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Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets
The action of proteases can be controlled by several mechanisms, including regulation through gene expression; post-translational modifications, such as glycosylation; zymogen activation; targeting specific compartments, such as lysosomes and mitochondria; and blocking proteolysis using endogenous i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100506/ https://www.ncbi.nlm.nih.gov/pubmed/35563133 http://dx.doi.org/10.3390/ijms23094742 |
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author | Bonturi, Camila Ramalho Silva Teixeira, Ana Beatriz Rocha, Vitória Morais Valente, Penélope Ferreira Oliveira, Juliana Rodrigues Filho, Clovis Macêdo Bezerra Fátima Correia Batista, Isabel Oliva, Maria Luiza Vilela |
author_facet | Bonturi, Camila Ramalho Silva Teixeira, Ana Beatriz Rocha, Vitória Morais Valente, Penélope Ferreira Oliveira, Juliana Rodrigues Filho, Clovis Macêdo Bezerra Fátima Correia Batista, Isabel Oliva, Maria Luiza Vilela |
author_sort | Bonturi, Camila Ramalho |
collection | PubMed |
description | The action of proteases can be controlled by several mechanisms, including regulation through gene expression; post-translational modifications, such as glycosylation; zymogen activation; targeting specific compartments, such as lysosomes and mitochondria; and blocking proteolysis using endogenous inhibitors. Protease inhibitors are important molecules to be explored for the control of proteolytic processes in organisms because of their ability to act on several proteases. In this context, plants synthesize numerous proteins that contribute to protection against attacks by microorganisms (fungi and bacteria) and/or invertebrates (insects and nematodes) through the inhibition of proteases in these organisms. These proteins are widely distributed in the plant kingdom, and are present in higher concentrations in legume seeds (compared to other organs and other botanical families), motivating studies on their inhibitory effects in various organisms, including humans. In most cases, the biological roles of these proteins have been assigned based mostly on their in vitro action, as is the case with enzyme inhibitors. This review highlights the structural evolution, function, and wide variety of effects of plant Kunitz protease inhibitors, and their potential for pharmaceutical application based on their interactions with different proteases. |
format | Online Article Text |
id | pubmed-9100506 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91005062022-05-14 Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets Bonturi, Camila Ramalho Silva Teixeira, Ana Beatriz Rocha, Vitória Morais Valente, Penélope Ferreira Oliveira, Juliana Rodrigues Filho, Clovis Macêdo Bezerra Fátima Correia Batista, Isabel Oliva, Maria Luiza Vilela Int J Mol Sci Review The action of proteases can be controlled by several mechanisms, including regulation through gene expression; post-translational modifications, such as glycosylation; zymogen activation; targeting specific compartments, such as lysosomes and mitochondria; and blocking proteolysis using endogenous inhibitors. Protease inhibitors are important molecules to be explored for the control of proteolytic processes in organisms because of their ability to act on several proteases. In this context, plants synthesize numerous proteins that contribute to protection against attacks by microorganisms (fungi and bacteria) and/or invertebrates (insects and nematodes) through the inhibition of proteases in these organisms. These proteins are widely distributed in the plant kingdom, and are present in higher concentrations in legume seeds (compared to other organs and other botanical families), motivating studies on their inhibitory effects in various organisms, including humans. In most cases, the biological roles of these proteins have been assigned based mostly on their in vitro action, as is the case with enzyme inhibitors. This review highlights the structural evolution, function, and wide variety of effects of plant Kunitz protease inhibitors, and their potential for pharmaceutical application based on their interactions with different proteases. MDPI 2022-04-25 /pmc/articles/PMC9100506/ /pubmed/35563133 http://dx.doi.org/10.3390/ijms23094742 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Bonturi, Camila Ramalho Silva Teixeira, Ana Beatriz Rocha, Vitória Morais Valente, Penélope Ferreira Oliveira, Juliana Rodrigues Filho, Clovis Macêdo Bezerra Fátima Correia Batista, Isabel Oliva, Maria Luiza Vilela Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets |
title | Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets |
title_full | Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets |
title_fullStr | Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets |
title_full_unstemmed | Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets |
title_short | Plant Kunitz Inhibitors and Their Interaction with Proteases: Current and Potential Pharmacological Targets |
title_sort | plant kunitz inhibitors and their interaction with proteases: current and potential pharmacological targets |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9100506/ https://www.ncbi.nlm.nih.gov/pubmed/35563133 http://dx.doi.org/10.3390/ijms23094742 |
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