Alzheimer's disease:: Correlation of the suppression of β-amyloid peptide secretion from cultured cells with inhibition of the chymotrypsin-like activity of the proteasome

被引:31
作者
Christie, G
Markwell, RE
Gray, CW
Smith, L
Godfrey, F
Mansfield, F
Wadsworth, H
King, R
McLaughlin, M
Cooper, DG
Ward, RV
Howlett, DR
Hartmann, T
Lichtenthaler, SF
Beyreuther, K
Underwood, J
Gribble, SK
Cappai, R
Masters, CL
Tamaoka, A
Gardner, RL
Rivett, AJ
Karran, EH
Allsop, D
机构
[1] SmithKline Beecham Pharmaceut, Harlow CM19 5AW, Essex, England
[2] Univ Bristol, Sch Med Sci, Dept Biochem, Bristol BS8 1TD, Avon, England
[3] Heidelberg Univ, Ctr Mol Biol, D-6900 Heidelberg, Germany
[4] Univ Melbourne, Dept Pathol, Parkville, Vic 3052, Australia
[5] Univ Tsukuba, Inst Clin Med, Tsukuba, Ibaraki 305, Japan
关键词
Alzheimer's disease; amyloid; beta-amyloid peptide; proteasome; inhibitor;
D O I
10.1046/j.1471-4159.1999.0730195.x
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
Peptide aldehyde inhibitors of the chymotrypsin-like activity of the proteasome (CLIP) such as N-acetyl-Leu-Leu-Nle-H (or ALLN) have been shown previously to inhibit the secretion of beta-amyloid peptide (A beta) from cells. To evaluate more fully the role of the proteasome in this process, we have tested the effects on A beta formation of a much wider range of peptide-based inhibitors of CLIP than published previously. The inhibitors tested included several peptide boronates, some of which proved to be the most potent peptide-based inhibitors of beta-amyloid production reported so far. We found that the ability of the peptide aldehyde and boronate inhibitors to suppress A beta formation from cells correlated extremely well with their potency as CLIP inhibitors. Thus, we conclude that the proteasome may be involved either directly or indirectly in A beta formation.
引用
收藏
页码:195 / 204
页数:10
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