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Peptide-based Identification of Functional Motifs and their Binding Partners
Published on: June 30, 2013
Massive peptide sharing between viral and human proteomes
Darja Kanduc1, Angela Stufano, Guglielmo Lucchese
1Department of Biochemistry and Molecular Biology, University of Bari, Bari 70126, Italy. d.kanduc@biologia.uniba.it
Abstract:
Thirty viral proteomes were examined for amino acid sequence similarity to the human proteome, and, in parallel, a control of 30 sets of human proteins was analyzed for internal human overlapping. We find that all of the analyzed 30 viral proteomes, independently of their structural or pathogenic characteristics, present a high number of pentapeptide overlaps to the human proteome. Among the examined viruses, human T-lymphotropic virus 1, Rubella virus, and hepatitis C virus present the highest number of viral overlaps to the human proteome. The widespread and ample distribution of viral amino acid sequences through the human proteome indicates that viral and human proteins are formed of common peptide backbone units and suggests a fluid compositional chimerism in phylogenetic entities canonically classified distantly as viruses and Homo sapiens. Importantly, the massive viral to human peptide overlapping calls into question the possibility of a direct causal association between virus-host sharing of amino acid sequences and incitement to autoimmune reactions through molecular recognition of common motifs.
Insights
This study reveals extensive amino acid sequence overlaps between viral and human proteomes, suggesting shared peptide building blocks. This finding challenges the distinct classification of viruses and humans and impacts understanding of autoimmune disease origins.
Area of Science:
- Virology
- Proteomics
- Immunology
- Bioinformatics
Background:
- The evolutionary relationship between viral and human proteomes is not fully understood.
- Previous research has not extensively quantified sequence similarities across diverse viral families and the human proteome.
- The role of molecular mimicry in virus-induced autoimmunity remains a key area of investigation.
Purpose of the Study:
- To systematically compare viral proteomes with the human proteome for amino acid sequence similarity.
- To investigate the extent of shared peptide motifs between viruses and humans.
- To explore the implications of these findings for viral classification and autoimmune disease pathogenesis.
Main Methods:
- Analysis of 30 viral proteomes for pentapeptide overlaps with the human proteome.
- Parallel analysis of 30 sets of human proteins for internal overlapping as a control.
- Comparative sequence analysis using bioinformatics tools to identify shared amino acid motifs.
Main Results:
- All 30 examined viral proteomes exhibited a significant number of pentapeptide overlaps with the human proteome.
- Human T-lymphotropic virus 1, Rubella virus, and hepatitis C virus showed the highest overlap frequencies.
- Widespread distribution of viral sequences within the human proteome suggests common peptide backbone units.
Conclusions:
- Viral and human proteins share common peptide building blocks, indicating compositional chimerism.
- The extensive sequence overlap challenges the strict phylogenetic separation of viruses and Homo sapiens.
- The findings raise questions about the direct causal link between viral-host sequence sharing and autoimmune reactions.
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