Refolding of autodisplayed anti-NEF scFv through oxidation with glutathione for immunosensors

Title
Refolding of autodisplayed anti-NEF scFv through oxidation with glutathione for immunosensors
Authors
강민정봉지홍송현우김태훈요아힘 요세변재철
Keywords
Negative regulatory factor (NEF); Autodisplay; Single-chain variable fragment (scFv); Glutathione; Immunoassay
Issue Date
2018-04
Publisher
Biosensors and bioelectronics
Citation
VOL 102-609
Abstract
In this study, a single-domain antibody against negative regulatory factor (anti-NEF scFv) was autodisplayed on the outer membrane of Escherichia colt and used to detect NEF in an immunoassay based on fluorescence-activated cell sorting, enzyme-linked immunosorbent assay, and surface plasmon resonance biosensors. Next, the autodisplayed single-domain antibody was oxidized to form disulfide bonds by using glutathione, and the change in NEF-binding activity of anti-NEF scFv was analyzed by fluorescence-activated cell sorting-based immunoassay, chromogenic immunoassay, and surface plasmon resonance biosensor. For each type,of immunoassays the anti-NEF scFv on the isolated outer membrane showed more NEF binding activity after the disulfide bond formation by glutathione. To determine the role of cysteines in anti-NEF scFv, three mutants were prepared, and the NEF binding activity of mutants was compared with that of wild-type anti-NEF scFv in a competitive immunoassay based on FACS. In these mutant studies, the refolding process of autodisplayed anti-NEF scFv by following oxidation via GSH/GSSG revealed that disulfide bonds formed and increased NEF binding activity.
URI
http://pubs.kist.re.kr/handle/201004/67782
ISSN
0956-5663
Appears in Collections:
KIST Publication > Article
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