From Distinct Metallopeptoids to Self-Assembled Supramolecular Architectures.

copper metallopeptoids peptides peptoids supramolecular framework

Journal

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

Informations de publication

Date de publication:
07 Jan 2021
Historique:
received: 04 08 2020
revised: 25 08 2020
pubmed: 28 8 2020
medline: 28 8 2020
entrez: 28 8 2020
Statut: ppublish

Résumé

The construction of synthetic protein mimics is a central goal in chemistry. A known approach for achieving this goal is the self-assembly of synthetic biomimetic sequences into supramolecular structures. Obtaining different 3D structures via a simple sequence modification, however, is still challenging. Herein we present the design and synthesis of biomimetic architectures, via the self-assembly of distinct copper-peptoid duplexes. We demonstrate that changing only one non-coordinating side-chain within the peptoids-sequence-specific N-substituted glycine oligomers-leads to different supramolecular structures. Four peptoid trimers incorporating 2,2'-bipyridine and pyridine ligands, and a non-coordinating but rather a structure-directed bulky group were synthesized, and their solutions were treated with Cu

Identifiants

pubmed: 32853428
doi: 10.1002/chem.202003612
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

634-640

Subventions

Organisme : Israel Science Foundation
ID : 395/16

Informations de copyright

© 2020 Wiley-VCH GmbH.

Références

 
C. Hu, S. I. Chan, E. B. Sawyer, Y. Yu, J. Wang, Chem. Soc. Rev. 2014, 43, 6498;
J. Li, Supramolecular Chemistry of Biomimetic Systems, 2017, Springer Singapore.
 
L. A. Churchfield, R. G. Alberstein, L. M. Williamson, F. A. Tezcan, J. Am. Chem. Soc. 2018, 140, 10043;
J. Rittle, M. J. Field, M. T. Green, F. A. Tezcan, Nat. Chem. 2019, 11, 434;
H. Li, S. H. Park, J. H. Reif, T. H. LaBean, H. Yan, J. Am. Chem. Soc. 2004, 126, 418;
E. R. Ballister, A. H. Lai, R. N. Zuckermann, Y. Cheng, J. D. Mougous, Proc. Natl. Acad. Sci. USA 2008, 105, 3733;
M. L. Zastrow, A. F. A. Peacock, J. A. Stuckey, V. L. Pecoraro, Nat. Chem. 2012, 4, 118.
 
D. Bousmail, P. Chidchob, H. F. Sleiman, J. Am. Chem. Soc. 2018, 140, 9518-9530;
P. Chidchob, D. Offenbartl-Stiegert, D. McCarthy, X. Luo, J. Li, S. Howorka, H. F. Sleiman, J. Am. Chem. Soc. 2019, 141, 1100.
 
T. Sawada, M. Yamagami, K. Ohara, K. Yamaguchi, M. Fujita, Angew. Chem. Int. Ed. 2016, 55, 4519;
Angew. Chem. 2016, 128, 4595;
T. Sawada, M. Yamagami, S. Akinaga, T. Miyaji, M. Fujita, Chem. Asian J. 2017, 12, 1715;
T. Sawada, A. Matsumoto, M. Fujita, Angew. Chem. Int. Ed. 2014, 53, 7228;
Angew. Chem. 2014, 126, 7356;
X. Fu, Y. Wang, L. Huang, Y. Sha, L. Gui, L. Lai, Y. Tang, Adv. Mater. 2003, 15, 902;
S. Kwon, H. S. Shin, J. Gong, J. H. Eom, A. Jeon, S. H. Yoo, I. S. Chung, S. J. Cho, H. S. Lee, J. Am. Chem. Soc. 2011, 133, 17618.
 
J. Sun, X. Jiang, R. Lund, K. H. Downing, N. P. Balsara, R. N. Zuckermann, Proc. Natl. Acad. Sci. USA 2016, 113, 3954;
H. A. Lashuel, S. R. LaBrenz, L. Woo, L. C. Serpell, J. W. Kelly, J. Am. Chem. Soc. 2000, 122, 5262;
H. K. Murnen, A. M. Rosales, J. N. Jaworski, R. A. Segalman, R. N. Zuckermann, J. Am. Chem. Soc. 2010, 132, 16112;
J. Kim, S. Kwon, S. H. Kim, C. K. Lee, J. H. Lee, S. J. Cho, H. S. Lee, H. Ihee, J. Am. Chem. Soc. 2012, 134, 20573.
 
G. Maayan, M. D. Ward, K. Kirshenbaum, Chem. Commun. 2009, 56;
T. Zabrodski, M. Baskin, P. J. Kaniraj, G. Maayan, Synlett 2015, 26, 461;
M. Baskin, G. Maayan, Biopolymers 2015, 104, 577;
M. Baskin, G. Maayan, Chem. Sci. 2016, 7, 2809;
M. Baskin, L. Panz, G. Maayan, Chem. Commun. 2016, 52, 10350;
L. Zborovsky, A. Smolyakova, M. Baskin, G. Maayan, Chem. Eur. J. 2018, 24, 1159;
M. Baskin, G. Maayan, Dalton Trans. 2018, 47, 10767;
M. Baskin, H. Zhu, Z.-W. Qu, J. H. Chill, S. Grimme, G. Maayan, Chem. Sci. 2019, 10, 620;
L. Zborovsky, H. Tigger-Zaborov, G. Maayan, Chem. Eur. J. 2019, 25, 9098;
C. De Cola, S. Licen, D. Comegna, E. Cafaro, G. Bifulco, I. Izzo, P. Tecilla, F. De Riccardis, Org. Biomol. Chem. 2009, 7, 2851;
C. Tedesco, L. Erra, I. Izzo, F. De Riccardis, Cryst. Eng. Comm. 2014, 16, 3667.
 
H. Tigger-Zaborov, G. Maayan, J. Colloid Interface Sci. 2017, 508, 56;
T. Ghosh, N. Fridman, M. Kosa, G. Maayan, Angew. Chem. Int. Ed. 2018, 57, 7703;
Angew. Chem. 2018, 130, 7829;
H. Tigger-Zaborov, G. Maayan, J. Coll. Inter. Sci. 2019, 533, 598.
 
R. V. Mannige, T. K. Haxton, C. Proulx, E. J. Robertson, A. Battigelli, G. L. Butterfoss, R. N. Zuckermann, S. Whitelam, Nature 2015, 526, 415;
K. T. Nam, S. A. Shelby, P. H. Choi, A. B. Marciel, R. Chen, L. Tan, T. K. Chu, R. A. Mesch, B. C. Lee, M. D. Connolly, Nat. Mater. 2010, 9, 454;
C. Tedesco, E. Macedi, A. Meli, G. Pierri, G. Della Sala, C. Drathen, A. N. Fitch, G. B. M. Vaughan, I. Izzo, F. De Riccardis, Acta Crystallogr. Sect. B 2017, 73, 399;
S. Xuana, X. Jiangb, R. K. Spencer, N. K. Li, D. Prendergast, N. P. Balsara, R. N. Zuckermann, Proc. Natl. Acad. Sci. USA 2019, 116, 22491.
 
E. Macedi, A. Meli, F. De Riccardis, P. Rossi, V. J. Smith, L. J. Barbour, I. Izzo, C. Tedesco, Cryst. Eng. Comm 2017, 19, 4704;
H. Jin, F. Jiao, M. D. Daily, Y. Chen, F. Yan, Y.-H. Ding, X. Zhang, E. J. Robertson, M. D. Baer, C.-L. Chen, Nat. Commun. 2016, 7, 12252.
S. B. L. Vollrath, C. Hu, S. Bräse, K. Kirshenbaum, Chem. Commun. 2013, 49, 2317.
J. Navarro-Sánchez, A. I. Argente-García, Y. Moliner-Martínez, D. Roca-Sanjuán, D. Antypov, P. Campíns-Falcó, M. J. Rosseinsky, C. Martí-Gastaldo, J. Am. Chem. Soc. 2017, 139, 4294.
 
A. B. Waight, J. Love, D. N. Wang, Nat. Struct. Mol. Biol. 2010, 17, 31;
H. Li, W. H. Hallows, J. S. Punzi, V. E. Marquez, H. L. Carrell, K. W. Pankiewicz, K. A. Watanabe, B. M. Goldstein, Biochemistry 1994, 33, 23.
 
J. R. Stringer, J. A. Crapster, I. A. Guzei, H. E. Blackwell, J. Am. Chem. Soc. 2011, 133, 15559;
K. Kirshenbaum, A. E. Barron, R. A. Goldsmith, P. Armand, E. K. Bradley, K. T. V. Truong, K. A. Dill, F. E. Cohen, R. N. Zuckermann, Proc. Natl. Acad. Sci. 1998, 95, 4303.
 
C. W. Wu, K. Kirshenbaum, T. J. Sanborn, J. A. Patch, K. Huang, K. A. Dill, R. N. Zuckermann, A. E. Barron, J. Am. Chem. Soc. 2003, 125, 13525;
O. Roy, G. Dumonteil, S. Faure, L. Jouffret, A. Kriznik, C. Taillefumier, J. Am. Chem. Soc. 2017, 139, 13533.
 
K. J. Prathap, G. Maayan, Chem. Commun. 2015, 51, 11096;
D. Chandra Mohan, A. Sadhukha, G. Maayan, J. Catal. 2017, 355, 139.
R. N. Zuckermann, J. M. Kerr, W. H. Moosf, S. B. H. Kent, J. Am. Chem. Soc. 1992, 114, 10646.
T. Ghosh, P. Ghosh, G. Maayan, ACS Catal. 2018, 8, 10631.
G. Maayan, Eur. J Org. Chem. 2009, 2009, 5699.
N. Berova, L. Di Bari, G. Pescitelli, Chem. Soc. Rev. 2007, 36, 914.
 
K. Das, A. Datta, C. Sinha, J.-H. Huang, E. Garribba, C.-S. Hsiao, C.-L. Hsu, ChemistryOpen 2012, 1, 80;
P. Mateus, R. Delgado, V. André, M. T. Duarte, Inorg. Chem. 2015, 54, 229.
B. Dhakshnamoorthy, B. K. Ziervogel, L. Blachowicz, B. Roux, J. Am. Chem. Soc. 2013, 135, 16561.
W. Li, J. Li, M. Lee, Chem. Commun. 2013, 49, 8238.
 
G. A. Breault, C. A. Hunter, P. C. Mayers, J. Am. Chem. Soc. 1998, 120, 3402;
J. Q. Nguyen, B. L. Iverson, J. Am. Chem. Soc. 1999, 121, 2639.
 
M. J. Langton, C. J. Serpell, P. D. Beer, Angew. Chem. Int. Ed. 2016, 55, 1974;
Angew. Chem. 2016, 128, 2012;
M. Lisbjerg, H. Valkenier, B. M. Jessen, H. Al-Kerdi, A. P. Davis, M. Pittelkow, J. Am. Chem. Soc. 2015, 137, 4948.
 
Y. Kawano, D. E. Cohen, J. Gastroenterol 2013, 48, 434-441;
B. A. Griffin, Surgery Oxford 2013, 31, 267-272.
L. Zhang, A. J. Stephens, J.-F. Lemonnier, L. Pirvu, I. J. V. Yrezabal, C. J. Robinson, D. A. Leigh, J. Am. Chem. Soc. 2019, 141, 3952-3958.
 
J. S. Laursen, J. Engel-Andreasen, C. A. Olsen, Acc. Chem. Res. 2015, 48, 2696;
C. A. Olsen, Biopolymers 2011, 96, 561;
G. Maayan, M. Albrecht, Metallofoldamers. Supramolecular Architectures from Helicates to Biomimetics, Wiley, Hoboken, 2013;
G. Guichard, I. Huc, Chem. Commun. 2011, 47, 5933;
D. Seebach, J. Gardiner, Acc. Chem. Res. 2008, 41, 1366;
S. Hecht, I. Huc, Foldamers: Structure, Properties, and Applications, Wiley-VCH, Weinheim, 2007;
D. J. Hill, M. J. Mio, R. B. Prince, T. S. Hughes, J. S. Moore, Chem. Rev. 2001, 101, 3893;
S. H. Gellman, Acc. Chem. Res. 1998, 31, 173.

Auteurs

Pritam Ghosh (P)

Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa, 3200008, Israel.

Natalia Fridman (N)

Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa, 3200008, Israel.

Galia Maayan (G)

Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa, 3200008, Israel.

Classifications MeSH