Conformational epitopes on the diabetes autoantigen GAD65 identified by peptide phage display and molecular modeling

Myers, Mark A., Davies, Janet M., Tong, Jonathan C., Whisstock, James, Scealy, Marita, Mackay, Ian R. and Rowley, Merrill J. (2000) Conformational epitopes on the diabetes autoantigen GAD65 identified by peptide phage display and molecular modeling. Journal of Immunology, 165 7: 3830-3838.

Author Myers, Mark A.
Davies, Janet M.
Tong, Jonathan C.
Whisstock, James
Scealy, Marita
Mackay, Ian R.
Rowley, Merrill J.
Title Conformational epitopes on the diabetes autoantigen GAD65 identified by peptide phage display and molecular modeling
Journal name Journal of Immunology   Check publisher's open access policy
ISSN 0022-1767
1550-6606
Publication date 2000-10-01
Sub-type Article (original research)
Volume 165
Issue 7
Start page 3830
End page 3838
Total pages 9
Place of publication Bethesda, MD, United States
Publisher American Association of Immunologists
Language eng
Formatted abstract
The major diabetes autoantigen, glutamic acid decarboxylase (GAD65), contains a region of sequence similarity, including six identical residues PEVKEK, to the P2C protein of coxsackie B virus, suggesting that cross-reactivity between coxsackie B virus and GAD65 can initiate autoimmune diabetes. We used the human islet cell mAbs MICA3 and MICA4 to identify the Ab epitopes of GAD65 by screening phage-displayed random peptide libraries. The identified peptide sequences could be mapped to a homology model of the pyridoxal phosphate (PLP) binding domain of GAD65. For MICA3, a surface loop containing the sequence PEVKEK and two adjacent exposed helixes were identified in the PLP binding domain as well as a region of the C terminus of GAD65 that has previously been identified as critical for MICA3 binding. To confirm that the loop containing the PEVKEK sequence contributes to the MICA3 epitope, this loop was deleted by mutagenesis. This reduced binding of MICA3 by 70%. Peptide sequences selected using MICA4 were rich in basic or hydroxyl-containing amino acids, and the surface of the GAD65 PLP-binding domain surrounding Lys358, which is known to be critical for MICA4 binding, was likewise rich in these amino acids. Also, the two phage most reactive with MICA4 encoded the motif VALxG, and the reverse of this sequence, LAV, was located in this same region. Thus, we have defined the MICA3 and MICA4 epitopes on GAD65 using the combination of phage display, molecular modeling, and mutagenesis and have provided compelling evidence for the involvement of the PEVKEK loop in the MICA3 epitope.
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collection: School of Medicine Publications
 
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Created: Tue, 17 Nov 2009, 22:25:10 EST