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Activity profile of dust mite allergen extract using substrate libraries and functional proteomic microarrays

Harris, Jennifer; Mason, Daniel E.; Li, Jun; Burdick, Keith W.; Backes, Bradley J.; Chen, Teresa; Shipway, Aaron; Van Heeke, Gino; Gough, Lucy; Ghaemmaghami, Amir; Shakib, Farouk; Debaene, François; Winssinger, Nicolas

Authors

Jennifer Harris

Daniel E. Mason

Jun Li

Keith W. Burdick

Bradley J. Backes

Teresa Chen

Aaron Shipway

Gino Van Heeke

Farouk Shakib

François Debaene

Nicolas Winssinger



Abstract

Enzymatic activity in the fecal droppings from the house dust mite has been postulated to contribute to the elicited allergic response. Screening dust mite extracts through 137,180 tetrapeptide fluorogenic substrates allowed for the characterization of proteolytic substrate specificity from the potential cysteine and serine proteases in the extract. The extract was further screened against a 4000 member peptide nucleic acid (PNA) encoded inhibitor library designed to target cysteine proteases using microarray detection. Affinity chromatography coupled with mass spectrometry identified Der p 1 as one of the proteases targeted by the PNA inhibitors in the dust mite lysate. A phenotypic readout of Der p 1 function in allergy progression was demonstrated by the inhibition of CD25 cleavage from T cells by dust mite extract that had been treated with the Der p 1 inhibitor identified from the PNA-encoded inhibitor library.

Journal Article Type Article
Acceptance Date Aug 2, 2004
Online Publication Date Oct 15, 2004
Publication Date Oct 1, 2004
Deposit Date Jan 3, 2023
Journal Cell Chemical Biology
Electronic ISSN 2451-9448
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 11
Issue 10
Pages 1361-1372
DOI https://doi.org/10.1016/j.chembiol.2004.08.008
Public URL https://nottingham-repository.worktribe.com/output/3097637
Publisher URL https://www.cell.com/cell-chemical-biology/fulltext/S1074-5521(04)00233-9?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1074552104002339%3Fshowall%3Dtrue