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Development of Shark Single Domain Antibodies Specific for Human α-Fetoprotein and the Multimerization Strategy in Serum Detection.
Wang, Zheming; Xie, Xiaoxia; He, Zhenyun; Sun, Zhichang; Zhang, Yongli; Mao, Fujing; Pei, Hua; Zhang, Sihang; Hammock, Bruce D; Liu, Xing.
Afiliación
  • Wang Z; School of Food Science and Engineering, Hainan University, Haikou 570228, China.
  • Xie X; School of Food Science and Engineering, Hainan University, Haikou 570228, China.
  • He Z; School of Food Science and Engineering, Hainan University, Haikou 570228, China.
  • Sun Z; School of Food Science and Engineering, Hainan University, Haikou 570228, China.
  • Zhang Y; School of Food Science and Engineering, Hainan University, Haikou 570228, China.
  • Mao F; School of Food Science and Engineering, Hainan University, Haikou 570228, China.
  • Pei H; Department of Clinical Laboratory, The Second Affiliated Hospital of Hainan Medical University, Haikou 570311, China.
  • Zhang S; School of Food Science and Engineering, Hainan University, Haikou 570228, China.
  • Hammock BD; Department of Entomology and Nematology, and UC Davis Comprehensive Cancer Center, University of California, Davis, California 95616, United States.
  • Liu X; School of Food Science and Engineering, Hainan University, Haikou 570228, China.
Anal Chem ; 96(10): 4242-4250, 2024 03 12.
Article en En | MEDLINE | ID: mdl-38408370
ABSTRACT
Sensitive detection of cancer biomarkers can contribute to the timely diagnosis and treatment of diseases. In this study, the whitespotted bamboo sharks were immunized with human α-fetoprotein (AFP), and a phage-displayed variable new antigen receptor (VNAR) single domain antibody library was constructed. Then four unique VNARs (VNAR1, VNAR11, VNAR21, and VNAR25) against AFP were isolated from the library by biopanning for the first time. All of the sequences belong to type II of VNAR, and the VNAR11 was much different from the rest of the three sequences. Then VNAR1 and VNAR11 were selected to fuse with the C4-binding protein α chain (C4bpα) sequence and efficiently expressed in the Escherichia coli system. Furthermore, a VNAR-C4bpα-mediated sandwich chemiluminescence immunoassay (VSCLIA) was developed for the detection of AFP in human serum samples. After optimization, the VSCLIA showed a limit of detection of 0.74 ng/mL with good selectivity and accuracy. Moreover, the results of clinical serum samples detected by the VSCLIA were confirmed by an automatic immunoanalyzer in the hospital, indicating its practical application in actual samples. In conclusion, the novel antibody element VNAR exhibits great potential for immunodiagnosis, and this study also provides a new direction and experimental basis for AFP detection.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tiburones / Anticuerpos de Dominio Único Límite: Animals / Humans Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tiburones / Anticuerpos de Dominio Único Límite: Animals / Humans Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: China