Comparison of sample preparation techniques for the physicochemical characterization of Orf virus particles

Elsevier

Available online 6 September 2022, 114614

Journal of Virological MethodsHighlights•

Evaluation of three rapid virus sample preparation methods

Virus preparation methods impact charge and size measurements

Diafiltration introduces Orf virus aggregates and reduces virus recovery

Ultracentrifugation is best suited for high virus titers

Virus charge characterization after steric exclusion chromatography possible

Abstract

The determination of the electrostatic charge of biological nanoparticles requires a purified, mono-disperse, and concentrated sample. Previous studies proofed an impact of the preparation protocol on the stability and electro-hydrodynamics of viruses, whereas commonly used methods are often complex and do not allow the required sample throughput. In the present study, the application of the (I) steric exclusion chromatography (SXC) for the Orf virus (ORFV) purification and subsequent physicochemical characterization was evaluated and compared to (II) SXC followed by centrifugal diafiltration and (III) sucrose cushion ultracentrifugation. The three methods were characterized in terms of protein removal, size distribution, infectious virus recovery, visual appearance, and electrophoretic mobility as a function of pH. All preparation techniques achieved a protein removal of more than 99%, and (I) an infectious ORFV recovery of more than 85%. Monodisperse samples were realized by (I) and (III). In summary, ORFV samples prepared by (I) and (III) displayed comparable quality. Additionally, (I) offered the shortest operation time and easy application. Based on the obtained data, the three procedures were ranked according to eight criteria of possible practical relevance, which delineate the potential of SXC as virus preparation method for physicochemical analysis.

AbbreviationsCPB

citrate phosphate buffer

DLS

dynamic light scattering

MWCO

molecular weight cut-off

PBS

phosphate buffered saline

PEG

polyethylene glycol, PEG8000 corresponds to 8000 Da

SC

sucrose density gradient centrifugation

SXC

steric exclusion chromatography

SXC-DF

steric exclusion chromatography with subsequent diafiltration

TEM

transmission electron microscopy

Keywords

isoelectric point

Orf virus

surface charge

transmission electron microscopy

viral vector vaccine

zeta potential

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