Self-Assembly of Pseudo-Isocyanine Chloride as a Sensor for Macromolecular Crowding In Vitro and In Vivo.


Journal

Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783

Informations de publication

Date de publication:
02 Jun 2020
Historique:
received: 09 01 2020
revised: 20 02 2020
pubmed: 11 3 2020
medline: 5 9 2020
entrez: 11 3 2020
Statut: ppublish

Résumé

Pseudo-isocyanine chloride (PIC) is a cationic dyestuff that exhibits self-assembly in aqueous solution, promoted either by increasing the PIC concentration or by decreasing the temperature. PIC-aggregates exhibit a characteristic and sharp absorption band as well as a fluorescence band at a wavelength of 573 nm making PIC an interesting candidate to analyze the self-assembly process in various environments. The present work developed PIC-based, synthetic model systems, suitable to investigate how macromolecular crowding influences self-assembly processes. Four synthetic additives were used as potential crowders: Triethylene glycol (TEG), polyethylene glycol (PEG), Ficoll 400 as a highly branched polysaccharide, and sucrose corresponding to the monomeric unit of Ficoll. Combined UV/Vis spectroscopy and time-resolved light scattering revealed a strong impact of crowding based on excluded volume effects only for Ficoll 400. Sucrose had hardly any influence on the self-assembly of PIC and PEG and TEG impeded the PIC self-assembly. Development of such a PIC based model system led over to in-cell experiments. HeLa cells were infiltrated with PIC solutions well below the aggregation threshold in the infiltrating solution. In the cellular environment, PIC was exposed to a significant crowding and immediately started to aggregate. As was demonstrated by fluorescence imaging, the extent of aggregation can be modulated by exposing the cells to salt-induced osmotic stress. The results suggest future use of such a system as a sensor for the analysis of in vitro and in vivo crowding effects on self-assembly processes.

Identifiants

pubmed: 32154954
doi: 10.1002/chem.202000113
pmc: PMC7317963
doi:

Substances chimiques

Cyanides 0
Macromolecular Substances 0
Ficoll 25702-74-3
triethylene glycol 3P5SU53360
Polyethylene Glycols 3WJQ0SDW1A

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7041-7050

Informations de copyright

© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

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Auteurs

Benjamin Hämisch (B)

Physical Chemistry, Paderborn University, 33098, Paderborn, Germany.

Roland Pollak (R)

Physical and Theoretical Chemistry, TU Braunschweig, 38106, Braunschweig, Germany.

Simon Ebbinghaus (S)

Physical and Theoretical Chemistry, TU Braunschweig, 38106, Braunschweig, Germany.

Klaus Huber (K)

Physical Chemistry, Paderborn University, 33098, Paderborn, Germany.

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Classifications MeSH