Targeted Chemical Modifications Identify Key Features of Carbohydrate Assemblies and Generate Tailored Carbohydrate Materials.

carbohydrates electron diffraction electron tomography site-specific modifications supramolecular assemblies

Journal

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

Informations de publication

Date de publication:
15 Sep 2021
Historique:
received: 17 06 2021
pubmed: 13 7 2021
medline: 18 9 2021
entrez: 12 7 2021
Statut: ppublish

Résumé

The molecular level description of carbohydrate assemblies is hampered by their structural complexity and the lack of suitable analytical methods. Here, we employed systematic chemical modifications to identify key non-covalent interactions that triggered the supramolecular assembly of a disaccharide model. While some modifications disrupted the supramolecular organization, others were tolerated, delivering important information on the aggregation process. The screening identified new geometries, including nanotubes, and twisted ribbons that were characterized with electron tomography and electron diffraction (ED) methods. This work demonstrates that the combination of synthetic chemistry and ED methods is a powerful tool to draw correlations between the molecular structure and the nanoscale architecture of carbohydrate assemblies.

Identifiants

pubmed: 34251709
doi: 10.1002/chem.202102164
pmc: PMC8518775
doi:

Substances chimiques

Carbohydrates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

13139-13143

Subventions

Organisme : max-planck-gesellschaft
Organisme : bundesministerium für bildung und forschung
ID : 13XP5114
Organisme : deutsche forschungsgemeinschaft
ID : SFB 1449
Organisme : cdp glyco@alps
ID : ANR-15-IDEX-02
Organisme : nanobio-icmg platform
ID : FR 2607

Informations de copyright

© 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.

Références

Chem Soc Rev. 2010 Jun;39(6):1877-90
pubmed: 20502791
Chem Rev. 2016 Feb 24;116(4):1693-752
pubmed: 26702928
Chem Rev. 2010 Jun 9;110(6):3479-500
pubmed: 20201500
Gels. 2021 Feb 26;7(1):
pubmed: 33652820
Science. 2002 Mar 29;295(5564):2418-21
pubmed: 11923529
Annu Rev Biochem. 2009;78:929-58
pubmed: 19344236
Langmuir. 2012 Aug 28;28(34):12609-18
pubmed: 22852550
J Org Chem. 2020 Dec 18;85(24):16072-16081
pubmed: 33258593
Chembiochem. 2004 May 3;5(5):622-7
pubmed: 15122633
Chem Rev. 2018 Sep 12;118(17):8005-8024
pubmed: 30091597
Nat Chem Biol. 2007 May;3(5):252-62
pubmed: 17438550
Chem Sci. 2018 Dec 21;10(8):2385-2390
pubmed: 30881666
Chem Soc Rev. 2018 May 21;47(10):3406-3420
pubmed: 29498728
Angew Chem Int Ed Engl. 2019 Sep 9;58(37):13127-13132
pubmed: 31359577
J Am Chem Soc. 2007 Mar 14;129(10):2890-900
pubmed: 17309255
Chem Rev. 2002 Feb;102(2):371-86
pubmed: 11841247
Chemistry. 2021 Sep 15;27(52):13139-13143
pubmed: 34251709
Science. 2019 Mar 29;363(6434):1396-1397
pubmed: 30923212
Acc Chem Res. 2013 Apr 16;46(4):946-54
pubmed: 22704792
Chemistry. 2020 Sep 4;26(50):11643-11655
pubmed: 32333713
J Biol Chem. 2015 Jul 31;290(31):19334-42
pubmed: 26092728
Nature. 2021 Feb;590(7844):47-56
pubmed: 33536649
J Am Chem Soc. 2020 Oct 7;142(40):17015-17023
pubmed: 32946227
Adv Mater. 2016 Jul;28(26):5262-7
pubmed: 27152434
Acc Chem Res. 2013 Apr 16;46(4):907-15
pubmed: 23095018
J Am Chem Soc. 2009 Dec 23;131(50):18129-38
pubmed: 19928848
Nanoscale Horiz. 2017 Nov 1;2(6):342-348
pubmed: 32260664
Chem Rev. 2015 Dec 23;115(24):13165-307
pubmed: 26646318
Acc Chem Res. 2014 Jun 17;47(6):1871-80
pubmed: 24856178
Glycoconj J. 2004;21(3-4):149-63
pubmed: 15483380
Chem Soc Rev. 2008 Feb;37(2):320-30
pubmed: 18197348
J Am Chem Soc. 2019 Mar 27;141(12):4833-4838
pubmed: 30829477
ACS Nano. 2017 Jun 27;11(6):5960-5969
pubmed: 28575577
J Am Chem Soc. 2021 May 5;143(17):6622-6633
pubmed: 33900761
Chem Soc Rev. 2020 Jun 22;49(12):3863-3888
pubmed: 32520059
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2019 Sep;11(5):e1558
pubmed: 31063240
Org Biomol Chem. 2020 Feb 19;18(7):1349-1353
pubmed: 32037424

Auteurs

Soeun Gim (S)

Department of Biomolecular Systems, Max-Planck-Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.
Department of Chemistry and Biochemistry, Freie Universität Berlin, Arnimallee 22, 14195, Berlin, Germany.

Giulio Fittolani (G)

Department of Biomolecular Systems, Max-Planck-Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.
Department of Chemistry and Biochemistry, Freie Universität Berlin, Arnimallee 22, 14195, Berlin, Germany.

Yang Yu (Y)

Department of Biomolecular Systems, Max-Planck-Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.
Simpson Querrey Institute, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208, USA.

Yuntao Zhu (Y)

Department of Biomolecular Systems, Max-Planck-Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.

Peter H Seeberger (PH)

Department of Biomolecular Systems, Max-Planck-Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.
Department of Chemistry and Biochemistry, Freie Universität Berlin, Arnimallee 22, 14195, Berlin, Germany.

Yu Ogawa (Y)

Univ. Grenoble Alpes, CNRS, CERMAV, 38000, Grenoble, France.

Martina Delbianco (M)

Department of Biomolecular Systems, Max-Planck-Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.

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