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Article abstracts
Main reference:
NetMHCpan - MHC class I binding prediction beyond humans
Hoof I1,
Peter B3,
Sidney J3,
Pedersen LE2
Lund O1,
Buus S2,
Nielsen M1,
Immunogenetics. 2009 Jan;61(1):1-13.
1Center for Biological Sequence Analysis,
Technical University of Denmark,
DK-2800 Lyngby, Denmark
2Division of Experimental Immunology,
Institute of Medical Microbiology and Immunology,
University of Copenhagen, Denmark
3La Jolla Institute for Allergy and Immunology, San Diego, California, United States of America
Binding of peptides to major histocompatibility complex (MHC) molecules
is the single most selective step in the recognition of pathogens by
the cellular immune system. The human MHC genomic region (called HLA)
is extremely polymorphic comprising several thousand alleles, each
encoding a distinct MHC molecule. The potentially unique specificity
of the majority of HLA alleles that have been identified to date
remains uncharacterized. Likewise, only a limited number of chimpanzee
and rhesus macaque MHC class I molecules have been characterized
experimentally. Here, we present NetMHCpan-2.0, a method that generates
quantitative predictions of the affinity of any peptide-MHC class I
interaction. NetMHCpan-2.0 has been trained on the hitherto largest set
of quantitative MHC binding data available, covering HLA-A and HLA-B,
as well as chimpanzee, rhesus macaque, gorilla, and mouse MHC class
I molecules. We show that the NetMHCpan-2.0 method can accurately
predict binding to uncharacterized HLA molecules, including HLA-C and
HLA-G. Moreover, NetMHCpan-2.0 is demonstrated to accurately predict
peptide binding to chimpanzee and macaque MHC class I molecules. The power
of NetMHCpan-2.0 to guide immunologists in interpreting cellular immune
responses in large out-bred populations is demonstrated. Further, we used
NetMHCpan-2.0 to predict potential binding peptides for the pig MHC class
I molecule SLA-1*0401. Ninety-three percent of the predicted peptides
were demonstrated to bind stronger than 500 nM. The high performance
of NetMHCpan-2.0 for non-human primates documents the method's ability
to provide broad allelic coverage also beyond human MHC molecules. The
method is available at http://www.cbs.dtu.dk/services/NetMHCpan.
PMID: 19002680
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CORRESPONDENCE
Morten Nielsen,
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