Cargando…

Single-cell omics analyses with single molecular detection: challenges and perspectives

The ultimate goal of single-cell analyses is to obtain the biomolecular content for each cell in unicellular and multicellular organisms at different points of their life cycle under variable environmental conditions. These require an assessment of: a) the total number of cells, b) the total number...

Descripción completa

Detalles Bibliográficos
Autor principal: Misevic, Gradimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383168/
https://www.ncbi.nlm.nih.gov/pubmed/34253696
http://dx.doi.org/10.7555/JBR.35.20210026
_version_ 1783741684853506048
author Misevic, Gradimir
author_facet Misevic, Gradimir
author_sort Misevic, Gradimir
collection PubMed
description The ultimate goal of single-cell analyses is to obtain the biomolecular content for each cell in unicellular and multicellular organisms at different points of their life cycle under variable environmental conditions. These require an assessment of: a) the total number of cells, b) the total number of cell types, and c) the complete and quantitative single molecular detection and identification for all classes of biopolymers, and organic and inorganic compounds, in each individual cell. For proteins, glycans, lipids, and metabolites, whose sequences cannot be amplified by copying as in the case of nucleic acids, the detection limit by mass spectrometry is about 10(5) molecules. Therefore, proteomic, glycomic, lipidomic, and metabolomic analyses do not yet permit the assembly of the complete single-cell omes. The construction of novel nanoelectrophoretic arrays and nano in microarrays on a single 1-cm-diameter chip has shown proof of concept for a high throughput platform for parallel processing of thousands of individual cells. Combined with dynamic secondary ion mass spectrometry, with 3D scanning capability and lateral resolution of 50 nm, the sensitivity of single molecular quantification and identification for all classes of biomolecules could be reached. Further development and routine application of such technological and instrumentation solution would allow assembly of complete omes with a quantitative assessment of structural and functional cellular diversity at the molecular level.
format Online
Article
Text
id pubmed-8383168
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Editorial Department of Journal of Biomedical Research
record_format MEDLINE/PubMed
spelling pubmed-83831682021-09-03 Single-cell omics analyses with single molecular detection: challenges and perspectives Misevic, Gradimir J Biomed Res Review Article The ultimate goal of single-cell analyses is to obtain the biomolecular content for each cell in unicellular and multicellular organisms at different points of their life cycle under variable environmental conditions. These require an assessment of: a) the total number of cells, b) the total number of cell types, and c) the complete and quantitative single molecular detection and identification for all classes of biopolymers, and organic and inorganic compounds, in each individual cell. For proteins, glycans, lipids, and metabolites, whose sequences cannot be amplified by copying as in the case of nucleic acids, the detection limit by mass spectrometry is about 10(5) molecules. Therefore, proteomic, glycomic, lipidomic, and metabolomic analyses do not yet permit the assembly of the complete single-cell omes. The construction of novel nanoelectrophoretic arrays and nano in microarrays on a single 1-cm-diameter chip has shown proof of concept for a high throughput platform for parallel processing of thousands of individual cells. Combined with dynamic secondary ion mass spectrometry, with 3D scanning capability and lateral resolution of 50 nm, the sensitivity of single molecular quantification and identification for all classes of biomolecules could be reached. Further development and routine application of such technological and instrumentation solution would allow assembly of complete omes with a quantitative assessment of structural and functional cellular diversity at the molecular level. Editorial Department of Journal of Biomedical Research 2021-07 2021-04-30 /pmc/articles/PMC8383168/ /pubmed/34253696 http://dx.doi.org/10.7555/JBR.35.20210026 Text en Copyright and License information: Journal of Biomedical Research, CAS Springer-Verlag Berlin Heidelberg 2021 https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Review Article
Misevic, Gradimir
Single-cell omics analyses with single molecular detection: challenges and perspectives
title Single-cell omics analyses with single molecular detection: challenges and perspectives
title_full Single-cell omics analyses with single molecular detection: challenges and perspectives
title_fullStr Single-cell omics analyses with single molecular detection: challenges and perspectives
title_full_unstemmed Single-cell omics analyses with single molecular detection: challenges and perspectives
title_short Single-cell omics analyses with single molecular detection: challenges and perspectives
title_sort single-cell omics analyses with single molecular detection: challenges and perspectives
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383168/
https://www.ncbi.nlm.nih.gov/pubmed/34253696
http://dx.doi.org/10.7555/JBR.35.20210026
work_keys_str_mv AT misevicgradimir singlecellomicsanalyseswithsinglemoleculardetectionchallengesandperspectives