Single amino acid fingerprinting of the human antibody repertoire with high density peptide arrays
The antibody species that patrol in a patient's blood are an invaluable part of the immune system. While most of them shield us from life-threatening infections, some of them do harm in autoimmune diseases. If we knew exactly all the antigens that elicited all the antibody species within a grou...
Gespeichert in:
| Hauptverfasser: | , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
3 February 2017
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| In: |
Journal of immunological methods
Year: 2017, Jahrgang: 443, Pages: 45-54 |
| ISSN: | 1872-7905 |
| DOI: | 10.1016/j.jim.2017.01.012 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1016/j.jim.2017.01.012 Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S0022175916302903 
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| Verfasserangaben: | Laura K. Weber, Andrea Palermo, Jonas Kügler, Olivier Armant, Awale Isse, Simone Rentschler, Thomas Jaenisch, Jürgen Hubbuch, Stefan Dübel, Alexander Nesterov-Mueller, Frank Breitling, Felix F. Loeffler |
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| 245 | 1 | 0 | |a Single amino acid fingerprinting of the human antibody repertoire with high density peptide arrays |c Laura K. Weber, Andrea Palermo, Jonas Kügler, Olivier Armant, Awale Isse, Simone Rentschler, Thomas Jaenisch, Jürgen Hubbuch, Stefan Dübel, Alexander Nesterov-Mueller, Frank Breitling, Felix F. Loeffler |
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| 520 | |a The antibody species that patrol in a patient's blood are an invaluable part of the immune system. While most of them shield us from life-threatening infections, some of them do harm in autoimmune diseases. If we knew exactly all the antigens that elicited all the antibody species within a group of patients, we could learn which ones correlate with immune protection, are irrelevant, or do harm. Here, we demonstrate an approach to this question: First, we use a plethora of phage-displayed peptides to identify many different serum antibody binding peptides. Next, we synthesize identified peptides in the array format and rescreen the serum used for phage panning to validate antibody binding peptides. Finally, we systematically vary the sequence of validated antibody binding peptides to identify those amino acids within the peptides that are crucial for binding “their” antibody species. The resulting immune fingerprints can then be used to trace them back to potential antigens. We investigated the serum of an individual in this pipeline, which led to the identification of 73 antibody fingerprints. Some fingerprints could be traced back to their most likely antigen, for example the immunodominant capsid protein VP1 of enteroviruses, most likely elicited by the ubiquitous poliovirus vaccination. Thus, with our approach, it is possible, to pinpoint those antibody species that correlate with a certain antigen, without any pre-information. This can help to unravel hitherto enigmatic diseases. | ||
| 650 | 4 | |a Humoral immune system | |
| 650 | 4 | |a Next generation sequencing | |
| 650 | 4 | |a Phage display | |
| 650 | 4 | |a Serology | |
| 650 | 4 | |a Substitution analysis | |
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