Cargando…
Model of Environmental Membrane Field for Transmembrane Proteins
The water environment determines the activity of biological processes. The role of such an environment interpreted in the form of an external field expressed by the 3D Gaussian distribution in the fuzzy oil drop model directs the folding process towards the generation of a centrally located hydropho...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036355/ https://www.ncbi.nlm.nih.gov/pubmed/33807215 http://dx.doi.org/10.3390/ijms22073619 |
_version_ | 1783676890669645824 |
---|---|
author | Roterman, Irena Stapor, Katarzyna Fabian, Piotr Konieczny, Leszek Banach, Mateusz |
author_facet | Roterman, Irena Stapor, Katarzyna Fabian, Piotr Konieczny, Leszek Banach, Mateusz |
author_sort | Roterman, Irena |
collection | PubMed |
description | The water environment determines the activity of biological processes. The role of such an environment interpreted in the form of an external field expressed by the 3D Gaussian distribution in the fuzzy oil drop model directs the folding process towards the generation of a centrally located hydrophobic core with the simultaneous exposure of polar residues on the surface. In addition to proteins soluble in the water environment, there is a significant group of membrane proteins that act as receptors or channels, including ion channels in particular. The change of the polar (water) environment into a highly hydrophobic (membrane) environment is quite radical, resulting in a different hydrophobicity distribution within the membrane protein. Modification of the notation of the force field expressing the presence of the hydrophobic environment has been proposed in this work. A modified fuzzy oil drop model with its adaptation to membrane proteins was used to interpret the structure of membrane proteins–mechanosensitive channel. The modified model was also used to describe the so-called negative cases—i.e., for water-soluble proteins with a clear distribution consistent with the fuzzy oil drop model. |
format | Online Article Text |
id | pubmed-8036355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80363552021-04-12 Model of Environmental Membrane Field for Transmembrane Proteins Roterman, Irena Stapor, Katarzyna Fabian, Piotr Konieczny, Leszek Banach, Mateusz Int J Mol Sci Article The water environment determines the activity of biological processes. The role of such an environment interpreted in the form of an external field expressed by the 3D Gaussian distribution in the fuzzy oil drop model directs the folding process towards the generation of a centrally located hydrophobic core with the simultaneous exposure of polar residues on the surface. In addition to proteins soluble in the water environment, there is a significant group of membrane proteins that act as receptors or channels, including ion channels in particular. The change of the polar (water) environment into a highly hydrophobic (membrane) environment is quite radical, resulting in a different hydrophobicity distribution within the membrane protein. Modification of the notation of the force field expressing the presence of the hydrophobic environment has been proposed in this work. A modified fuzzy oil drop model with its adaptation to membrane proteins was used to interpret the structure of membrane proteins–mechanosensitive channel. The modified model was also used to describe the so-called negative cases—i.e., for water-soluble proteins with a clear distribution consistent with the fuzzy oil drop model. MDPI 2021-03-31 /pmc/articles/PMC8036355/ /pubmed/33807215 http://dx.doi.org/10.3390/ijms22073619 Text en © 2021 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 | Article Roterman, Irena Stapor, Katarzyna Fabian, Piotr Konieczny, Leszek Banach, Mateusz Model of Environmental Membrane Field for Transmembrane Proteins |
title | Model of Environmental Membrane Field for Transmembrane Proteins |
title_full | Model of Environmental Membrane Field for Transmembrane Proteins |
title_fullStr | Model of Environmental Membrane Field for Transmembrane Proteins |
title_full_unstemmed | Model of Environmental Membrane Field for Transmembrane Proteins |
title_short | Model of Environmental Membrane Field for Transmembrane Proteins |
title_sort | model of environmental membrane field for transmembrane proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8036355/ https://www.ncbi.nlm.nih.gov/pubmed/33807215 http://dx.doi.org/10.3390/ijms22073619 |
work_keys_str_mv | AT rotermanirena modelofenvironmentalmembranefieldfortransmembraneproteins AT staporkatarzyna modelofenvironmentalmembranefieldfortransmembraneproteins AT fabianpiotr modelofenvironmentalmembranefieldfortransmembraneproteins AT koniecznyleszek modelofenvironmentalmembranefieldfortransmembraneproteins AT banachmateusz modelofenvironmentalmembranefieldfortransmembraneproteins |