Literature DB >> 35094334

Green Chemistry Preservation and Extraction of Biospecimens for Multi-omic Analyses.

Andrey P Tikunov1, Jeremiah D Tipton1,2, Timothy J Garrett2, Sachi V Shinde1, Hong Jin Kim3, David A Gerber3, Laura E Herring4, Lee M Graves4, Jeffrey M Macdonald5.   

Abstract

The Environmental Protection Agency's definition of "Green Chemistry" is "the design of chemical products and processes that reduces or eliminates the use or generation of hazardous substances. Green chemistry applies across the life cycle of a chemical product, including its design, manufacture, use, and ultimate disposal." Conventional omic tissue extraction procedures use solvents that are toxic and carcinogenic, such as chloroform and methyl-tert-butyl ether for lipidomics, or caustic chaotropic solutions for genomics and transcriptomics, such as guanidine or urea. A common preservation solution for pathology is formaldehyde, which is a carcinogen. Use of acetonitrile as a universal biospecimen preservation and extraction solvent will reduce these hazardous wastes, because it is less toxic and more environmentally friendly than the conventional solvents used in biorepository and biospecimen research. A new extraction method never applied to multi-omic, system biology research, called cold-induced phase separation (CIPS), uses freezing point temperatures to induce a phase separation of acetonitrile-water mixtures. Also, the CO2 exposure during CIPS will acidify the water precipitating DNA out of aqueous phase. The resulting phase separation brings hydrophobic lipids to the top acetonitrile fraction that is easily decanted from the bottom aqueous fraction, especially when the water is frozen. This CIPS acetonitrile extract contains the lipidome (lipids), the bottom aqueous fraction is sampled to obtain the transcriptome (RNA) fraction, and the remaining water and pellet is extracted with 60% acetonitrile to isolate the metabolome (<1 kD polar molecules). Finally, steps 4 and 5 use a TRIzol™ liquid-liquid extraction SOP of the pellet to isolate the genome (DNA) and proteome (proteins). This chapter details the multi-omic sequential extraction SOP and potential problems associated with each of the 5 steps, with steps 2, 4, and 5 still requiring validation. The metabolomic and lipidomic extraction efficiencies using the CIPS SOP is compared to conventional solvent extraction SOPs and is analyzed by nuclear magnetic resonance (NMR) spectroscopy and liquid chromatography-mass spectrometry (LC-MS), respectively. Acetonitrile biospecimen preservation combined with the CIPS multi-omic extraction SOP is green chemistry technology that will eliminate the generation of the hazardous substances associated with biospecimen processing and permits separation and safe disposal of acetonitrile avoiding environmental contamination.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Acetonitrile; Biospecimen; CIPS; Green chemistry; Lipidomic; Metabolomics; Multi-Omics; Proteomics; QuEChERS; Switchable solvent

Mesh:

Substances:

Year:  2022        PMID: 35094334     DOI: 10.1007/978-1-0716-1811-0_17

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  58 in total

1.  The study of mammalian metabolism through NMR-based metabolomics.

Authors:  Reza Salek; Kian-Kai Cheng; Julian Griffin
Journal:  Methods Enzymol       Date:  2011       Impact factor: 1.600

Review 2.  Separation strategies for untargeted metabolomics.

Authors:  Gary J Patti
Journal:  J Sep Sci       Date:  2011-10-04       Impact factor: 3.645

3.  Strategy for choosing extraction procedures for NMR-based metabolomic analysis of mammalian cells.

Authors:  Estelle Martineau; Illa Tea; Gregory Loaëc; Patrick Giraudeau; Serge Akoka
Journal:  Anal Bioanal Chem       Date:  2011-08-13       Impact factor: 4.142

4.  Small molecule metabolite extraction strategy for improving LC/MS detection of cancer cell metabolome.

Authors:  Kathryn D Sheikh; Shefali Khanna; Stephen W Byers; Albert Fornace; Amrita K Cheema
Journal:  J Biomol Tech       Date:  2011-04

5.  Analysis of skeletal muscle metabolome: evaluation of extraction methods for targeted metabolite quantification using liquid chromatography tandem mass spectrometry.

Authors:  Rabih El Rammouz; Fabien Létisse; Stéphanie Durand; Jean-Charles Portais; Ziad Wadih Moussa; Xavier Fernandez
Journal:  Anal Biochem       Date:  2009-12-22       Impact factor: 3.365

6.  Comprehensive extraction method integrated with NMR metabolomics: a new bioactivity screening method for plants, adenosine A1 receptor binding compounds in Orthosiphon stamineus Benth.

Authors:  Nancy Dewi Yuliana; Alfi Khatib; Robert Verpoorte; Young Hae Choi
Journal:  Anal Chem       Date:  2011-08-08       Impact factor: 6.986

Review 7.  Mass spectrometry-based metabolomics, analysis of metabolite-protein interactions, and imaging.

Authors:  Do Yup Lee; Benjamin P Bowen; Trent R Northen
Journal:  Biotechniques       Date:  2010-08       Impact factor: 1.993

8.  Metabolite extraction from suspension-cultured mammalian cells for global metabolite profiling.

Authors:  Christopher A Sellick; Rasmus Hansen; Gill M Stephens; Royston Goodacre; Alan J Dickson
Journal:  Nat Protoc       Date:  2011-07-28       Impact factor: 13.491

9.  High-throughput tissue extraction protocol for NMR- and MS-based metabolomics.

Authors:  Huifeng Wu; Andrew D Southam; Adam Hines; Mark R Viant
Journal:  Anal Biochem       Date:  2007-10-09       Impact factor: 3.365

10.  Tissue fractionation by hydrostatic pressure cycling technology: the unified sample preparation technique for systems biology studies.

Authors:  Vera Gross; Greta Carlson; Ada T Kwan; Gary Smejkal; Emily Freeman; Alexander R Ivanov; Alexander Lazarev
Journal:  J Biomol Tech       Date:  2008-07
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