BMV.•We confirm high stability of the BMV capsid in pH range from 5.6 to 8.4.•We present results of secondary structure analysis of BMV capsid protein. Brome mosaic virus (BMV) has been successfully loaded with different types of nanoparticles. However, studies concerning its application as a nanoparticle carrier demand high-purity virions in large amounts. Existing BMV purification protocols rely on multiple differential ultracentrifugation runs of the initially purified viral preparation. Herein, we describe an alternative method for BMV purification based on ion-exchange chromatography and size-exclusion chromatography (SEC) yielding 0.2mg of virus from 1g of plant tissue. Our method is of similar efficiency to previously described protocols and can easily be scaled up. The method results in high-quality BMV preparations as confirmed by biophysical analyses, including cryogenic transmission electron microscopy (cryo-TEM), dynamic light scattering (DLS), static light scattering (SLS), and circular dichroism (CD) measurements and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) spectroscopy. Our results revealed that purified BMV capsids are stable and monodisperse and can be used for further downstream applications. In this work, we also characterize secondary structure and size fluctuations of the BMV virion at different pH values.
doi_str_mv 10.1016/j.jchromb.2017.10.022
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Brome mosaic virus (BMV) has been successfully loaded with different types of nanoparticles. However, studies concerning its application as a nanoparticle carrier demand high-purity virions in large amounts. Existing BMV purification protocols rely on multiple differential ultracentrifugation runs of the initially purified viral preparation. Herein, we describe an alternative method for BMV purification based on ion-exchange chromatography and size-exclusion chromatography (SEC) yielding 0.2mg of virus from 1g of plant tissue. Our method is of similar efficiency to previously described protocols and can easily be scaled up. The method results in high-quality BMV preparations as confirmed by biophysical analyses, including cryogenic transmission electron microscopy (cryo-TEM), dynamic light scattering (DLS), static light scattering (SLS), and circular dichroism (CD) measurements and attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) spectroscopy. Our results revealed that purified BMV capsids are stable and monodisperse and can be used for further downstream applications. 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B, Analytical technologies in the biomedical and life sciences</title><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><description>•We present a novel purification procedure for BMV.•We confirm high stability of the BMV capsid in pH range from 5.6 to 8.4.•We present results of secondary structure analysis of BMV capsid protein. Brome mosaic virus (BMV) has been successfully loaded with different types of nanoparticles. However, studies concerning its application as a nanoparticle carrier demand high-purity virions in large amounts. Existing BMV purification protocols rely on multiple differential ultracentrifugation runs of the initially purified viral preparation. Herein, we describe an alternative method for BMV purification based on ion-exchange chromatography and size-exclusion chromatography (SEC) yielding 0.2mg of virus from 1g of plant tissue. Our method is of similar efficiency to previously described protocols and can easily be scaled up. 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subjects Brome mosaic virus
Bromovirus - chemistry
Bromovirus - isolation & purification
Chromatography, Gel
Chromatography, Ion Exchange - methods
Circular Dichroism
Cryogenic transmission electron microscopy
Fourier transform infrared spectroscopy
Hordeum - metabolism
Hordeum - virology
Light
Light scattering
Microscopy, Electron, Transmission
Scattering, Radiation
Spectroscopy, Fourier Transform Infrared
Virion - chemistry
Virion - isolation & purification
title Biophysical analysis of BMV virions purified using a novel method
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