A comprehensive approach for establishment of the platform to analyze functions of KIAA proteins: Generation and evaluation of anti-mKIAA antibodies

被引:19
作者
Koga, H
Shimada, K
Hara, Y
Nagan, M
Kohga, H
Yokoyama, R
Kimura, Y
Yuasa, S
Magae, J
Inamoto, S
Okazaki, N
Ohara, O
机构
[1] Kazusa DNA Res Inst, Chiba 2920818, Japan
[2] Chiba Ind Adv Ctr, Chiba, Japan
[3] RIKEN Yokohama Inst, Kanagawa, Japan
[4] Natl Inst Neurosci, Tokyo, Japan
[5] Inst Res & Innovat, Chiba, Japan
关键词
antibody; high-throughput; mass spectrometry; mKIAA; mouse;
D O I
10.1002/pmic.200300704
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Since December 2001 we have been conducting a project to isolate and determine entire sequences of mouse KIAA cDNA clones which encode polypeptides corresponding to human KIAA proteins. The ultimate goal of this project is the elucidation of the functions of KIAA proteins. A critical step in this project is the generation of antibodies based on the cDNA sequence information. Although antibodies are the most optimal tools for biological analysis, the production and isolation of multiple recombinant proteins for an antigen is a rate-limiting step in antibody production. To address this problem, we established a system utilizing the in vitro recombination-assisted method and shotgun clones that were generated during the sequencing of mouse KIAA cDNAs; (DNA Res. 2003, 10, 129-136). The authenticity of the expressed proteins was confirmed by matrix-assisted laser desorption/ionization-time of flight mass spectrometry. Another critical step for antibody production is the evaluation of the antibodies. Thus, we also made efforts to develop a systematic approach for evaluation of the titer and the specificity of the antibodies. Using these systems, we have produced and evaluated more than 500 antibodies raised against mouse KIAA proteins to date. We are currently generating antibody arrays for analysis of protein expression profiles. We will verify protein-protein interactions using immunoprecipitation and tandem mass spectrometry analysis.
引用
收藏
页码:1412 / 1416
页数:5
相关论文
共 16 条
[1]   Affinity proteomics for systematic protein profiling of chromosome 21 gene products in human tissues [J].
Agaton, C ;
Galli, J ;
Guthenberg, IH ;
Janzon, L ;
Hansson, M ;
Asplund, A ;
Brundell, E ;
Lindberg, S ;
Ruthberg, I ;
Wester, K ;
Wurtz, D ;
Höög, C ;
Lundeberg, J ;
Ståhl, S ;
Pontén, F ;
Uhlén, M .
MOLECULAR & CELLULAR PROTEOMICS, 2003, 2 (06) :405-414
[2]   High-throughput production of recombinant antigens for mouse KIAA proteins in Escherichia coli:: Computational allocation of possible antigenic regions, and construction of expression plasmids of glutathione-S-transferase-fused antigens by an in vitro recombination-assisted method [J].
Hara, Y ;
Shimada, I ;
Kohga, H ;
Ohara, O ;
Koga, H .
DNA RESEARCH, 2003, 10 (03) :129-136
[3]  
Harder A, 1999, ELECTROPHORESIS, V20, P826, DOI 10.1002/(SICI)1522-2683(19990101)20:4/5<826::AID-ELPS826>3.0.CO
[4]  
2-A
[5]   Transcriptional squelching by ectopic expression of E2F-1 and p53 is alleviated by proteasome inhibitors MG-132 and lactacystin [J].
Magae, J ;
Illenye, S ;
Tejima, T ;
Chang, YC ;
Mitsui, Y ;
Tanaka, K ;
Omura, S ;
Heintz, NH .
ONCOGENE, 1997, 15 (07) :759-769
[6]   Positionally cloned human disease genes: Patterns of evolutionary conservation and functional motifs [J].
Mushegian, AR ;
Bassett, DE ;
Boguski, MS ;
Bork, P ;
Koonin, EV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (11) :5831-5836
[7]  
Nakajima D, 2002, DNA RES, V9, P99, DOI 10.1093/dnares/9.3.99
[8]  
Nomura N, 1994, DNA Res, V1, P27, DOI 10.1093/dnares/1.1.27
[9]  
Oh-Ishi M, 2000, ELECTROPHORESIS, V21, P1653, DOI 10.1002/(SICI)1522-2683(20000501)21:9<1653::AID-ELPS1653>3.0.CO
[10]  
2-9