MALDI imaging mass spectrometry for direct tissue analysis:: a new frontier for molecular histology

被引:235
作者
Walch, Axel [1 ]
Rauser, Sandra [1 ]
Deininger, Soeren-Oliver [2 ]
Hoefler, Heinz [1 ,3 ]
机构
[1] Deutsch Forschungszentrum Gesundheit & Umwelt Gmb, Helmholtz Zentrum Munchen, Inst Pathol, D-85764 Neuherberg, Germany
[2] Bruker Daltonik GmbH, Bremen, Germany
[3] Tech Univ Munich, Inst Pathol, Munich, Germany
关键词
MALDI imaging mass spectrometry; tissue; in situ-proteomics; pathology;
D O I
10.1007/s00418-008-0469-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Matrix-assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) is a powerful tool for investigating the distribution of proteins and small molecules within biological systems through the in situ analysis of tissue sections. MALDI-IMS can determine the distribution of hundreds of unknown compounds in a single measurement and enables the acquisition of cellular expression profiles while maintaining the cellular and molecular integrity. In recent years, a great many advances in the practice of imaging mass spectrometry have taken place, making the technique more sensitive, robust, and ultimately useful. In this review, we focus on the current state of the art of MALDI-IMS, describe basic technological developments for MALDI-IMS of animal and human tissues, and discuss some recent applications in basic research and in clinical settings.
引用
收藏
页码:421 / 434
页数:14
相关论文
共 91 条
[1]   Mass spectrometry in proteomics [J].
Aebersold, R ;
Goodlett, DR .
CHEMICAL REVIEWS, 2001, 101 (02) :269-295
[2]   Automated acoustic matrix deposition for MALDI sample preparation [J].
Aerni, HR ;
Cornett, DS ;
Caprioli, RM .
ANALYTICAL CHEMISTRY, 2006, 78 (03) :827-834
[3]   Imaging mass spectrometry at cellular length scales [J].
Altelaar, A. F. Maarten ;
Luxembourg, Stefan L. ;
McDonnell, Liam A. ;
Piersma, Sander R. ;
Heeren, Ron M. A. .
NATURE PROTOCOLS, 2007, 2 (05) :1185-1196
[4]   Gold-enhanced biomolecular surface imaging of cells and tissue by SIMS and MALDI mass spectrometry [J].
Altelaar, AFM ;
Klinkert, I ;
Jalink, K ;
de Lange, RPJ ;
Adan, RAH ;
Heeren, RMA ;
Piersma, SR .
ANALYTICAL CHEMISTRY, 2006, 78 (03) :734-742
[5]   Direct molecular Imaging of Lymnaea stagnalis nervous tissue at subcellular spatial resolution by mass spectrometry [J].
Altelaar, AFM ;
van Minnen, J ;
Jiménez, CR ;
Heeren, RMA ;
Piersma, SR .
ANALYTICAL CHEMISTRY, 2005, 77 (03) :735-741
[6]   Laser capture microdissection MALDI for direct analysis of archival tissue [J].
Bhattacharya, SH ;
Gal, AA ;
Murray, KK .
JOURNAL OF PROTEOME RESEARCH, 2003, 2 (01) :95-98
[7]   Bradykinin-related peptides from Phyllomedusa hypochondrialis [J].
Brand, G. D. ;
Krause, F. C. ;
Silva, L. P. ;
Leite, J. R. S. A. ;
Melo, J. A. T. ;
Prates, M. V. ;
Pesquero, J. B. ;
Santos, E. L. ;
Nakaie, C. R. ;
Costa-Neto, C. M. ;
Bloch, C., Jr. .
PEPTIDES, 2006, 27 (09) :2137-2146
[8]  
BURNUM KE, 2008, ENDOCRINOLOGY 0410
[9]   Tissue profiling by mass spectrometry - A review of methodology and applications [J].
Caldwell, RL ;
Caprioli, RM .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (04) :394-401
[10]   Deciphering protein molecular signatures in cancer tissues to aid in diagnosis, prognosis, and therapy [J].
Caprioli, RM .
CANCER RESEARCH, 2005, 65 (23) :10642-10645