Cargando…

Self-assembling peptides imaged by correlated liquid cell transmission electron microscopy and MALDI-imaging mass spectrometry

We describe the observation of stimuli-induced peptide-based nanoscale assemblies by liquid cell transmission electron microscopy (LCTEM). LCTEM offers the opportunity to directly image nanoscale materials in liquid. Despite broad interest in characterizing biological phenomena, electron beam-induce...

Descripción completa

Detalles Bibliográficos
Autores principales: Touve, Mollie A., Carlini, Andrea S., Gianneschi, Nathan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811541/
https://www.ncbi.nlm.nih.gov/pubmed/31645558
http://dx.doi.org/10.1038/s41467-019-12660-1
_version_ 1783462484489797632
author Touve, Mollie A.
Carlini, Andrea S.
Gianneschi, Nathan C.
author_facet Touve, Mollie A.
Carlini, Andrea S.
Gianneschi, Nathan C.
author_sort Touve, Mollie A.
collection PubMed
description We describe the observation of stimuli-induced peptide-based nanoscale assemblies by liquid cell transmission electron microscopy (LCTEM). LCTEM offers the opportunity to directly image nanoscale materials in liquid. Despite broad interest in characterizing biological phenomena, electron beam-induced damage remains a significant problem. Concurrently, methods for verifying chemical structure during or following an LCTEM experiment have been few, with key examples limited to electron diffraction or elemental analysis of crystalline materials; this strategy is not translatable to biopolymers observed in nature. In this proof-of-concept study, oligomeric peptides are biologically or chemically stimulated within the liquid cell in a TEM to assemble into nanostructures. The resulting materials are analyzed by MALDI-imaging mass spectrometry (MALDI-IMS) to verify their identity. This approach confirms whether higher-order assemblies observed by LCTEM consist of intact peptides, verifying that observations made during the in situ experiment are because of those same peptides and not aberrant electron beam damage effects.
format Online
Article
Text
id pubmed-6811541
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-68115412019-10-25 Self-assembling peptides imaged by correlated liquid cell transmission electron microscopy and MALDI-imaging mass spectrometry Touve, Mollie A. Carlini, Andrea S. Gianneschi, Nathan C. Nat Commun Article We describe the observation of stimuli-induced peptide-based nanoscale assemblies by liquid cell transmission electron microscopy (LCTEM). LCTEM offers the opportunity to directly image nanoscale materials in liquid. Despite broad interest in characterizing biological phenomena, electron beam-induced damage remains a significant problem. Concurrently, methods for verifying chemical structure during or following an LCTEM experiment have been few, with key examples limited to electron diffraction or elemental analysis of crystalline materials; this strategy is not translatable to biopolymers observed in nature. In this proof-of-concept study, oligomeric peptides are biologically or chemically stimulated within the liquid cell in a TEM to assemble into nanostructures. The resulting materials are analyzed by MALDI-imaging mass spectrometry (MALDI-IMS) to verify their identity. This approach confirms whether higher-order assemblies observed by LCTEM consist of intact peptides, verifying that observations made during the in situ experiment are because of those same peptides and not aberrant electron beam damage effects. Nature Publishing Group UK 2019-10-23 /pmc/articles/PMC6811541/ /pubmed/31645558 http://dx.doi.org/10.1038/s41467-019-12660-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Touve, Mollie A.
Carlini, Andrea S.
Gianneschi, Nathan C.
Self-assembling peptides imaged by correlated liquid cell transmission electron microscopy and MALDI-imaging mass spectrometry
title Self-assembling peptides imaged by correlated liquid cell transmission electron microscopy and MALDI-imaging mass spectrometry
title_full Self-assembling peptides imaged by correlated liquid cell transmission electron microscopy and MALDI-imaging mass spectrometry
title_fullStr Self-assembling peptides imaged by correlated liquid cell transmission electron microscopy and MALDI-imaging mass spectrometry
title_full_unstemmed Self-assembling peptides imaged by correlated liquid cell transmission electron microscopy and MALDI-imaging mass spectrometry
title_short Self-assembling peptides imaged by correlated liquid cell transmission electron microscopy and MALDI-imaging mass spectrometry
title_sort self-assembling peptides imaged by correlated liquid cell transmission electron microscopy and maldi-imaging mass spectrometry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811541/
https://www.ncbi.nlm.nih.gov/pubmed/31645558
http://dx.doi.org/10.1038/s41467-019-12660-1
work_keys_str_mv AT touvemolliea selfassemblingpeptidesimagedbycorrelatedliquidcelltransmissionelectronmicroscopyandmaldiimagingmassspectrometry
AT carliniandreas selfassemblingpeptidesimagedbycorrelatedliquidcelltransmissionelectronmicroscopyandmaldiimagingmassspectrometry
AT gianneschinathanc selfassemblingpeptidesimagedbycorrelatedliquidcelltransmissionelectronmicroscopyandmaldiimagingmassspectrometry