Automated Maskless Photolithography System for Peptide Microarray Synthesis on a Chip

被引:21
作者
Shin, Dong-Sik [1 ]
Lee, Kook-Nyung [2 ]
Yoo, Byung-Wook [2 ]
Kim, Jaehi [1 ]
Kim, Mira [1 ]
Kim, Yong-Kweon [2 ]
Lee, Yoon-Sik [1 ]
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 151744, South Korea
[2] Seoul Natl Univ, Sch Elect Engn & Comp Sci, Seoul 151744, South Korea
来源
JOURNAL OF COMBINATORIAL CHEMISTRY | 2010年 / 12卷 / 04期
关键词
HIGH-THROUGHPUT; MICROMIRROR ARRAY; OLIGONUCLEOTIDE MICROARRAYS; SUBSTRATE-SPECIFICITY; PHOTOGENERATED ACID; SPOT SYNTHESIS; FABRICATION; BIOLOGY; LIBRARY; SURFACE;
D O I
10.1021/cc100009g
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Maskless photolithographic peptide synthesis was performed on a glass chip using an automated peptide array synthesizer system. The peptide array synthesizer was built in a closed box, which contained optical and fluidic systems. The conditions for peptide synthesis were fully controlled by a computer program. For the peptide synthesis on a glass chip, 20 NVOC-protected amino acids were synthesized. The coupling efficiencies of two model peptide sequences were examined on ACA/APTS and PEG/CHI/GPTS chips. PEG/CHI/GPIS chip gave higher average stepwise yields of GIYWHHY (94%) and YIYGSFK (98%) than those of ACA/APTS chip. To quantify peptide-protein binding affinity, HPQ- or HPM-containing pentapeptides were synthesized on a PEG/CHI/GPTS chip and the binding event of Cy3 labeled-streptavidin was quantified. The peptide sequence of IQHPQ showed highest binding affinity with Cy3 labeled-streptavidin. The results demonstrated that the photolithographic peptide array synthesis method efficiently quantified the binding activities of protein-peptide interactions and it can be used for additional biological assay applications.
引用
收藏
页码:463 / 471
页数:9
相关论文
共 38 条
[1]   Development of peptide microarrays for epitope mapping of antibodies against the human TSH receptor [J].
Andresen, Heiko ;
Zarse, Kim ;
Groetzinger, Carsten ;
Hollidt, Joerg-M. ;
Ehrentreich-Foerster, Eva ;
Bier, Frank F. ;
Kreuzer, Oliver J. .
JOURNAL OF IMMUNOLOGICAL METHODS, 2006, 315 (1-2) :11-18
[2]   Phosphorylation of serine 468 by GSK-3β negatively regulates basal p65 NF-κB activity [J].
Buss, H ;
Dörrie, A ;
Schmitz, ML ;
Frank, R ;
Livingstone, M ;
Resch, K ;
Kracht, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (48) :49571-49574
[3]   Peptide and small molecule microarray for high throughput cell adhesion and functional assays [J].
Falsey, JR ;
Renil, M ;
Park, S ;
Li, SJ ;
Lam, KS .
BIOCONJUGATE CHEMISTRY, 2001, 12 (03) :346-353
[4]   LIGHT-DIRECTED, SPATIALLY ADDRESSABLE PARALLEL CHEMICAL SYNTHESIS [J].
FODOR, SPA ;
READ, JL ;
PIRRUNG, MC ;
STRYER, L ;
LU, AT ;
SOLAS, D .
SCIENCE, 1991, 251 (4995) :767-773
[5]   The SPOT synthesis technique - Synthetic peptide arrays on membrane supports - principles and applications [J].
Frank, R .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 267 (01) :13-26
[6]   In situ synthesis of oligonucleotide microarrays [J].
Gao, XL ;
Gulari, E ;
Zhou, XC .
BIOPOLYMERS, 2004, 73 (05) :579-596
[7]   High throughput substrate specificity profiling of serine and cysteine proteases using solution-phase fluorogenic peptide microarrays [J].
Gosalia, DN ;
Salisbury, CM ;
Ellman, JA ;
Diamond, SL .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (05) :626-636
[8]   Functional peptide arrays for high-throughput chemical biology based applications [J].
Henderson, Graham ;
Bradley, Mark .
CURRENT OPINION IN BIOTECHNOLOGY, 2007, 18 (04) :326-330
[9]   THE USE OF LIGHT-DIRECTED COMBINATORIAL PEPTIDE-SYNTHESIS IN EPITOPE MAPPING [J].
HOLMES, CP ;
ADAMS, CL ;
KOCHERSPERGER, LM ;
MORTENSEN, RB ;
ALDWIN, LA .
BIOPOLYMERS, 1995, 37 (03) :199-211
[10]   Peptide chips for the quantitative evaluation of protein kinase activity [J].
Houseman, BT ;
Huh, JH ;
Kron, SJ ;
Mrksich, M .
NATURE BIOTECHNOLOGY, 2002, 20 (03) :270-274