Cargando…

Enhanced avidin binding to lipid bilayers using PDP-PE lipids with PEG-biotin linkers

Two of the most important aspects of lipid bilayers that have increased their popularity in the field of nanotechnology and biosensors are their fluid nature, which is highly beneficial in ensuring the spatial organization of attached molecules, and the relative ease in which they can be manipulated...

Descripción completa

Detalles Bibliográficos
Autores principales: Birchenough, Holly L., Swann, Marcus J., Zindy, Egor, Day, Anthony J., Jowitt, Thomas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417969/
https://www.ncbi.nlm.nih.gov/pubmed/36132312
http://dx.doi.org/10.1039/d0na00060d
_version_ 1784776843050614784
author Birchenough, Holly L.
Swann, Marcus J.
Zindy, Egor
Day, Anthony J.
Jowitt, Thomas A.
author_facet Birchenough, Holly L.
Swann, Marcus J.
Zindy, Egor
Day, Anthony J.
Jowitt, Thomas A.
author_sort Birchenough, Holly L.
collection PubMed
description Two of the most important aspects of lipid bilayers that have increased their popularity in the field of nanotechnology and biosensors are their fluid nature, which is highly beneficial in ensuring the spatial organization of attached molecules, and the relative ease in which they can be manipulated to change the surface chemistry. Here we have used two different types of functionalized lipids to study the interaction of avidin, which is a common approach to attach further ligands for study. We have tested the commonly used Biotinyl-Cap-PE lipids at different molar percentages and reveal that avidin is not evenly distributed, but forms what looks like clusters even at low percentage occupancy which hampers the level of avidin that can be associated with the surface. We have then successfully employed the novel strategy of using PDP-PE lipids which contain a reducible disulphide to which we added maleamide-PEG-biotin spacers of different lengths. There is a more even distribution of avidin on these layers and thereby increasing the amount and efficiency of avidin association. The reduced levels of avidin that was being associated with the Biotinyl-Cap-PE layers as compared to the PDP-PE lipids could be analysed with QCM-D and interferometry approaches, but it was only with SEEC microscopy that the reason for the reduced occupancy was resolved.
format Online
Article
Text
id pubmed-9417969
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher RSC
record_format MEDLINE/PubMed
spelling pubmed-94179692022-09-20 Enhanced avidin binding to lipid bilayers using PDP-PE lipids with PEG-biotin linkers Birchenough, Holly L. Swann, Marcus J. Zindy, Egor Day, Anthony J. Jowitt, Thomas A. Nanoscale Adv Chemistry Two of the most important aspects of lipid bilayers that have increased their popularity in the field of nanotechnology and biosensors are their fluid nature, which is highly beneficial in ensuring the spatial organization of attached molecules, and the relative ease in which they can be manipulated to change the surface chemistry. Here we have used two different types of functionalized lipids to study the interaction of avidin, which is a common approach to attach further ligands for study. We have tested the commonly used Biotinyl-Cap-PE lipids at different molar percentages and reveal that avidin is not evenly distributed, but forms what looks like clusters even at low percentage occupancy which hampers the level of avidin that can be associated with the surface. We have then successfully employed the novel strategy of using PDP-PE lipids which contain a reducible disulphide to which we added maleamide-PEG-biotin spacers of different lengths. There is a more even distribution of avidin on these layers and thereby increasing the amount and efficiency of avidin association. The reduced levels of avidin that was being associated with the Biotinyl-Cap-PE layers as compared to the PDP-PE lipids could be analysed with QCM-D and interferometry approaches, but it was only with SEEC microscopy that the reason for the reduced occupancy was resolved. RSC 2020-03-10 /pmc/articles/PMC9417969/ /pubmed/36132312 http://dx.doi.org/10.1039/d0na00060d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Birchenough, Holly L.
Swann, Marcus J.
Zindy, Egor
Day, Anthony J.
Jowitt, Thomas A.
Enhanced avidin binding to lipid bilayers using PDP-PE lipids with PEG-biotin linkers
title Enhanced avidin binding to lipid bilayers using PDP-PE lipids with PEG-biotin linkers
title_full Enhanced avidin binding to lipid bilayers using PDP-PE lipids with PEG-biotin linkers
title_fullStr Enhanced avidin binding to lipid bilayers using PDP-PE lipids with PEG-biotin linkers
title_full_unstemmed Enhanced avidin binding to lipid bilayers using PDP-PE lipids with PEG-biotin linkers
title_short Enhanced avidin binding to lipid bilayers using PDP-PE lipids with PEG-biotin linkers
title_sort enhanced avidin binding to lipid bilayers using pdp-pe lipids with peg-biotin linkers
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417969/
https://www.ncbi.nlm.nih.gov/pubmed/36132312
http://dx.doi.org/10.1039/d0na00060d
work_keys_str_mv AT birchenoughhollyl enhancedavidinbindingtolipidbilayersusingpdppelipidswithpegbiotinlinkers
AT swannmarcusj enhancedavidinbindingtolipidbilayersusingpdppelipidswithpegbiotinlinkers
AT zindyegor enhancedavidinbindingtolipidbilayersusingpdppelipidswithpegbiotinlinkers
AT dayanthonyj enhancedavidinbindingtolipidbilayersusingpdppelipidswithpegbiotinlinkers
AT jowittthomasa enhancedavidinbindingtolipidbilayersusingpdppelipidswithpegbiotinlinkers