Trehalose conserves expression of bullous pemphigoid antigen 180 during desiccation and freezing

Enno Schmidt, Arno Kromminga, Markus Kürschner, Heiko Zimmermann, Alisa D. Katsen, Eva Bettina Bröcker, Detlef Zillikens, Ulrich Zimmermann*, Vladimir L. Sukhorukov

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

Bullous pemphigoid antigen 180 (BP180) is targeted by autoantibodies in a variety of subepidermal blistering skin diseases. We have recently developed a simple, highly specific and sensitive immunofluorescence (IF) assay for the detection of circulating antibodies against BP180. This novel assay involves the expression of full-length (FL) BP180 in Sf21 insect cells that are then examined under IF microscopy after staining with anti-BP180 antibodies. Application of this assay as a routine diagnostic tool requires long-term storage of FL-BP180, which can result in substantial loss of expression. Here, we show that the disaccharide trehalose, a natural cryo- and lyoprotectant, is capable of preserving the FL-BP180 antigen expressed in Sf21 insect cells under various (dry) storage conditions including 40°C, room temperature (RT), 4-8, -20, and -80°C. The protective effect was dose-dependent reaching a maximum at about 200 mM trehalose. Trehalose was superior to other sugars or conventional cryoprotective agents (e.g. sucrose, myo-inositol, DMSO) in preventing greatly reduced antigen expression. Trehalose conserved the expression of both extra- and intracellular epitopes of FL-BP180. Interestingly, protection of the intracellular domain was only observed when trehalose was introduced into the cytosol. Trehalose significantly prolonged the storage time of FL-BP180 expressed in Sf21 insect cells, thus permitting the routine use of the IF assay in clinics for the detection of serum antibodies. The method described here has potential applications for the preservation of other transmembrane proteins.

OriginalspracheEnglisch
ZeitschriftJournal of Immunological Methods
Jahrgang275
Ausgabenummer1-2
Seiten (von - bis)179-190
Seitenumfang12
ISSN0022-1759
DOIs
PublikationsstatusVeröffentlicht - 01.04.2003

Fördermittel

This work was supported by grants from the Bundesministerium für Bildung und Forschung (BMBF-16SV1329/0 to U.Z., BMBF-16SV1366/0 and BMBF-13N8081 to Fraunhofer-IBMT) and the Interdisciplinary Center for Clinical Research at the University of Würzburg, Germany (IZKF-01KS9603 to E.S.). We thank Dr. Katshushi Owaribe, Nagoya, Japan for providing us with monoclonal antibodies 233 and 1A8c to BP180. We thank Dr. Stephen G. Shirley for carefully proof reading and Susan Pflüger for the technical assistance.

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

  • Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)

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