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Application of Alanine Scanning to Determination of Amino Acids Essential for Peptide Adsorption at the Solid/Solution Interface and Binding to the Receptor: Surface-Enhanced Raman/Infrared Spectroscopy versus Bioactivity Assays
[Image: see text] The article describes the application of the alanine-scanning technique used in combination with Raman, surface-enhanced Raman, attenuated total reflection Fourier transform infrared, and surface-enhanced infrared absorption (SEIRA) spectroscopies, which allowed defining the role o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279479/ https://www.ncbi.nlm.nih.gov/pubmed/34110823 http://dx.doi.org/10.1021/acs.jmedchem.1c00397 |
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author | Proniewicz, Edyta Burnat, Grzegorz Domin, Helena Małuch, Izabela Makowska, Marta Prahl, Adam |
author_facet | Proniewicz, Edyta Burnat, Grzegorz Domin, Helena Małuch, Izabela Makowska, Marta Prahl, Adam |
author_sort | Proniewicz, Edyta |
collection | PubMed |
description | [Image: see text] The article describes the application of the alanine-scanning technique used in combination with Raman, surface-enhanced Raman, attenuated total reflection Fourier transform infrared, and surface-enhanced infrared absorption (SEIRA) spectroscopies, which allowed defining the role of individual amino acid residues in the C-terminal 6–14 fragment of the bombesin chain (BN(6–14)) on the path of its adsorption on the surface of Ag (AgNPs) and Au nanoparticles (AuNPs). A reliable analysis of the SEIRA spectra of these peptides was possible, thanks to a curve fitting of these spectra. By combining alanine-scanning with biological activity studies using cell lines overexpressing bombesin receptors and the intracellular inositol monophosphate assay, it was possible to determine which peptide side chains play a significant role in binding a peptide to membrane-bound G protein-coupled receptors (GPCRs). Based on the analysis of spectral profiles and bioactivity results, conclusions for the specific peptide–metal and peptide–GPCR interactions were drawn and compared. |
format | Online Article Text |
id | pubmed-8279479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82794792021-07-15 Application of Alanine Scanning to Determination of Amino Acids Essential for Peptide Adsorption at the Solid/Solution Interface and Binding to the Receptor: Surface-Enhanced Raman/Infrared Spectroscopy versus Bioactivity Assays Proniewicz, Edyta Burnat, Grzegorz Domin, Helena Małuch, Izabela Makowska, Marta Prahl, Adam J Med Chem [Image: see text] The article describes the application of the alanine-scanning technique used in combination with Raman, surface-enhanced Raman, attenuated total reflection Fourier transform infrared, and surface-enhanced infrared absorption (SEIRA) spectroscopies, which allowed defining the role of individual amino acid residues in the C-terminal 6–14 fragment of the bombesin chain (BN(6–14)) on the path of its adsorption on the surface of Ag (AgNPs) and Au nanoparticles (AuNPs). A reliable analysis of the SEIRA spectra of these peptides was possible, thanks to a curve fitting of these spectra. By combining alanine-scanning with biological activity studies using cell lines overexpressing bombesin receptors and the intracellular inositol monophosphate assay, it was possible to determine which peptide side chains play a significant role in binding a peptide to membrane-bound G protein-coupled receptors (GPCRs). Based on the analysis of spectral profiles and bioactivity results, conclusions for the specific peptide–metal and peptide–GPCR interactions were drawn and compared. American Chemical Society 2021-06-10 2021-06-24 /pmc/articles/PMC8279479/ /pubmed/34110823 http://dx.doi.org/10.1021/acs.jmedchem.1c00397 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Proniewicz, Edyta Burnat, Grzegorz Domin, Helena Małuch, Izabela Makowska, Marta Prahl, Adam Application of Alanine Scanning to Determination of Amino Acids Essential for Peptide Adsorption at the Solid/Solution Interface and Binding to the Receptor: Surface-Enhanced Raman/Infrared Spectroscopy versus Bioactivity Assays |
title | Application of
Alanine Scanning to Determination of
Amino Acids Essential for Peptide Adsorption at the Solid/Solution
Interface and Binding to the Receptor: Surface-Enhanced Raman/Infrared
Spectroscopy versus Bioactivity Assays |
title_full | Application of
Alanine Scanning to Determination of
Amino Acids Essential for Peptide Adsorption at the Solid/Solution
Interface and Binding to the Receptor: Surface-Enhanced Raman/Infrared
Spectroscopy versus Bioactivity Assays |
title_fullStr | Application of
Alanine Scanning to Determination of
Amino Acids Essential for Peptide Adsorption at the Solid/Solution
Interface and Binding to the Receptor: Surface-Enhanced Raman/Infrared
Spectroscopy versus Bioactivity Assays |
title_full_unstemmed | Application of
Alanine Scanning to Determination of
Amino Acids Essential for Peptide Adsorption at the Solid/Solution
Interface and Binding to the Receptor: Surface-Enhanced Raman/Infrared
Spectroscopy versus Bioactivity Assays |
title_short | Application of
Alanine Scanning to Determination of
Amino Acids Essential for Peptide Adsorption at the Solid/Solution
Interface and Binding to the Receptor: Surface-Enhanced Raman/Infrared
Spectroscopy versus Bioactivity Assays |
title_sort | application of
alanine scanning to determination of
amino acids essential for peptide adsorption at the solid/solution
interface and binding to the receptor: surface-enhanced raman/infrared
spectroscopy versus bioactivity assays |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8279479/ https://www.ncbi.nlm.nih.gov/pubmed/34110823 http://dx.doi.org/10.1021/acs.jmedchem.1c00397 |
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