| Literature DB >> 32519547 |
Andreas Dannhorn1,2, Emine Kazanc1, Stephanie Ling2, Chelsea Nikula3, Evdoxia Karali4, Maria Paola Serra2, Jean-Luc Vorng3, Paolo Inglese1, Gareth Maglennon5, Gregory Hamm2, John Swales2, Nicole Strittmatter2, Simon T Barry6, Owen J Sansom7, George Poulogiannis4, Josephine Bunch3, Richard Ja Goodwin2, Zoltan Takats1.
Abstract
A new tissue sample embedding and processing method is presented that provides downstream compatibility with numerous different histological, molecular biology, and analytical techniques. The methodology is based on the low temperature embedding of fresh frozen specimens into a hydrogel matrix composed of hydroxypropyl methylcellulose (HPMC) and polyvinylpyrrolidone (PVP) and sectioning using a cryomicrotome. The hydrogel was expected not to interfere with standard tissue characterization methods, histologically or analytically. We assessed the compatibility of this protocol with various mass spectrometric imaging methods including matrix-assisted laser desorption ionization (MALDI), desorption electrospray ionization (DESI) and secondary ion mass spectrometry (SIMS). We also demonstrated the suitability of the universal protocol for extraction based molecular biology techniques such as rt-PCR. The integration of multiple analytical modalities through this universal sample preparation protocol offers the ability to study tissues at a systems biology level and directly linking results to tissue morphology and cellular phenotype.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32519547 DOI: 10.1021/acs.analchem.0c00826
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986