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  HLA-F*01:01 presents peptides with N-terminal flexibility and a preferred length of 16 residues.

Ho, G. G. T., Heinen, F. J., Huyton, T., Blasczy, R., & Bade-Döding, C. (2019). HLA-F*01:01 presents peptides with N-terminal flexibility and a preferred length of 16 residues. Immunogenetics, 51(5-6), 353-360. doi:10.1007/s00251-019-01112-1.

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 Creators:
Ho, G. G. T., Author
Heinen, F. J., Author
Huyton, Trevor1, Author           
Blasczy, R., Author
Bade-Döding, C., Author
Affiliations:
1Department of Cellular Logistics, MPI for Biophysical Chemistry, Max Planck Society, ou_578574              

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Free keywords: HLA-F; Peptides; pHLA-F model; Proteom
 Abstract: HLA-F belongs to the non-classical HLA-Ib molecules with a marginal polymorphic nature and tissue-restricted distribution. HLA-F is a ligand of the NK cell receptor KIR3DS1, whose activation initiates an antiviral downstream immune response and lead to delayed disease progression of HIV-1. During the time course of HIV infection, the expression of HLA-F is upregulated while its interaction with KIR3DS1 is diminished. Understanding HLA-F peptide selection and presentation is essential to a comprehensive understanding of this dynamic immune response and the molecules function. In this study, we were able to recover stable pHLA-F*01:01 complexes and analyze the characteristics of peptides naturally presented by HLA-F. These HLA-F-restricted peptides exhibit a non-canonical length without a defined N-terminal anchor. The peptide characteristics lead to a unique presentation profile and influence the stability of the protein. Furthermore, we demonstrate that almost all source proteins of HLA-F-restricted peptides are described to interact with HIV proteins. Understanding the balance switch between HLA-Ia and HLA-F expression and peptide selection will support to understand the role of HLA-F in viral pathogenesis.

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Language(s): eng - English
 Dates: 2019-04-242019-05
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1007/s00251-019-01112-1
 Degree: -

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Title: Immunogenetics
Source Genre: Journal
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Pages: - Volume / Issue: 51 (5-6) Sequence Number: - Start / End Page: 353 - 360 Identifier: -