Direct molecular Imaging of Lymnaea stagnalis nervous tissue at subcellular spatial resolution by mass spectrometry

被引:145
作者
Altelaar, AFM
van Minnen, J
Jiménez, CR
Heeren, RMA
Piersma, SR
机构
[1] FOM, Inst Atom & Mol Phys, NL-1098 SJ Amsterdam, Netherlands
[2] Free Univ Amsterdam, Fac Earth & Life Sci, Dept Mol & Cellular Neurobiol, NL-1081 HV Amsterdam, Netherlands
关键词
D O I
10.1021/ac048329g
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The imaging capabilities of time-of-flight secondary ion mass spectrometry (ToF-SIMS) and MALDI-MS sample preparation methods were combined. We used this method, named matrix-enhanced (ME) SIMS, for direct molecular imaging of nervous tissue at micrometer spatial resolution. Cryosections of the cerebral ganglia of the freshwater snail Lymnaea stagnalis were placed on indium-tin-oxide (ITO)-coated conductive glass slides and covered with a thin layer of 2,5-dihydroxybenzoic acid by electrospray deposition. High-resolution molecular ion maps of cholesterol and the neuropeptide APGWamide were constructed. APGWamide was predominantly localized in the cluster of neurons that regulate male copulation behavior of Lymnaea. ME-SIMS imaging allows direct molecule-specific imaging from tissue sections without labeling and opens a complementary mass window (<2500 Da) to MALDI imaging mass spectrometry at an order of magnitude higher spatial resolution (<3 mum).
引用
收藏
页码:735 / 741
页数:7
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