MALDI-ion mobility-TOFMS imaging of lipids in rat brain tissue

被引:185
作者
Jackson, Shelley N.
Ugarov, Michael
Egan, Thomas
Post, Jeremy D.
Langlais, Denis
Schultz, J. Albert
Woods, Amina S.
机构
[1] NIDA, IRP, NIH, Baltimore, MD 21224 USA
[2] Lonwerks Inc, Houston, TX USA
来源
JOURNAL OF MASS SPECTROMETRY | 2007年 / 42卷 / 08期
关键词
ion mobility MS; lipid imaging; brain tissue; phosphatidylcholines; cerebrosides;
D O I
10.1002/jms.1245
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
While maintaining anatomical integrity, matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS) has allowed researchers to directly probe tissue, map the distribution of analytes and elucidate molecular structure with minimal preparation. MALDI-ion mobility (IM)-orthogonal time-of-flight mass spectrometry (oTOFMS) provides an advantage by initially separating different classes of biomolecules such as lipids, peptides, and nucleotides by their IM drift times prior to mass analysis. In the present work the distribution of phosphatidlycholine and cerebroside species was mapped from 16 mu m thick coronal rat brain sections using MALDI-IM-oTOFMS. Furthermore, the use of gold nanoparticles as a matrix enables detection of cerebrosides, which although highly concentrated in brain tissue, are not easily observed as positive ions because of intense signals from lipids such as phosphatidlycholines and sphingomyelins. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:1093 / 1098
页数:6
相关论文
共 33 条
[1]  
Agranoff Bernard W., 1999, P47
[2]   Distribution of cholesterol and galactosylceramide in rat cerebellar white matter [J].
Boerner, Katrin ;
Nygren, Hakan ;
Hagenhoff, Birgit ;
Malmberg, Per ;
Tallarek, Elke ;
Mansson, Jan-Eric .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2006, 1761 (03) :335-344
[3]   Tissue profiling by mass spectrometry - A review of methodology and applications [J].
Caldwell, RL ;
Caprioli, RM .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (04) :394-401
[4]   Imaging mass spectrometry: Principles and potentials [J].
Chaurand, P ;
Schwartz, SA ;
Reyzer, ML ;
Caprioli, RA .
TOXICOLOGIC PATHOLOGY, 2005, 33 (01) :92-101
[5]   New developments in profiling and imaging of proteins from tissue sections by MALDI mass spectrometry [J].
Chaurand, Pierre ;
Norris, Jeremy L. ;
Cornett, D. Shannon ;
Mobley, James A. ;
Caprioli, Richard M. .
JOURNAL OF PROTEOME RESEARCH, 2006, 5 (11) :2889-2900
[6]  
Fournier I, 2003, NEUROENDOCRINOL LETT, V24, P9
[7]   Imaging of small molecules in tissue sections with a new intermediate-pressure MALDI linear ion trap mass spectrometer [J].
Garrett, Timothy J. ;
Prieto-Conaway, Maria C. ;
Kovtoun, Viatcheslav ;
Bui, Huy ;
Izgarian, Nick ;
Stafford, George ;
Yost, Richard A. .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2007, 260 (2-3) :166-176
[8]   Coupling high-pressure MALDI with ion mobility/orthogonal time-of flight mass spectrometry [J].
Gillig, KJ ;
Ruotolo, B ;
Stone, EG ;
Russell, DH ;
Fuhrer, K ;
Gonin, M ;
Schultz, AJ .
ANALYTICAL CHEMISTRY, 2000, 72 (17) :3965-3971
[9]   Identification of proteins directly from tissue:: in situ tryptic digestions coupled with imaging mass spectrometry [J].
Groseclose, M. Reid ;
Andersson, Malin ;
Hardesty, William M. ;
Caprioli, Richard M. .
JOURNAL OF MASS SPECTROMETRY, 2007, 42 (02) :254-262
[10]   Characterization and direct quantitation of cerebroside molecular species from lipid extracts by shotgun lipidomics [J].
Han, XL ;
Cheng, H .
JOURNAL OF LIPID RESEARCH, 2005, 46 (01) :163-175