A screening UHPLC-MS/MS method for the analysis of amyloid peptides in cerebrospinal fluid of preclinical species

被引:20
作者
Dillen, Lieve [1 ]
Cools, Willy [1 ]
Vereyken, Liesbeth [1 ]
Timmerman, Philip [1 ]
机构
[1] Janssen Res & Dev, Div Janssen Pharmaceut NV, Bioanal Dept, B-2340 Beerse, Belgium
关键词
QUANTITATIVE-ANALYSIS; ALZHEIMERS-DISEASE; ABSOLUTE QUANTIFICATION; GAMMA-SECRETASE; BETA PEPTIDES; VALIDATION; PLASMA; IMMUNOPRECIPITATION; RECOMMENDATIONS; CHROMATOGRAPHY;
D O I
10.4155/BIO.10.163
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Amyloid peptides are established biomarkers for Alzheimer's disease but their analysis presents major challenges. Results: In this article, we describe the use of ultra high-performance LC and API4000 triple quadrupole instrumentation for the quantification of amyloid peptides (A beta(1-38) and A beta(1-42)) in cerebrospinal fluid (CSF), using electrospray ionization with negative ion multiple reaction monitoring transitions. Sample preparation was simplified by the addition of acetonitrile and ammonium hydroxide. Although excellent sensitivity and precision was demonstrated, we observed differences in matrix suppression effects when using artificial CSF versus canine CSF for calibration curves and quality control samples. Conclusion: A case study shows that the method can be used to determine the relative levels of two key peptides (A beta(1-38) and A beta(1-42)) compared with their predose values (a screening assay) in support of preclinical studies.
引用
收藏
页码:45 / 55
页数:11
相关论文
共 30 条
[1]   Quantification of small therapeutic proteins in plasma by liquid chromatography - Tandem mass spectrometry: Application to an elastase inhibitor EPI-hNE4 [J].
Becher, F ;
Pruvost, A ;
Clement, G ;
Tabet, JC ;
Ezan, E .
ANALYTICAL CHEMISTRY, 2006, 78 (07) :2306-2313
[2]   CSF markers for incipient Alzheimer's disease [J].
Blennow, K ;
Hampel, H .
LANCET NEUROLOGY, 2003, 2 (10) :605-613
[3]  
Cirrito JR, 2003, J NEUROSCI, V23, P8844
[4]   Analysis of in vivo-derived amyloid-β polypeptides by on-line two-dimensional chromatography-mass spectrometry [J].
Clarke, NJ ;
Crow, FW ;
Younkin, S ;
Naylor, S .
ANALYTICAL BIOCHEMISTRY, 2001, 298 (01) :32-39
[5]   Recommendations for the bioanalytical method validation of ligand-binding assays to support pharmacokinetic assessments of macromolecules [J].
DeSilva, B ;
Smith, W ;
Weiner, R ;
Kelley, M ;
Smolec, JM ;
Lee, B ;
Khan, M ;
Tacey, R ;
Hill, H ;
Celniker, A .
PHARMACEUTICAL RESEARCH, 2003, 20 (11) :1885-1900
[6]  
DU C, 2005, BIOMOL TECHN, V16, P356
[7]   Inhibition of γ-secretase as a therapeutic intervention for Alzheimer's disease -: Prospects, limitations and strategies [J].
Evin, Genevieve ;
Sernee, Marijke Fleur ;
Masters, Colin L. .
CNS DRUGS, 2006, 20 (05) :351-372
[8]   Inverse relation between in vivo amyloid imaging load and cerebrospinal fluid Aβ42 in humans [J].
Fagan, AM ;
Mintun, MA ;
Mach, RH ;
Lee, SY ;
Dence, CS ;
Shah, AR ;
LaRossa, GN ;
Spinner, ML ;
Klunk, WE ;
Mathis, CA ;
DeKosky, ST ;
Morris, JC ;
Holtzman, DM .
ANNALS OF NEUROLOGY, 2006, 59 (03) :512-519
[9]  
Gelfanova Valentina, 2007, Briefings in Functional Genomics & Proteomics, V6, P149, DOI 10.1093/bfgp/elm010
[10]   Quantitative analysis of complex protein mixtures using isotope-coded affinity tags [J].
Gygi, SP ;
Rist, B ;
Gerber, SA ;
Turecek, F ;
Gelb, MH ;
Aebersold, R .
NATURE BIOTECHNOLOGY, 1999, 17 (10) :994-999