| Literature DB >> 25758251 |
Xiaofang Bian1, Peter Wiktor2, Peter Kahn3, Al Brunner3, Amritpal Khela1, Kailash Karthikeyan1, Kristi Barker1, Xiaobo Yu1, Mitch Magee1, Clive H Wasserfall4, David Gibson5, Madeleine E Rooney6, Ji Qiu1, Joshua LaBaer1.
Abstract
Viral infections elicit antiviral antibodies and have been associated with various chronic diseases. Detection of these antibodies can facilitate diagnosis, treatment of infection, and understanding of the mechanisms of virus-associated diseases. In this work, we assayed antiviral antibodies using a novel high-density nucleic acid programmable protein array (HD-NAPPA) platform. Individual viral proteins were expressed in situ directly from plasmids encoding proteins in an array of microscopic reaction chambers. Quality of protein display and serum response was assured by comparing intra- and inter-array correlation within or between printing batches with average correlation coefficients of 0.91 and 0.96, respectively. HD-NAPPA showed higher signal-to-background ratio compared with standard NAPPA on planar glass slides and ELISA. Antibody responses to 761 antigens from 25 different viruses were profiled among patients with juvenile idiopathic arthritis and type 1 diabetes. Common and unique antibody reactivity patterns were detected between patients and healthy controls. We believe HD-viral-NAPPA will enable the study of host-pathogen interactions at unprecedented dimensions and elucidate the role of pathogen infections in disease development.Entities:
Keywords: Antiviral antibodies; HD-NAPPA; Juvenile idiopathic arthritis; Protein arrays; Type 1 diabetes
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Year: 2015 PMID: 25758251 PMCID: PMC4545592 DOI: 10.1002/pmic.201400612
Source DB: PubMed Journal: Proteomics ISSN: 1615-9853 Impact factor: 3.984