Development of a single-chain variable fragment-alkaline phosphatase fusion protein and a sensitive direct competitive chemiluminescent enzyme immunoassay for detection of ractopamine in pork

2012 ◽  
Vol 736 ◽  
pp. 85-91 ◽  
Author(s):  
Jie-Xian Dong ◽  
Zhen-Feng Li ◽  
Hong-Tao Lei ◽  
Yuan-Ming Sun ◽  
Frédéric Ducancel ◽  
...  
Keyword(s):  
Alkaline Phosphatase ◽  
Fusion Protein ◽  
Enzyme Immunoassay ◽  
Single Chain Variable Fragment ◽  
Single Chain ◽  
Chemiluminescent Enzyme Immunoassay

Construction of Single Chain Variable Fragment (ScFv) and BiscFv-Alkaline Phosphatase Fusion Protein for Detection ofBacillusAnthracis

2006 ◽  
Vol 78 (4) ◽  
pp. 997-1004 ◽  
Author(s):  
Shi-Hua Wang ◽  
Ji-Bin Zhang ◽  
Zhi-Ping Zhang ◽  
Ya-Feng Zhou ◽  
Rui-Fu Yang ◽  
...  
Keyword(s):  
Alkaline Phosphatase ◽  
Fusion Protein ◽  
Single Chain Variable Fragment ◽  
Single Chain

Production and characterization of a single-chain variable fragment-alkaline phosphatase fusion protein for glycocholic acid detection in a one-step enzyme-linked immunosorbent assay

2018 ◽  
Vol 10 (22) ◽  
pp. 2629-2635 ◽  
Author(s):  
Xiping Cui ◽  
Qiyi He ◽  
Ding Shen ◽  
Zhengyun Jiang ◽  
Yingshan Chen ◽  
...  
Keyword(s):  
Alkaline Phosphatase ◽  
Fusion Protein ◽  
Immunosorbent Assay ◽  
Enzyme Linked Immunosorbent Assay ◽  
Single Chain Variable Fragment ◽  
Single Chain ◽  
Glycocholic Acid ◽  
One Step

One-step enzyme-linked immunosorbent assay for glycocholic acid based on single-chain variable fragment-alkaline phosphatase fusion protein.

scholarly journals An Affibody Molecule Is Actively Transported into the Cerebrospinal Fluid via Binding to the Transferrin Receptor

2020 ◽  
Vol 21 (8) ◽  
pp. 2999
Author(s):  
Sebastian W. Meister ◽  
Linnea C. Hjelm ◽  
Melanie Dannemeyer ◽  
Hanna Tegel ◽  
Hanna Lindberg ◽  
...  
Keyword(s):  
Cerebrospinal Fluid ◽  
Fusion Protein ◽  
Transferrin Receptor ◽  
Preclinical Study ◽  
Single Chain Variable Fragment ◽  
Target Engagement ◽  
Single Chain ◽  
Affibody Molecule ◽  
The Central Nervous System ◽  
Binding Antibody

The use of biotherapeutics for the treatment of diseases of the central nervous system (CNS) is typically impeded by insufficient transport across the blood–brain barrier. Here, we investigate a strategy to potentially increase the uptake into the CNS of an affibody molecule (ZSYM73) via binding to the transferrin receptor (TfR). ZSYM73 binds monomeric amyloid beta, a peptide involved in Alzheimer’s disease pathogenesis, with subnanomolar affinity. We generated a tri-specific fusion protein by genetically linking a single-chain variable fragment of the TfR-binding antibody 8D3 and an albumin-binding domain to the affibody molecule ZSYM73. Simultaneous tri-specific target engagement was confirmed in a biosensor experiment and the affinity for murine TfR was determined to 5 nM. Blockable binding to TfR on endothelial cells was demonstrated using flow cytometry and in a preclinical study we observed increased uptake of the tri-specific fusion protein into the cerebrospinal fluid 24 h after injection.

Chemiluminescent enzyme immunoassay of alpha-fetoprotein based on an adamantyl dioxetane phenyl phosphate substrate.

1989 ◽  
Vol 35 (12) ◽  
pp. 2319-2321 ◽  
Author(s):  
G H Thorpe ◽  
I Bronstein ◽  
L J Kricka ◽  
B Edwards ◽  
J C Voyta
Keyword(s):  
Alkaline Phosphatase ◽  
Enzyme Immunoassay ◽  
Detection Limits ◽  
Alpha Fetoprotein ◽  
Phenyl Phosphate ◽  
Comparison Of Results ◽  
Enzyme Detection ◽  
Chemiluminescent Enzyme Immunoassay

Abstract We have evaluated a new chemiluminescent substrate for the alkaline phosphatase (EC 3.1.3.1) label used in a Hybritech Tandem-E immunoassay of alpha-fetoprotein (AFP). The new substrate, adamantyl 1,2-dioxetane phenyl phosphate (AMPPD), emits light at 477 nm when acted upon by the enzyme. Detection limits for AFP with this method were 33 ng/L (mean of 20 replicates of the zero standard + 2 SD) and 470 ng/L (twice background). Between-batch CVs ranged from 4.31% to 9.60% for AFP in the range 29.1-132.0 micrograms/L. Comparison of results for 49 specimens assayed with use of the chemiluminescent kit and a colorimetric version of the AFP assay gave statistical values as follows: slope = 0.88, intercept = 4.19, and r = 0.94.

Chemiluminescence competitive indirect enzyme immunoassay for 20 fluoroquinolone residues in fish and shrimp based on a single-chain variable fragment

2013 ◽  
Vol 405 (23) ◽  
pp. 7477-7484 ◽  
Author(s):  
Xiaoqi Tao ◽  
Min Chen ◽  
Haiyang Jiang ◽  
Jianzhong Shen ◽  
Zhanhui Wang ◽  
...  
Keyword(s):  
Enzyme Immunoassay ◽  
Single Chain Variable Fragment ◽  
Single Chain

scholarly journals Screening Antibody Libraries with Colony Assay Using scFv-Alkaline Phosphatase Fusion Proteins

Molecules ◽  
2020 ◽  
Vol 25 (12) ◽  
pp. 2905
Author(s):  
Yoshiro Hanyu ◽  
Mieko Kato
Keyword(s):  
Alkaline Phosphatase ◽  
Fusion Proteins ◽  
Direct Detection ◽  
Screening Methods ◽  
Single Chain Variable Fragment ◽  
Antibody Library ◽  
Single Chain ◽  
Library Size ◽  
Colony Assay ◽  
Antibody Libraries

Screening antibody libraries is an important step in establishing recombinant monoclonal antibodies. The colony assay can identify positive clones without almost any false-positives; however, its antibody library is smaller than those used in other recombinant screening methods such as phage display. Thus, to improve the efficiency of colony assays, it is necessary to increase library size per screening. Here, we report developing a colony assay with single-chain variable fragment (scFv) fused to the N-terminus of bacterial alkaline phosphatase (scFv-PhoA). The scFv-PhoA library was constructed in an expression vector specifically designed for this study. Use of this library allowed the successful and direct detection of positive clones exhibiting PhoA activity, without the need for a secondary antibody. Colony assay screening with scFv-PhoA is simple, rapid, offers a higher success rate than previous methods based on scFv libraries, and—most importantly—it enables high-throughput procedures.

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