Isolation and Characterization of Targeting-HBsAg VNAR Single Domain Antibodies from Whitespotted Bamboo Sharks (Chiloscyllium plagiosum)

Author:

Jiang Xierui12,Sun Shan23,Li Zengpeng2,Chen Mingliang24ORCID

Affiliation:

1. School of Advanced Manufacturing, Fuzhou University, Quanzhou 362251, China

2. Key Laboratory of Marine Genetic Resources, State Key Laboratory Breeding Base of Marine Genetic Resources, Fujian Key Laboratory of Marine Genetic Resources, Fujian Collaborative Innovation Centre for Exploitation and Utilization of Marine Biological Resources, Third Institute of Oceanography Ministry of Natural Resources, Xiamen 361005, China

3. Key Laboratory of Ministry of Education for Conservation and Utilization of Special Biological Resources in the Western, Life Science School, Ningxia University, Yinchuan 750021, China

4. Co-Innovation Center of Jiangsu Marine Bio-Industry Technology, Jiangsu Ocean University, Lianyungang 222005, China

Abstract

Immunoglobulin new antigen receptor (IgNAR) is a naturally occurring antibody that consists of only two heavy chains with two independent variable domains. The variable binding domain of IgNAR, called variable new antigen receptor (VNAR), is attractive due to its solubility, thermal stability, and small size. Hepatitis B surface antigen (HBsAg) is a viral capsid protein found on the surface of the Hepatitis B virus (HBV). It appears in the blood of an individual infected with HBV and is widely used as a diagnostic marker for HBV infection. In this study, the whitespotted bamboo sharks (Chiloscyllium plagiosum) were immunized with the recombinant HBsAg protein. Peripheral blood leukocytes (PBLs) of immunized bamboo sharks were further isolated and used to construct a VNAR-targeted HBsAg phage display library. The 20 specific VNARs against HBsAg were then isolated by bio-panning and phage ELISA. The 50% of maximal effect (EC50) of three nanobodies, including HB14, HB17, and HB18, were 4.864 nM, 4.260 nM, and 8.979 nM, respectively. The Sandwich ELISA assay further showed that these three nanobodies interacted with different epitopes of HBsAg protein. When taken together, our results provide a new possibility for the application of VNAR in HBV diagnosis and also demonstrate the feasibility of using VNAR for medical testing.

Funder

Scientific Research Foundation of Third Institute of Oceanography

Natural Science Foundation of Xiamen, China

Deep-Sea Habitats Discovery Project

Outstanding Young Talent Project, the Ministry of Natural Resources of China

Xiamen Southern Oceanographic Centre Project

Science and Technology Project of Fujian Province

Publisher

MDPI AG

Subject

Drug Discovery,Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Pharmaceutical Science

Reference33 articles.

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2. Single domain antibodies: Promising experimental and therapeutic tools in infection and immunity;Wesolowski;Med. Microbiol. Immunol.,2009

3. Structural insights and biomedical potential of IgNAR scaffolds from sharks;Zielonka;mAbs,2015

4. Construction and next-generation sequencing analysis of a large phage-displayed V(NAR) single-domain antibody library from six naïve nurse sharks;Feng;Antib. Ther.,2019

5. The structural analysis of shark IgNAR antibodies reveals evolutionary principles of immunoglobulins;Feige;Proc. Natl. Acad. Sci. USA,2014

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