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Whole-Proteome Peptide Microarrays for Profiling Autoantibody Repertoires within Multiple Sclerosis and Narcolepsy

Zandian, Arash (author)
KTH,Proteomik och nanobioteknologi,Science for Life Laboratory, SciLifeLab
Forsström, Björn (author)
KTH,Albanova VinnExcellence Center for Protein Technology, ProNova,Proteomik och nanobioteknologi,Science for Life Laboratory, SciLifeLab
Häggmark-Månberg, Anna (author)
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Schwenk, Jochen M. (author)
KTH,Proteomik,Nanobioteknologi,Science for Life Laboratory, SciLifeLab,Proteomik och nanobioteknologi
Uhlén, Mathias (author)
KTH,Proteomik och nanobioteknologi
Nilsson, Peter (author)
KTH,Proteomik och nanobioteknologi,Science for Life Laboratory, SciLifeLab
Ayoglu, Burcu (author)
KTH,Proteomik och nanobioteknologi,Science for Life Laboratory, SciLifeLab
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 (creator_code:org_t)
2017-02-09
2017
English.
In: Journal of Proteome Research. - : American Chemical Society (ACS). - 1535-3893 .- 1535-3907. ; 16:3, s. 1300-1314
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The underlying molecular mechanisms of autoimmune diseases are poorly understood. To unravel the autoimmune processes across diseases, comprehensive and unbiased analyses of proteins targets recognized by the adaptive immune system are needed. Here we present an approach starting from high-density peptide arrays to characterize autoantibody repertoires and to identify new autoantigens. A set of ten plasma and serum samples from subjects with multiple sclerosis, narcolepsy, and without any disease diagnosis were profiled on a peptide array representing the whole proteome, hosting 2.2 million 12-mer peptides with a six amino acid lateral shift. On the basis of the IgG reactivities found on these whole-proteome peptide micro arrays, a set of 23 samples was then studied on a targeted array with 174 000 12-mer peptides of single amino acid lateral shift. Finally, verification of IgG reactivities was conducted with a larger sample set (n = 448) using the bead-based peptide microarrays. The presented workflow employed three different peptide microarray formats to discover and resolve the epitopes of human autoantibodies and revealed two potentially new autoantigens: MAP3K7 in multiple sclerosis and NRXN1 in narcolepsy. The presented strategy provides insights into antibody repertoire reactivity at a peptide level and may accelerate the discovery and validation of autoantigens in human diseases.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)

Keyword

peptide microarrays
autoantibody profiling
epitope mapping narcolepsy
multiple sclerosis

Publication and Content Type

ref (subject category)
art (subject category)

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