Detection and quantitation of cellularly derived amyloid β peptides by immunoprecipitation-HPLC-MS

被引:37
作者
Clarke, NJ
Tomlinson, AJ
Ohyagi, Y
Younkin, S
Naylor, S
机构
[1] Mayo Clin Jacksonville, Dept Pharmacol, Jacksonville, FL 32224 USA
[2] Mayo Clin & Mayo Fdn, Dept Biochem & Mol Biol, Biomed Mass Spect Facil, Rochester, MN 55905 USA
[3] Iizuka Hosp, Dept Neurol, Iizuka, Fukuoka 820, Japan
[4] Mayo Clin & Mayo Fdn, Dept Pharmacol, Rochester, MN 55905 USA
[5] Mayo Clin & Mayo Fdn, Clin Pharmacol Unit, Rochester, MN 55905 USA
关键词
Alzheimer's disease; amyloid beta; HPLC; immunoprecipitation; mass spectrometry;
D O I
10.1016/S0014-5793(98)00706-6
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
A quantitative method for detection of amyloid beta peptides using immunoprecipitation-HPLC-mass spectrometry (IP-LC-MS) is described, Comparison of IP-LC-MS with sandwich ELISA revealed comparable results in the analysis of A beta 1-40 and A beta 1-42 derived from fetal guinea pig cell media and cell lysates. The use of IP-LC-MS not only allows a quantitative method for A beta 1-40 and A beta 1-42 peptides present in Alzheimer's disease (AD), but allows detection of other A beta peptide species that may also play a role in the onset of AD in humans. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:419 / 423
页数:5
相关论文
共 19 条
  • [1] Alzheimer transgenic mouse models come of age
    Duff, K
    [J]. TRENDS IN NEUROSCIENCES, 1997, 20 (07) : 279 - 280
  • [2] AMYLOID-BETA PROTEIN (A-BETA) IN ALZHEIMERS-DISEASE BRAIN - BIOCHEMICAL AND IMMUNOCYTOCHEMICAL ANALYSIS WITH ANTIBODIES SPECIFIC FOR FORMS ENDING AT A-BETA-40 OR A-BETA-42(43)
    GRAVINA, SA
    HO, LB
    ECKMAN, CB
    LONG, KE
    OTVOS, L
    YOUNKIN, LH
    SUZUKI, N
    YOUNKIN, SG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) : 7013 - 7016
  • [3] HILBICH C, 1993, J BIOL CHEM, V268, P26571
  • [4] Correlative memory deficits, A beta elevation, and amyloid plaques in transgenic mice
    Hsiao, K
    Chapman, P
    Nilsen, S
    Eckman, C
    Harigaya, Y
    Younkin, S
    Yang, FS
    Cole, G
    [J]. SCIENCE, 1996, 274 (5284) : 99 - 102
  • [5] SEEDING ONE-DIMENSIONAL CRYSTALLIZATION OF AMYLOID - A PATHOGENIC MECHANISM IN ALZHEIMERS-DISEASE AND SCRAPIE
    JARRETT, JT
    LANSBURY, PT
    [J]. CELL, 1993, 73 (06) : 1055 - 1058
  • [6] Katzman Robert, 1994, P105
  • [7] THE HIGHLY EFFICIENT PRODUCTION OF FULL-LENGTH AND MUTANT RAT-BRAIN CALCIUM-BINDING PROTEINS (CALBINDINS-D-28K) IN A BACTERIAL EXPRESSION SYSTEM
    KUMAR, R
    HUNZIKER, W
    GROSS, M
    NAYLOR, S
    LONDOWSKI, JM
    SCHAEFER, J
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1994, 308 (01) : 311 - 317
  • [8] Identifying sites of protein modification by using matrix-assisted laser desorption ionization-time-of-flight mass spectrometry and on-line membrane preconcentration capillary electrophoresis tandem mass spectrometry
    Kurian, E
    Prendergast, FG
    Tomlinson, AJ
    Holmes, MW
    Naylor, S
    [J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1997, 8 (01) : 8 - 14
  • [9] PEPTIDE COMPOSITIONS OF THE CEREBROVASCULAR AND SENILE PLAQUE CORE AMYLOID DEPOSITS OF ALZHEIMERS-DISEASE
    MILLER, DL
    PAPAYANNOPOULOS, IA
    STYLES, J
    BOBIN, SA
    LIN, YY
    BIEMANN, K
    IQBAL, K
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 301 (01) : 41 - 52
  • [10] MORI H, 1992, J BIOL CHEM, V267, P17082