PMID- 29602282 OWN - NLM STAT- MEDLINE DCOM- 20190225 LR - 20190225 IS - 1559-4106 (Electronic) IS - 1559-4106 (Linking) VI - 13 IP - 3 DP - 2018 Mar 30 TI - Comparison between thaw-mounting and use of conductive tape for sample preparation in ToF-SIMS imaging of lipids in Drosophila microRNA-14 model. PG - 03B414 LID - 10.1116/1.5019597 [doi] AB - Time-of-flight secondary ion mass spectrometry (ToF-SIMS) imaging elucidates molecular distributions in tissue sections, providing useful information about the metabolic pathways linked to diseases. However, delocalization of the analytes and inadequate tissue adherence during sample preparation are among some of the unfortunate phenomena associated with this technique due to their role in the reduction of the quality, reliability, and spatial resolution of the ToF-SIMS images. For these reasons, ToF-SIMS imaging requires a more rigorous sample preparation method in order to preserve the natural state of the tissues. The traditional thaw-mounting method is particularly vulnerable to altered distributions of the analytes due to thermal effects, as well as to tissue shrinkage. In the present study, the authors made comparisons of different tissue mounting methods, including the thaw-mounting method. The authors used conductive tape as the tissue-mounting material on the substrate because it does not require heat from the finger for the tissue section to adhere to the substrate and can reduce charge accumulation during data acquisition. With the conductive-tape sampling method, they were able to acquire reproducible tissue sections and high-quality images without redistribution of the molecules. Also, the authors were successful in preserving the natural states and chemical distributions of the different components of fat metabolites such as diacylglycerol and fatty acids by using the tape-supported sampling in microRNA-14 (miR-14) deleted Drosophila models. The method highlighted here shows an improvement in the accuracy of mass spectrometric imaging of tissue samples. FAU - Le, Minh Uyen Thi AU - Le MUT AD - Department of Nano Science, University of Science and Technology (UST), Daejeon 34113, South Korea and Center for Nano-Bio Measurement, Korea Research Institute of Standards and Science (KRISS), Daejeon 34113, South Korea. FAU - Son, Jin Gyeong AU - Son JG AD - Center for Nano-Bio Measurement, Korea Research Institute of Standards and Science (KRISS), Daejeon 34113, South Korea. FAU - Shon, Hyun Kyoung AU - Shon HK AD - Center for Nano-Bio Measurement, Korea Research Institute of Standards and Science (KRISS), Daejeon 34113, South Korea. FAU - Park, Jeong Hyang AU - Park JH AD - Department of Brain and Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, South Korea. FAU - Lee, Sung Bae AU - Lee SB AD - Department of Brain and Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, South Korea. FAU - Lee, Tae Geol AU - Lee TG AD - Department of Nano Science, University of Science and Technology (UST), Daejeon 34113, South Korea and Center for Nano-Bio Measurement, Korea Research Institute of Standards and Science (KRISS), Daejeon 34113, South Korea. LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20180330 PL - United States TA - Biointerphases JT - Biointerphases JID - 101275679 RN - 0 (Lipids) RN - 0 (MIRN14 microRNA, Drosophila) RN - 0 (MicroRNAs) SB - IM MH - Animals MH - Drosophila/*chemistry/genetics MH - Gene Deletion MH - Histocytological Preparation Techniques/*methods MH - Image Processing, Computer-Assisted/*methods MH - Lipids/*analysis MH - MicroRNAs/genetics MH - Reproducibility of Results MH - Spectrometry, Mass, Secondary Ion/*methods EDAT- 2018/04/01 06:00 MHDA- 2019/02/26 06:00 CRDT- 2018/04/01 06:00 PHST- 2018/04/01 06:00 [entrez] PHST- 2018/04/01 06:00 [pubmed] PHST- 2019/02/26 06:00 [medline] AID - 10.1116/1.5019597 [doi] PST - epublish SO - Biointerphases. 2018 Mar 30;13(3):03B414. doi: 10.1116/1.5019597.