| Literature DB >> 28637250 |
Kyohei Yumura1, Hiroki Akiba2, Satoru Nagatoishi2, Osamu Kusano-Arai3, Hiroko Iwanari3, Takao Hamakubo3, Kouhei Tsumoto1,2,4.
Abstract
Bispecific antibody targeting of two different antigens is promising, but when fragment-based antibodies are used, homogeneous production is difficult. To overcome this difficulty, we developed a method using the SpyTag/SpyCatcher system in which a covalent bond is formed between the two polypeptides. Using this method, we constructed a bispecific antibody that simultaneously interacted with two different epitopes of roundabout homologue 1 (ROBO1), a membrane protein associated with cancer progression. A bispecific tetravalent antibody with an additional functional moiety was also constructed by using a dimeric biotin-binding protein. An interaction analysis of ROBO1-expressing cells and the recombinant antigen demonstrated the improved binding ability of the bispecific antibodies through spontaneous binding of the two antibody fragments to their respective epitopes. In addition, multivalency delayed dissociation, which is advantageous in therapy and diagnosis.Entities:
Keywords: SpyTag; biolayer interferometry; bispecific antibody; isothermal titration calorimetry; single-chain Fv
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Year: 2017 PMID: 28637250 DOI: 10.1093/jb/mvx023
Source DB: PubMed Journal: J Biochem ISSN: 0021-924X Impact factor: 3.387