Proteomics-driven progress in neurodegeneration research

被引:52
作者
Fountoulakis, Michael [1 ]
Kossida, Sophia [1 ]
机构
[1] Acad Athens, Div Biotechnol, Fdn Biomed Res, GR-11527 Athens, Greece
关键词
Alzheimer's disease; brain; cerebrospinal fluid; Down syndrome; neuroproteomics;
D O I
10.1002/elps.200500738
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Proteomics technologies have been widely used in the investigation of neurodegenerative and psychiatric disorders, and in particular in the detection of differences between healthy individuals and patients suffering from such diseases. Thus, brain and cerebrospinal fluid (CSF) samples from patients with Alzheimer's disease, Down syndrome, Pick's disease, Parkinson's disease, schizophrenia, and other disorders as well as brain and CSF from animals serving as models of neurological disorders have been analyzed by proteomics. 2-DE followed by MALDI-TOF-MS has been mainly applied as this proteomics approach provides the possibility of convenient quantification of protein levels and detection of post-translational modifications. About 330 unique proteins with deranged levels and modifications have been detected by proteomics approaches to be related to neurodegeneration and psychiatric disorders. They are mainly involved in metabolism pathways, cytoskeleton formation, signal transduction, guidance, detoxification, transport, and conformational changes. In this article, we provide a summary of the major contributions of proteomics technologies in the study of neurodegenerative and psychiatric diseases, in particular, in the detection of changes in protein levels and modifications related to these disorders.
引用
收藏
页码:1556 / 1573
页数:18
相关论文
共 208 条
[1]
Oxidative modification of creatine kinase BB in Alzheimer's disease brain [J].
Aksenov, M ;
Aksenova, M ;
Butterfield, DA ;
Markesbery, WR .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (06) :2520-2527
[2]
ApoC-I and ApoC-III as potential plasmatic markers to distinguish between ischemic and hemorrhagic stroke [J].
Allard, L ;
Lescuyer, P ;
Burgess, J ;
Leung, KY ;
Ward, M ;
Walter, N ;
Burkhard, PR ;
Corthals, G ;
Hochstrasser, DF ;
Sanchez, JC .
PROTEOMICS, 2004, 4 (08) :2242-2251
[3]
Proteomic identification of brainstem cytosolic proteins in a neuropathic pain model [J].
Alzate, O ;
Hussain, SRA ;
Goett, VM ;
Tewari, AK ;
Madiai, F ;
Stephens, RL ;
Hackshaw, KV .
MOLECULAR BRAIN RESEARCH, 2004, 128 (02) :193-200
[4]
10 years of genomics, chromosome 21, and Down syndrome [J].
Antonarakis, SE .
GENOMICS, 1998, 51 (01) :1-16
[5]
Bajo M, 2002, PROTEOMICS, V2, P1539, DOI 10.1002/1615-9861(200211)2:11<1539::AID-PROT1539>3.0.CO
[6]
2-C
[7]
Neurofilament proteins NF-L, NF-M and NF-H in brain of patients with Down syndrome and Alzheimer's disease [J].
Bajo, M ;
Yoo, BC ;
Cairns, N ;
Gratzer, M ;
Lubec, G .
AMINO ACIDS, 2001, 21 (03) :293-301
[8]
Balcz B, 2001, J NEURAL TRANSM-SUPP, P193
[9]
Proteomics: new perspectives, new biomedical opportunities [J].
Banks, RE ;
Dunn, MJ ;
Hochstrasser, DF ;
Sanchez, JC ;
Blackstock, W ;
Pappin, DJ ;
Selby, PJ .
LANCET, 2000, 356 (9243) :1749-1756
[10]
Emerging principles of altered neural circuitry in schizophrenia [J].
Benes, FM .
BRAIN RESEARCH REVIEWS, 2000, 31 (2-3) :251-269