Production and characterization of domain-specific monoclonal antibodies against human ECM1

被引:2
作者
Li, Ya [1 ]
Li, Yanqing [1 ]
Zhao, Junli [1 ]
Wang, Dongyang [1 ]
Mao, Qinwen [2 ]
Xia, Haibin [1 ]
机构
[1] Shaanxi Normal Univ, Coll Life Sci, Coinnovat Ctr Qinba Reg Sustainable Dev, 199 South Changan Rd, Xian 710062, Shaanxi, Peoples R China
[2] Northwestern Univ, Dept Pathol, Feinberg Sch Med, 303 E Chicago Ave, Chicago, IL 60611 USA
基金
中国国家自然科学基金;
关键词
ECM1; Monoclonal antibody; Hybridoma; Prokaryotic expression; EXTRACELLULAR-MATRIX PROTEIN-1; LIPOID PROTEINOSIS; LYMPHATIC METASTASIS; GENE; MUTATION; EXPRESSION; IDENTIFICATION; INTERACTS; FAMILIES; INVASION;
D O I
10.1016/j.pep.2016.01.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Human extracellular matrix protein-1 (hECM1), a secreted glycoprotein, is widely expressed in different tissues and organs. ECM1 has been implicated in multiple biological functions, which are potentially mediated by the interaction of different ECM1 domains with its ligands. However, the exact biological functions of ECM1 have not been elucidated yet, and the functional study of ECM1 has been partially hampered by the lack of sensitive and specific antibodies, especially those targeting different ECM1 domains. In this study, six strains of monoclonal antibody (MAb) against hECM1 were generated using purified, prokaryotically-expressed hECM1 as an immunogen. The MAbs were shown to be highly sensitive and specific, and suitable for western blot, immunoprecipitation assays and immunohistochemistry. Furthermore, the particular ECM1 domains recognized by different MAbs were identified. Lastly, the MAbs were found to have neutralizing activities, inhibiting the proliferation, migration and metastasis of MDA-MB-231 cells. In conclusion, the domain-specific anti-ECM1 MAbs produced in this study should provide a useful tool for investigating ECM1's biological functions, and cellular pathways in which it is involved. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:103 / 111
页数:9
相关论文
共 35 条
  • [1] A novel splice-site ECM1 gene mutation in a Lebanese girl with lipoid proteinosis
    Abbas, Ossama
    Farooq, Muhammad
    El Khoury, Jinane
    Kibbi, Abdul-Ghani
    Fujikawa, Hiroki
    Fujimoto, Atsushi
    Shimomura, Yutaka
    Kurban, Mazen
    [J]. INTERNATIONAL JOURNAL OF DERMATOLOGY, 2013, 52 (07) : 824 - 826
  • [2] MOLECULAR-CLONING, CHARACTERIZATION, AND GENETIC-MAPPING OF THE CDNA CODING FOR A NOVEL SECRETORY PROTEIN OF MOUSE - DEMONSTRATION OF ALTERNATIVE SPLICING IN SKIN AND CARTILAGE
    BHALERAO, J
    TYLZANOWSKI, P
    FILIE, JD
    KOZAK, CA
    MERREGAERT, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (27) : 16385 - 16394
  • [3] Extracellular matrix protein 1, a novel prognostic factor, is associated with metastatic potential of hepatocellular carcinoma
    Chen, Hao
    Jia, Wei-Dong
    Li, Jian-Sheng
    Wang, Wei
    Xu, Ge-Liang
    Ma, Jin-Liang
    Ren, Wei-Hua
    Ge, Yong-Sheng
    Yu, Ji-Hai
    Liu, Wen-Bin
    Zhang, Chuan-Hai
    Wang, Yong-Cang
    [J]. MEDICAL ONCOLOGY, 2011, 28 : S318 - S325
  • [4] Recombinant human extracellular matrix protein 1 inhibits alkaline phosphatase activity and mineralization of mouse embryonic metatarsals in vitro
    Deckers, MML
    Smits, P
    Karperien, M
    Ni, J
    Tylzanowski, P
    Feng, P
    Parmelee, D
    Zhang, J
    Bouffard, E
    Gentz, R
    Löwik, CWG
    Merregaert, J
    [J]. BONE, 2001, 28 (01) : 14 - 20
  • [5] PRODUCTION OF MONOCLONAL-ANTIBODIES - STRATEGY AND TACTICS
    DESTGROTH, SF
    SCHEIDEGGER, D
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1980, 35 (1-2) : 1 - 21
  • [6] Extracellular matrix protein 1 inhibits the activity of matrix metalloproteinase 9 through high-affinity protein/protein interactions
    Fujimoto, N
    Terlizzi, J
    Aho, S
    Brittingham, R
    Fertala, A
    Oyama, N
    McGrath, JA
    Uitto, J
    [J]. EXPERIMENTAL DERMATOLOGY, 2006, 15 (04) : 300 - 307
  • [7] Extracellular matrix protein 1 interacts with the domain III of fibulin-1C and 1D variants through its central tandem repeat 2
    Fujimoto, N
    Terlizzi, J
    Brittingham, R
    Fertala, A
    McGrath, JA
    Uitto, J
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 333 (04) : 1327 - 1333
  • [8] Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation
    Hamada, T
    Wessagowit, V
    South, AP
    Ashton, GHS
    Chan, I
    Oyama, N
    Siriwattana, A
    Jewhasuchin, P
    Charuwichitratana, S
    Thappa, DM
    Lenane, P
    Krafchik, B
    Kulthanan, K
    Shimizu, H
    Kaya, TI
    Erdal, ME
    Paradisi, M
    Paller, AS
    Seishima, M
    Hashimoto, T
    McGrath, AA
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (03) : 345 - 350
  • [9] Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1)
    Hamada, T
    McLean, WHI
    Ramsay, M
    Ashton, GHS
    Nanda, A
    Jenkins, T
    Edelstein, I
    South, AP
    Bleck, O
    Wessagowit, V
    Mallipeddi, R
    Orchard, GE
    Wan, H
    Dopping-Hepenstal, PJC
    Mellerio, JE
    Whittock, NV
    Munro, CS
    van Steensel, MAM
    Steijlen, PM
    Ni, J
    Zhang, LR
    Hashimoto, T
    Eady, RAJ
    McGrath, JA
    [J]. HUMAN MOLECULAR GENETICS, 2002, 11 (07) : 833 - 840
  • [10] The Relationship between the Extracellular Matrix and the Angiogenesis and Metastasis of Laryngeal Carcinoma
    Han, Zhao
    Lin, Guo-Jing
    Chi, Fang-Lu
    Wang, Shu-Yi
    Huang, Jian-Min
    Liu, Hong-Jian
    Zhang, Lu-Rong
    [J]. ORL-JOURNAL FOR OTO-RHINO-LARYNGOLOGY AND ITS RELATED SPECIALTIES, 2008, 70 (06): : 352 - 358