Functional analysis of the nuclear proteome of human A549 alveolar epithelial cells by HPLC-high resolution 2-D gel electrophoresis

被引:33
作者
Forbus, Jeffery
Spratt, Heidi
Wiktorowicz, John
Wu, Zheng
Boldogh, Istvan
Denner, Larry
Kurosky, Alexander
Brasier, Robert C.
Luxon, Bruce
Brasier, Allan R.
机构
[1] Univ Texas, Med Branch, Dept Med, Galveston, TX 77550 USA
[2] Univ Texas, Med Branch, NHLBI Proteom Ctr, Galveston, TX 77550 USA
[3] Univ Texas, Med Branch, Bioinformat Program, Galveston, TX 77550 USA
[4] Univ Texas, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77550 USA
[5] Univ Texas, Med Branch, Sealy Ctr Mol Sci, Galveston, TX 77550 USA
关键词
airway epithelial cell; 2-D gel electrophoresis; cell nucleus; protein networks;
D O I
10.1002/pmic.200500652
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The airway epithelial cell plays a central role in coordinating airway inflammatory responses, where significant changes in the proteome occur in response to infectious stimuli. To further understand the spectrum of proteins anal the biological processes they control, we have initially determined the nuclear proteome of human type II-like alveolar epithelial cells (A549) using a sequential method of organellar enrichment followed by HPLC prefractionation prior to 2-DE-based protein identification using MALDI-TOF MS. This approach yielded 719 high-confidence identifications, 433 mapping to unique gene identifiers. Expert classification showed that these proteins controlled chromatin remodeling, protein refolding, cytoskeletal structure, membrane function, metabolic processes, mitochondrial function, RNA binding, protein synthesis, signaling, and transcription factor activities. The proteins were mapped to gene ontology classifications, where metabolism and catalytic activity functions were significantly enriched, representing 43 and 32% of the protein set, respectively. Pathways analysis indicated a protein network affecting tumor necrosis factor-nuclear factor-kappa B signaling pathway interacting with intermediate cytoskeletal filaments. Forty-five proteins of unknown function were subjected to domain analysis and inferred to have additional nuclear functions controlling purine nucleotide metabolism and protein-protein interactions. This database represents the most comprehensive data set of mammalian nuclear proteins and will serve as a foundation for further discovery.
引用
收藏
页码:2656 / 2672
页数:17
相关论文
共 55 条
[31]   Regulation of a multigenic invasion programme by the transcription factor, AP-1: re-expression of a down-regulated gene, TSC-36, inhibits invasion [J].
Johnston, IMP ;
Spence, HJ ;
Winnie, JN ;
McGarry, L ;
Vass, JK ;
Meagher, L ;
Stapleton, G ;
Ozanne, BW .
ONCOGENE, 2000, 19 (47) :5348-5358
[32]   The beginning of the end:: IκB kinase (IKK) and NF-κB activation [J].
Karin, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (39) :27339-27342
[33]   Keratin 8 phosphorylation by p38 kinase regulates cellular keratin filament reorganization - Modulation by a keratin 1-like disease-causing mutation [J].
Ku, NO ;
Azhar, S ;
Omary, MB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) :10775-10782
[34]   Identification of proteins in slow continuous ultrafiltrate by reversed-phase chromatography and proteomics [J].
Lefler, DM ;
Pafford, RG ;
Black, NA ;
Raymond, JR ;
Arthur, JM .
JOURNAL OF PROTEOME RESEARCH, 2004, 3 (06) :1254-1260
[35]   Airway epithelium as an effector of inflammation: molecular regulation of secondary mediators [J].
Martin, LD ;
Rochelle, LG ;
Fischer, BM ;
Krunkosky, TM ;
Adler, KB .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (09) :2139-2146
[36]   Reversed-phase high-performance liquid chromatographic prefractionation of immunodepleted human serum proteins to enhance mass spectrometry identification of lower-abundant proteins [J].
Martosella, J ;
Zolotarjova, N ;
Liu, HB ;
Nicol, G ;
Boyes, BE .
JOURNAL OF PROTEOME RESEARCH, 2005, 4 (05) :1522-1537
[37]   InterPro, progress and status in 2005 [J].
Mulder, NJ ;
Apweiler, R ;
Attwood, TK ;
Bairoch, A ;
Bateman, A ;
Binns, D ;
Bradley, P ;
Bork, P ;
Bucher, P ;
Cerutti, L ;
Copley, R ;
Courcelle, E ;
Das, U ;
Durbin, R ;
Fleischmann, W ;
Gough, J ;
Haft, D ;
Harte, N ;
Hulo, N ;
Kahn, D ;
Kanapin, A ;
Krestyaninova, M ;
Lonsdale, D ;
Lopez, R ;
Letunic, I ;
Madera, M ;
Maslen, J ;
McDowall, J ;
Mitchell, A ;
Nikolskaya, AN ;
Orchard, S ;
Pagni, M ;
Pointing, CP ;
Quevillon, E ;
Selengut, J ;
Sigrist, CJA ;
Silventoinen, V ;
Studholme, DJ ;
Vaughan, R ;
Wu, CH .
NUCLEIC ACIDS RESEARCH, 2005, 33 :D201-D205
[38]   Epithelial cells as regulators of airway inflammation [J].
Polito, AJ ;
Proud, D .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1998, 102 (05) :714-718
[39]   Analysis of mitochondrial morphology and function with novel fixable fluorescent stains [J].
Poot, M ;
Zhang, YZ ;
Kramer, JA ;
Wells, KS ;
Jones, L ;
Hanzel, DK ;
Lugade, AG ;
Singer, VL ;
Haughland, RP .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1996, 44 (12) :1363-1372
[40]   PRO-INFLAMMATORY CYTOKINES AND ENVIRONMENTAL-STRESS CAUSE P38 MITOGEN-ACTIVATED PROTEIN-KINASE ACTIVATION BY DUAL PHOSPHORYLATION ON TYROSINE AND THREONINE [J].
RAINGEAUD, J ;
GUPTA, S ;
ROGERS, JS ;
DICKENS, M ;
HAN, JH ;
ULEVITCH, RJ ;
DAVIS, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) :7420-7426