Evaluation of homo- and hetero-functionally activated glass surfaces for optimized antibody arrays

被引:22
作者
Gonzalez-Gonzalez, Maria [1 ,2 ]
Bartolome, Raquel [1 ,2 ]
Jara-Acevedo, Ricardo [3 ]
Casado-Vela, Juan [4 ]
Dasilva, Noelia [1 ,2 ]
Matarraz, Sergio [1 ,2 ]
Garcia, Jacinto [5 ]
Alcazar, J. A. [5 ]
Sayagues, J. M. [1 ,2 ]
Orfao, Alberto [1 ,2 ]
Fuentes, Manuel [1 ,2 ]
机构
[1] Univ Salamanca, Dept Med, Ctr Invest Canc IBMCC USAL CSIC IBSAL, Salamanca 37007, Spain
[2] Univ Salamanca, Serv Gen Citometria, Salamanca 37007, Spain
[3] ImmunoStep, Salamanca 37007, Spain
[4] CSIC, Spanish Natl Biotechnol Ctr CNB, Madrid 28049, Spain
[5] Hosp Clin Univ Salamanca IBSAL, Serv Cirugia, Salamanca 37007, Spain
关键词
Antibody arrays; Surface functionalization; Antibody immobilization; Protein microarrays; Functionalized surfaces; PROTEIN MICROARRAYS; IMMOBILIZATION; CHEMISTRIES; TECHNOLOGY; INERT;
D O I
10.1016/j.ab.2014.01.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Antibody arrays hold great promise for biomedical applications, but they are typically manufactured using chemically functionalized surfaces that still require optimization. Here, we describe novel hetero-functionally activated glass surfaces favoring oriented antibody binding for improved performance in protein microarray applications. Antibody arrays manufactured in our facility using the functionalization chemistries described here proved to be reproducible and stable and also showed good signal intensities. As a proof-of-principle of the glass surface functionalization protocols described in this article, we built antibody-based arrays functionalized with different chemistries that enabled the simultaneous detection of 71 human leukocyte membrane differentiation antigens commonly found in peripheral blood mononuclear cells. Such detection is specific and semi-quantitative and can be performed in a single assay under native conditions. In summary, the protocol described here, based on the use of antibody array technology, enabled the concurrent detection of a set of membrane proteins under native conditions in a specific, selective, and semi-quantitative manner and in a single assay. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:37 / 45
页数:9
相关论文
共 29 条
[1]   Preparation of DNA and protein micro arrays on glass slides coated with an agarose film [J].
Afanassiev, Victor ;
Hanemann, Vera ;
Woelfl, Stefan .
NUCLEIC ACIDS RESEARCH, 2000, 28 (12) :E66
[2]   Oriented covalent immobilization of antibodies on physically inert and hydrophilic support surfaces through their glycosidic chains [J].
Batalla, Pilar ;
Fuentes, Manuel ;
Grazu, Valeria ;
Mateo, Cesar ;
Fernandez-Lafuente, Roberto ;
Guisan, Jose M. .
BIOMACROMOLECULES, 2008, 9 (02) :719-723
[3]  
Belov L, 2001, CANCER RES, V61, P4483
[4]   Design of high-density antibody microarrays for disease proteomics: Key technological issues [J].
Borrebaeck, Carl A. K. ;
Wingren, Christer .
JOURNAL OF PROTEOMICS, 2009, 72 (06) :928-935
[5]  
Chung Alicia S., 2009, V527, P247, DOI 10.1007/978-1-60327-834-8_18
[6]  
Diez Paula, 2012, Microarrays (Basel), V1, P64, DOI 10.3390/microarrays1020064
[7]   Multiplex detection of surface molecules on colorectal cancers [J].
Ellmark, P ;
Belov, L ;
Huang, P ;
Lee, CS ;
Solomon, MJ ;
Morgan, DK ;
Christopherson, RI .
PROTEOMICS, 2006, 6 (06) :1791-1802
[8]   Preparation of inert magnetic nano-particles for the directed immobilization of antibodies [J].
Fuentes, M ;
Mateo, C ;
Guisán, JM ;
Fernández-Lafuente, R .
BIOSENSORS & BIOELECTRONICS, 2005, 20 (07) :1380-1387
[9]   Nanotechniques in proteomics: Protein microarrays and novel detection platforms [J].
Gonzalez-Gonzalez, Maria ;
Jara-Acevedo, Ricardo ;
Matarraz, Sergio ;
Jara-Acevedo, Maria ;
Paradinas, Sara ;
Sayaguees, J. M. ;
Orfao, Alberto ;
Fuentes, Manuel .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2012, 45 (04) :499-506
[10]   Antibody microarrays: An evaluation of production parameters [J].
Kusnezow, W ;
Jacob, A ;
Walijew, A ;
Diehl, F ;
Hoheisel, JD .
PROTEOMICS, 2003, 3 (03) :254-264