Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

We have developed a quantitative assay for the measurement of class I assembly induced by peptide. We have applied this assay to H-2Db, Kb and HLA-A2.1 with a panel of 49 overlapping peptides derived from HIV-1 gag protein. We find that the effects of peptide on assembly form a continuous distribution. By defining positives as those that increase the concentration of folded heavy chains more than three standard deviations from the control we show that 7/48 bind A2.1, 11/49 bind Db and 7/47 bind Kb. The assembly assay contrasts with solid-phase assays in being more discriminating (fewer peptides binding any given class I molecule), and showing less overlap in the patterns of peptides bound by the three class I molecules.

Original publication

DOI

10.1002/eji.1830210909

Type

Journal article

Journal

Eur J Immunol

Publication Date

09/1991

Volume

21

Pages

2025 - 2031

Keywords

Amino Acid Sequence, Electrophoresis, Polyacrylamide Gel, Gene Products, gag, H-2 Antigens, HLA-A2 Antigen, Histocompatibility Antigens Class I, Humans, Immunoglobulin Heavy Chains, Lymphoma, Molecular Sequence Data, Precipitin Tests, Tumor Cells, Cultured, beta 2-Microglobulin