A one-step immunoassay based on switching peptides for diagnosis of porcine epidemic diarrhea virus (PEDV) using screened Fv-antibodies.
Tae-Hun KimJae-Yeon ParkJaeyong JungJeong Soo SungSoonil KwonHyung Eun BaeHyun-Jin ShinMin-Jung KangJoachim JoseJae-Chul PyunPublished in: Journal of materials chemistry. B (2024)
In this study, a one-step immunoassay for porcine epidemic diarrhea virus (PEDV) based on Fv-antibodies and switching peptides was developed, and the assay results of PEDV were obtained by just mixing samples without any further reaction or washing steps. The Fv-antibodies with binding affinity to the spike protein of PEDV were screened from the Fv-antibody library using the receptor-binding domain (RBD) of the spike protein as a screening probe. Screened Fv-antibodies with binding affinities to the RBD antigen were expressed, and the binding constants ( K D ) were calculated to be 83-142 nM. The one-step immunoassay for the detection of PEDV was configured as a displacement immunoassay using a fluorescence-labeled switching peptide. The one-step immunoassay based on switching peptides was performed using PEDV, and the limit of detection (LOD) values for PEDV detection were estimated to be Ct = 39.7-36.4. Compared with the LOD value for a conventional lateral flow immunoassay (Ct = 33.0), the one-step immunoassay showed a remarkably improved LOD for the detection of PEDV. Finally, the interaction between the screened Fv-antibodies and the PEDV RBD was investigated using docking simulations and compared with the amino acid sequences of the receptors on host cells, such as aminopeptidase N (APN) and angiotensin-converting enzyme-2 (ACE-2).
Keyphrases
- label free
- amino acid
- sensitive detection
- loop mediated isothermal amplification
- angiotensin converting enzyme
- binding protein
- real time pcr
- computed tomography
- angiotensin ii
- molecular dynamics
- quantum dots
- magnetic resonance imaging
- induced apoptosis
- dna binding
- cell death
- small molecule
- transcription factor
- high resolution
- high throughput
- cell proliferation
- mass spectrometry
- positron emission tomography
- irritable bowel syndrome
- cell cycle arrest
- single molecule
- genetic diversity