Literature DB >> 30905972

Cell Penetration, Herbicidal Activity, and in-vivo-Toxicity of Oligo-Arginine Derivatives and of Novel Guanidinium-Rich Compounds Derived from the Biopolymer Cyanophycin.

Marcel Grogg1, Donald Hilvert1, Marc-Olivier Ebert1, Albert K Beck1, Dieter Seebach1, Felix Kurth2, Petra S Dittrich2, Christof Sparr3, Sergio Wittlin4, Matthias Rottmann4, Pascal Mäser4.   

Abstract

Oligo-arginines are thoroughly studied cell-penetrating peptides (CPPs, Figures 1 and 2). Previous in-vitro investigations with the octaarginine salt of the phosphonate fosmidomycin (herbicide and anti-malaria drug) have shown a 40-fold parasitaemia inhibition with P. falciparum, compared to fosmidomycin alone (Figure 3). We have now tested this salt, as well as the corresponding phosphinate salt of the herbicide glufosinate, for herbicidal activity with whole plants by spray application, hoping for increased activities, i.e. decreased doses. However, both salts showed low herbicidal activity, indicating poor foliar uptake (Table 1). Another pronounced difference between in-vitro and in-vivo activity was demonstrated with various cell-penetrating octaarginine salts of fosmidomycin: intravenous injection to mice caused exitus of the animals within minutes, even at doses as low as 1.4 μmol/kg (Table 2). The results show that use of CPPs for drug delivery, for instance to cancer cells and tissues, must be considered with due care. The biopolymer cyanophycin is a poly-aspartic acid containing argininylated side chains (Figure 4); its building block is the dipeptide H-βAsp-αArg-OH (H-Adp-OH). To test and compare the biological properties with those of octaarginines we synthesized Adp8-derivatives (Figure 5). Intravenouse injection of H-Adp8-NH2 into the tail vein of mice with doses as high as 45 μmol/kg causes no symptoms whatsoever (Table 3), but H-Adp8-NH2 is not cell penetrating (HEK293 and MCF-7 cells, Figure 6). On the other hand, the fluorescently labeled octamers FAM-(Adp(OMe))8-NH2 and FAM-(Adp(NMe2))8-NH2 with ester and amide groups in the side chains exhibit mediocre to high cell-wall permeability (Figure 6), and are toxic (Table 3). Possible reasons for this behavior are discussed (Figure 7) and corresponding NMR spectra are presented (Figure 8).

Entities:  

Keywords:  biopolymer cyanophycin; cell penetration; confocal fluorescence microscopy (CFM); dipeptide Adp (H-βAsp-αArg-OH); fosmidomycin; glufosinate; guanidinium-rich peptides; herbicidal activity; in-vivo toxicity

Year:  2018        PMID: 30905972      PMCID: PMC6426238          DOI: 10.1002/hlca.201800112

Source DB:  PubMed          Journal:  Helv Chim Acta        ISSN: 0018-019X            Impact factor:   2.164


  55 in total

1.  Cellular uptake studies with beta-peptides.

Authors:  Magnus Rueping; Yogesh Mahajan; Markus Sauer; Dieter Seebach
Journal:  Chembiochem       Date:  2002-03-01       Impact factor: 3.164

2.  Artificial Organic Host Molecules for Anions.

Authors:  Franz P. Schmidtchen; Michael Berger
Journal:  Chem Rev       Date:  1997-08-05       Impact factor: 60.622

3.  Bacterial cell penetration by beta3-oligohomoarginines: indications for passive transfer through the lipid bilayer.

Authors:  Birgit Geueke; Kenji Namoto; Irina Agarkova; Jean-Claude Perriard; Hans-Peter E Kohler; Dieter Seebach
Journal:  Chembiochem       Date:  2005-06       Impact factor: 3.164

4.  Characterization of hydrophilic and lipophilic pathways of Hedera helix L. cuticular membranes: permeation of water and uncharged organic compounds.

Authors:  Christian Popp; Markus Burghardt; Adrian Friedmann; Markus Riederer
Journal:  J Exp Bot       Date:  2005-09-05       Impact factor: 6.992

5.  Highly efficient, nonpeptidic oligoguanidinium vectors that selectively internalize into mitochondria.

Authors:  Jimena Fernández-Carneado; Michiel Van Gool; Vera Martos; Susanna Castel; Pilar Prados; Javier de Mendoza; Ernest Giralt
Journal:  J Am Chem Soc       Date:  2005-01-26       Impact factor: 15.419

6.  Conjugation of arginine oligomers to cyclosporin A facilitates topical delivery and inhibition of inflammation.

Authors:  J B Rothbard; S Garlington; Q Lin; T Kirschberg; E Kreider; P L McGrane; P A Wender; P A Khavari
Journal:  Nat Med       Date:  2000-11       Impact factor: 53.440

7.  Tumor imaging by means of proteolytic activation of cell-penetrating peptides.

Authors:  Tao Jiang; Emilia S Olson; Quyen T Nguyen; Melinda Roy; Patricia A Jennings; Roger Y Tsien
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-15       Impact factor: 11.205

8.  Arginine-rich peptides. An abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery.

Authors:  S Futaki; T Suzuki; W Ohashi; T Yagami; S Tanaka; K Ueda; Y Sugiura
Journal:  J Biol Chem       Date:  2000-11-17       Impact factor: 5.157

9.  Arginine magic with new counterions up the sleeve.

Authors:  Masamichi Nishihara; Florent Perret; Toshihide Takeuchi; Shiroh Futaki; Adina N Lazar; Anthony W Coleman; Naomi Sakai; Stefan Matile
Journal:  Org Biomol Chem       Date:  2005-04-07       Impact factor: 3.876

10.  Role of membrane potential and hydrogen bonding in the mechanism of translocation of guanidinium-rich peptides into cells.

Authors:  Jonathan B Rothbard; Theodore C Jessop; Richard S Lewis; Bryce A Murray; Paul A Wender
Journal:  J Am Chem Soc       Date:  2004-08-11       Impact factor: 15.419

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  1 in total

1.  A cryptic third active site in cyanophycin synthetase creates primers for polymerization.

Authors:  Itai Sharon; Sharon Pinus; Marcel Grogg; Nicolas Moitessier; Donald Hilvert; T Martin Schmeing
Journal:  Nat Commun       Date:  2022-07-07       Impact factor: 17.694

  1 in total

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