Recent advances in chemical approaches to the study of biological systems

被引:85
作者
Shogren-Knaak, MA [1 ]
Alaimo, PJ
Shokat, KM
机构
[1] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
关键词
chemical genetics; combinatorial chemistry; enzyme inhibitors; protein-protein interactions; unnatural biopolymers;
D O I
10.1146/annurev.cellbio.17.1.405
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A number of novel chemical methods for studying biological systems have recently been developed that provide a means of addressing biological questions not easily studied with other techniques. In this review, examples that highlight the development and use of such chemical approaches are discussed. Specifically, strategies for modulating protein activity or protein-protein interactions using small molecules are presented. In addition, methods for generating and utilizing novel biomolecules (proteins, oligonucleotides, oligosaccharides, and second messengers) are examined.
引用
收藏
页码:405 / 433
页数:33
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共 114 条
  • [1] A new caged Ca2+, azid-1, is far more photosensitive than nitrobenzyl-based chelators
    Adams, SR
    LevRam, V
    Tsien, RY
    [J]. CHEMISTRY & BIOLOGY, 1997, 4 (11): : 867 - 878
  • [2] Redesigning nucleic acids
    Benner, SA
    Battersby, TR
    Eschgfaller, B
    Hutter, D
    Kodra, JT
    Lutz, S
    Arslan, T
    Baschlin, DK
    Blattler, M
    Egli, M
    Hammer, C
    Held, HA
    Horlacher, J
    Huang, Z
    Hyrup, B
    Jenny, TF
    Jurczyk, SC
    Konig, M
    von Krosigk, U
    Lutz, MJ
    MacPherson, LJ
    Moroney, SE
    Muller, E
    Nambiar, KP
    Piccirilli, JA
    Switzer, CY
    Vogel, JJ
    Richert, C
    Roughton, AL
    Schmidt, J
    Schneider, KC
    Stackhouse, J
    [J]. PURE AND APPLIED CHEMISTRY, 1998, 70 (02) : 263 - 266
  • [3] INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING
    BERRIDGE, MJ
    [J]. NATURE, 1993, 361 (6410) : 315 - 325
  • [4] Acquisition of inhibitor-sensitive protein kinases through protein design
    Bishop, AC
    Shokat, KM
    [J]. PHARMACOLOGY & THERAPEUTICS, 1999, 82 (2-3) : 337 - 346
  • [5] A chemical switch for inhibitor-sensitive alleles of any protein kinase
    Bishop, AC
    Ubersax, JA
    Petsch, DT
    Matheos, DP
    Gray, NS
    Blethrow, J
    Shimizu, E
    Tsien, JZ
    Schultz, PG
    Rose, MD
    Wood, JL
    Morgan, DO
    Shokat, KM
    [J]. NATURE, 2000, 407 (6802) : 395 - 401
  • [6] Design of allele-specific inhibitors to probe protein kinase signaling
    Bishop, AC
    Shah, K
    Liu, Y
    Witucki, L
    Kung, CY
    Shokat, KM
    [J]. CURRENT BIOLOGY, 1998, 8 (05) : 257 - 266
  • [7] Generation of monospecific nanomolar tyrosine kinase inhibitors via a chemical genetic approach
    Bishop, AC
    Kung, CY
    Shah, K
    Witucki, L
    Shokat, KM
    Liu, Y
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (04) : 627 - 631
  • [8] Braisted AC, 1997, METHOD ENZYMOL, V289, P298
  • [9] Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA
    Bruner, SD
    Norman, DPG
    Verdine, GL
    [J]. NATURE, 2000, 403 (6772) : 859 - 866
  • [10] Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors
    Chang, YT
    Gray, NS
    Rosania, GR
    Sutherlin, DP
    Kwon, S
    Norman, TC
    Sarohia, R
    Leost, M
    Meijer, L
    Schultz, PG
    [J]. CHEMISTRY & BIOLOGY, 1999, 6 (06): : 361 - 375