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A Streamlined Approach for Mass Spectrometry-Based Proteomics Using Selected Tissue Regions
Published on: April 18, 2025
Mass spectrometry-based investigation of measles and mumps virus proteome
Dora Sviben1,2, Dubravko Forcic3,4, Beata Halassy3,4
1Centre for Research and Knowledge Transfer in Biotechnology, University of Zagreb, Rockefellerova 10, HR-10 000, Zagreb, Croatia. dora.sviben@gmail.com.
Background:
Measles (MEV) and mumps virus (MUV) are enveloped, non-segmented, negative single stranded RNA viruses of the family Paramyxoviridae, and are the cause of measles and mumps, respectively, both preventable by vaccination. Aside from proteins coded by the viral genome, viruses are considered to contain host cell proteins (HCPs). The presence of extracellular vesicles (ECVs), which are often co-purified with viruses due to their similarity in size, density and composition, also contributes to HCPs detected in virus preparations, and this has often been neglected. The aim was to identify which virus-coded proteins are present in MEV and MUV virions, and to try to detect which HCPs, if any, are incorporated inside the virions or adsorbed on their outer surface, and which are more likely to be a contamination from co-purified ECVs.
Methods:
MUV, MEV and ECVs were purified by ultracentrifugation, hydrophobic interaction chromatography and immunoaffinity chromatography, proteins in the samples were resolved by SDS-PAGE and subjected to identification by MALDI-TOF/TOF-MS. A comparative analysis of HCPs present in all samples was carried out.
Results:
By proteomics approach, it was verified that almost all virus-coded proteins are present in MEV and MUV particles. Protein C in MEV which was until now considered to be non-structural viral protein, was found to be present inside the MeV virions. Results on the presence of HCPs in differently purified virus preparations imply that actin, annexins, cyclophilin A, moesin and integrin β1 are part of the virions.
Conclusions:
All HCPs detected in the viruses are present in ECVs as well, indicating their possible function in vesicle formation, or that most of them are only present in ECVs. Only five HCPs were constantly present in purified virus preparations, regardless of the purification method used, implying they are likely the integral part of the virions. The approach described here is helpful for further investigation of HCPs in other virus preparations.
Insights
This study identified viral and host cell proteins in measles (MEV) and mumps (MUV) virus preparations. Five host cell proteins were consistently found, suggesting they are integral to the virions, not just contaminants.
Area of Science:
- Virology
- Proteomics
- Cell Biology
Background:
- Measles virus (MEV) and mumps virus (MUV) are Paramyxoviridae family viruses responsible for measles and mumps.
- Viral preparations can contain host cell proteins (HCPs) and extracellular vesicles (ECVs), complicating analysis.
- Distinguishing virion-associated proteins from contaminants is crucial for understanding viral structure and function.
Purpose of the Study:
- To identify virus-coded proteins within MEV and MUV virions.
- To detect and differentiate HCPs associated with virions versus those from co-purified ECVs.
- To clarify the composition of purified paramyxovirus preparations.
Main Methods:
- Purification of MUV, MEV, and ECVs using ultracentrifugation, hydrophobic interaction chromatography, and immunoaffinity chromatography.
- Protein separation via SDS-PAGE.
- Protein identification using MALDI-TOF/TOF-MS and comparative HCP analysis.
Main Results:
- Proteomics confirmed the presence of nearly all virus-coded proteins in MEV and MUV particles.
- Protein C, previously considered non-structural, was identified within MEV virions.
- Actin, annexins, cyclophilin A, moesin, and integrin β1 were identified as potential integral virion components.
Conclusions:
- All detected HCPs were also found in ECVs, suggesting a role in vesicle formation or ECV association.
- Five specific HCPs were consistently present across different purification methods, indicating they are likely integral to the virions.
- The described proteomics approach aids in the investigation of HCPs in other viral systems.
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Mass Spectrometry of Amines
Chemical Ionization (CI) Mass Spectrometry
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