An Isoform of the Oncogenic Splice Variant AIMP2-DX2 Detected by a Novel Monoclonal Antibody

Bibliographic Details
Title: An Isoform of the Oncogenic Splice Variant AIMP2-DX2 Detected by a Novel Monoclonal Antibody
Authors: Dae Gyu Kim, Thi Thu Ha Nguyen, Nam Hoon Kwon, Junsik Sung, Semi Lim, Eun-Joo Kang, Jihye Lee, Woo Young Seo, Arum Kim, Yoon Soo Chang, Hyunbo Shim, Sunghoon Kim
Source: Biomolecules, Vol 10, Iss 6, p 820 (2020)
Publisher Information: MDPI AG, 2020.
Publication Year: 2020
Collection: LCC:Microbiology
Subject Terms: antibody, splice variant, AIMP2-DX2, phage display, diagnostic marker, Microbiology, QR1-502
More Details: AIMP2-DX2, an exon 2-deleted splice variant of AIMP2 (aminoacyl-tRNA synthetase-interacting multifunctional protein 2), is highly expressed in lung cancer and involved in tumor progression in vivo. Oncogenic function of AIMP2-DX2 and its correlation with poor prognosis of cancer patients have been well established; however, the application of this potentially important biomarker to cancer research and diagnosis has been hampered by a lack of antibodies specific for the splice variant, possibly due to the poor immunogenicity and/or stability of AIMP2-DX2. In this study a monoclonal antibody, H5, that specifically recognizes AIMP2-DX2 and its isoforms was generated via rabbit immunization and phage display techniques, using a short peptide corresponding to the exon 1/3 junction sequence as an antigen. Furthermore, based on mutagenesis, limited cleavage, and mass spectrometry studies, it is also suggested that the endogenous isoform of AIMP2-DX2 recognized by H5 is produced by proteolytic cleavage of 33 amino acids from N-terminus and is capable of inducing cell proliferation similarly to the uncleaved protein. H5 monoclonal antibody is applicable to enzyme-linked immunosorbent assay, immunoblot, immunofluorescence, and immunohistochemistry, and expected to be a valuable tool for detecting AIMP2-DX2 with high sensitivity and specificity for research and diagnostic purposes.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 10060820
2218-273X
Relation: https://www.mdpi.com/2218-273X/10/6/820; https://doaj.org/toc/2218-273X
DOI: 10.3390/biom10060820
Access URL: https://doaj.org/article/f3bea71a026e4f46840e14efab5ddd6b
Accession Number: edsdoj.f3bea71a026e4f46840e14efab5ddd6b
Database: Directory of Open Access Journals
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More Details
ISSN:10060820
2218273X
DOI:10.3390/biom10060820
Published in:Biomolecules
Language:English