Development of Single-Chain Antibodies Specific to Lysophosphatidic Acid Receptor 2
- Authors
- 정상택
- Issue Date
- 4월-2018
- Publisher
- WILEY-V C H VERLAG GMBH
- Keywords
- Lysophosphatidic acid receptor 2; P9; Single-chain antibody; Single-chain variable fragment; amphiphilic poly(gamma-glutamate)-ODG
- Citation
- BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.39, no.4, pp.489 - 494
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- BULLETIN OF THE KOREAN CHEMICAL SOCIETY
- Volume
- 39
- Number
- 4
- Start Page
- 489
- End Page
- 494
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/139774
- DOI
- 10.1002/bkcs.11414
- ISSN
- 0253-2964
- Abstract
- Lysophosphatidic acids (LPAs) are ubiquitous serum phospholipids that trigger diverse cellular responses such as cell proliferation, migration, cell survival, and calcium influx. LPA receptors belong to the G-protein coupled receptor (GPCR) family, and seven subtypes of LPA receptors have been identified. Among them, LPA receptor 2 (LPA(2)) is involved in the proliferation and metastasis of ovarian, cervical, and breast cancers. Hence, LPA(2)-specific antagonists or antibodies are considered as potential anticancer therapeutics. To develop antibodies against LPA(2), a recombinant LPA(2) was expressed in Escherichia coli, purified to homogeneity, and immobilized on a solid surface as an active conformation. An M13 phage library displaying single-chain variable fragments (scFvs) of human IgG containing randomized complementarity-determining regions was applied to select LPA(2)-specific scFv clones. After five rounds of biopanning, a few scFv clones which showed specific binding to LPA(2) were identified. Single-chain antibodies (scAbs), which contain the isolated scFvs and C domain, were constructed and expressed in E. coli. The purified scAbs showed specific binding to LPA(2) with K-D values of 200-600 nM.
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