High density peptide microarrays. In situ synthesis and applications

被引:31
作者
Gao, Xiaolian [1 ]
Pellois, Jean Philippe [1 ]
Na, Younghwa [1 ]
Kim, Younkee [3 ]
Gulari, Erdogan [2 ]
Zhou, Xiaochuan [4 ]
机构
[1] Univ Houston, Dept Chem, Houston, TX 77004 USA
[2] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[3] Xeotron Co, Houston, TX 77054 USA
[4] Atactic Technol Inc, Houston, TX 77054 USA
关键词
antibody binding; digital photolithography; epitope screening; miniaturization; parallel synthesis; peptide chip; peptide microarray; PGA; PGR chemistry; protein binding assay;
D O I
10.1023/B:MODI.0000036233.58271.25
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The technologies enabling the creation of large scale, miniaturized peptide or protein microarrays are emerging. The focuses of this review are the synthesis and applications of peptide and peptidomimetic microarrays, especially the light directed parallel synthesis of individually addressable high density peptide microarrays using a novel photogenerated reagent chemistry and digital photolithography (Gao et al., 1998, J. Am. Chem. Soc. 120, 12698; Pellois et al. 2002, Nat. Biotechnol. 20, 922). Concepts related to the synthesis are discussed, such as the reactions of photogenerated acids in the deprotection step of peptide synthesis or oligonucleotide synthesis, and the applications of high density peptide chips in antibody binding assays are discussed. Peptide chips provide versatile tools for probing antigen-antibody, protein-protein, peptide-ligand interactions and are basic components for miniaturization, automation, and system integration in research and clinical diagnosis applications.
引用
收藏
页码:177 / 187
页数:11
相关论文
共 83 条
  • [1] Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling
    Alizadeh, AA
    Eisen, MB
    Davis, RE
    Ma, C
    Lossos, IS
    Rosenwald, A
    Boldrick, JG
    Sabet, H
    Tran, T
    Yu, X
    Powell, JI
    Yang, LM
    Marti, GE
    Moore, T
    Hudson, J
    Lu, LS
    Lewis, DB
    Tibshirani, R
    Sherlock, G
    Chan, WC
    Greiner, TC
    Weisenburger, DD
    Armitage, JO
    Warnke, R
    Levy, R
    Wilson, W
    Grever, MR
    Byrd, JC
    Botstein, D
    Brown, PO
    Staudt, LM
    [J]. NATURE, 2000, 403 (6769) : 503 - 511
  • [2] Genomic interrogation of mechanism(s) underlying cellular responses to toxicants
    Amin, RP
    Hamadeh, HK
    Bushel, PR
    Bennett, L
    Afshari, CA
    Paules, RS
    [J]. TOXICOLOGY, 2002, 181 : 555 - 563
  • [3] BECKSICKINGER AG, 1996, COMBINATORIAL PEPTID, P79
  • [4] BEECHER JE, 1997, POLYM MAT SCI ENG, V76, P394
  • [5] Analysis of DNA-microarrays produced by inverse in situ oligonucleotide synthesis
    Beier, M
    Hoheisel, JD
    [J]. JOURNAL OF BIOTECHNOLOGY, 2002, 94 (01) : 15 - 22
  • [6] Beier M, 2000, Nucleic Acids Res, V28, pE11, DOI 10.1093/nar/28.4.e11
  • [7] BIALEK K, 2003, ANAL BIOANAL CHEM
  • [8] Total synthesis of distamycin A and 2640 analogues: A solution-phase combinatorial approach to the discovery of new, bioactive DNA binding agents and development of a rapid, high-throughput screen for determining relative DNA binding affinity or DNA binding sequence selectivity
    Boger, DL
    Fink, BE
    Hedrick, MP
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (27) : 6382 - 6394
  • [9] SH3-SPOT: An algorithm to predict preferred ligands to different members of the SH3 gene family
    Brannetti, B
    Via, A
    Cestra, G
    Cesareni, G
    Citterich, MH
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2000, 298 (02) : 313 - 328
  • [10] Proteome-scale purification of human proteins from bacteria
    Braun, P
    Hu, YH
    Shen, BH
    Halleck, A
    Koundinya, M
    Harlow, E
    LaBaer, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (05) : 2654 - 2659