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The Effects of a Novel Series of KTTKS Analogues on Cytotoxicity and Proteolytic Activity
KTTKS is a matrikine that originates from the proteolytic hydrolysis of collagen. This peptide stimulates ECM production and types I and III collagen expression in vitro. A more stable form of KTTKS is pal-KTTKS, known as Matrixyl(®) or palmitoyl pentapeptide-3. A series of novel pentapeptides, anal...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832239/ https://www.ncbi.nlm.nih.gov/pubmed/31618846 http://dx.doi.org/10.3390/molecules24203698 |
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author | Tałałaj, Urszula Uścinowicz, Paulina Bruzgo, Irena Surażyński, Arkadiusz Zaręba, Ilona Markowska, Agnieszka |
author_facet | Tałałaj, Urszula Uścinowicz, Paulina Bruzgo, Irena Surażyński, Arkadiusz Zaręba, Ilona Markowska, Agnieszka |
author_sort | Tałałaj, Urszula |
collection | PubMed |
description | KTTKS is a matrikine that originates from the proteolytic hydrolysis of collagen. This peptide stimulates ECM production and types I and III collagen expression in vitro. A more stable form of KTTKS is pal-KTTKS, known as Matrixyl(®) or palmitoyl pentapeptide-3. A series of novel pentapeptides, analogues of KTTKS with the general formula X-KTTKS-OH(NH(2)), where X = acetyl, lipoyl, palmitoyl residues, was designed and synthesized. Their effect on amidolytic activity of urokinase, thrombin, trypsin, plasmin, t-PA, and kallikrein were tested. Cytotoxic tests on fibroblasts, as well as collagen and DNA biosynthesis tests for selected peptides, were also carried out. The test results showed that the most active plasmin inhibitors were palmitoyl peptides, whether in acid or amide form. No biological effects of lysine modification to arginine in the synthesized peptides were found. None of the synthesized peptides was not cytotoxic on fibroblasts, and three of them showed cell growth. These three compounds showed no concentration-activity relationship in the collagen and DNA biosynthesis assays. |
format | Online Article Text |
id | pubmed-6832239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68322392019-11-21 The Effects of a Novel Series of KTTKS Analogues on Cytotoxicity and Proteolytic Activity Tałałaj, Urszula Uścinowicz, Paulina Bruzgo, Irena Surażyński, Arkadiusz Zaręba, Ilona Markowska, Agnieszka Molecules Article KTTKS is a matrikine that originates from the proteolytic hydrolysis of collagen. This peptide stimulates ECM production and types I and III collagen expression in vitro. A more stable form of KTTKS is pal-KTTKS, known as Matrixyl(®) or palmitoyl pentapeptide-3. A series of novel pentapeptides, analogues of KTTKS with the general formula X-KTTKS-OH(NH(2)), where X = acetyl, lipoyl, palmitoyl residues, was designed and synthesized. Their effect on amidolytic activity of urokinase, thrombin, trypsin, plasmin, t-PA, and kallikrein were tested. Cytotoxic tests on fibroblasts, as well as collagen and DNA biosynthesis tests for selected peptides, were also carried out. The test results showed that the most active plasmin inhibitors were palmitoyl peptides, whether in acid or amide form. No biological effects of lysine modification to arginine in the synthesized peptides were found. None of the synthesized peptides was not cytotoxic on fibroblasts, and three of them showed cell growth. These three compounds showed no concentration-activity relationship in the collagen and DNA biosynthesis assays. MDPI 2019-10-15 /pmc/articles/PMC6832239/ /pubmed/31618846 http://dx.doi.org/10.3390/molecules24203698 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tałałaj, Urszula Uścinowicz, Paulina Bruzgo, Irena Surażyński, Arkadiusz Zaręba, Ilona Markowska, Agnieszka The Effects of a Novel Series of KTTKS Analogues on Cytotoxicity and Proteolytic Activity |
title | The Effects of a Novel Series of KTTKS Analogues on Cytotoxicity and Proteolytic Activity |
title_full | The Effects of a Novel Series of KTTKS Analogues on Cytotoxicity and Proteolytic Activity |
title_fullStr | The Effects of a Novel Series of KTTKS Analogues on Cytotoxicity and Proteolytic Activity |
title_full_unstemmed | The Effects of a Novel Series of KTTKS Analogues on Cytotoxicity and Proteolytic Activity |
title_short | The Effects of a Novel Series of KTTKS Analogues on Cytotoxicity and Proteolytic Activity |
title_sort | effects of a novel series of kttks analogues on cytotoxicity and proteolytic activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832239/ https://www.ncbi.nlm.nih.gov/pubmed/31618846 http://dx.doi.org/10.3390/molecules24203698 |
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