Label-free measurements of the diffusivity of molecules in lipid membranes
(2014) In ChemPhysChem 15(3). p.91-486- Abstract
An important and characteristic property of a cell membrane is the lateral mobility of protein molecules in the lipid bilayer. This has conventionally been measured by labeling the molecules with fluorescent markers and monitoring their mobility by different fluorescence-based techniques. However, adding the label to the studied molecule may affect the system, so it is an assumption in almost all experiments that the measured mobility of the biomolecule with its label is the same as that of the unlabeled molecule. However, this assumption is rarely tested due to a lack of suitable methods. In this work, a new technique to perform label-free diffusivity measurements is developed and used to measure the effect of the label for two common... (More)
An important and characteristic property of a cell membrane is the lateral mobility of protein molecules in the lipid bilayer. This has conventionally been measured by labeling the molecules with fluorescent markers and monitoring their mobility by different fluorescence-based techniques. However, adding the label to the studied molecule may affect the system, so it is an assumption in almost all experiments that the measured mobility of the biomolecule with its label is the same as that of the unlabeled molecule. However, this assumption is rarely tested due to a lack of suitable methods. In this work, a new technique to perform label-free diffusivity measurements is developed and used to measure the effect of the label for two common protein-lipid systems: 1) streptavidin (SA) coupled to a supported lipid bilayer (SLB) through biotinylated lipids and 2) the extracellular part of the T-cell adhesion protein CD2, coupled to an SLB through histidine tags to nickel-chelating lipids. A measurable (≈12%) decrease in diffusivity is found for both labeled proteins, even though the molecular mass of the label is almost 100 times smaller than those of the proteins (≈50 kDa). The results illustrate the importance of being able to study different biophysical properties of cell membranes and their mimics without relying on fluorescent labels, especially if fluorescent labeling is difficult or is expected to affect the nature of the intermolecular interactions being studied.
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- author
- Johansson, Björn ; Höök, Fredrik LU ; Klenerman, David and Jönsson, Peter LU
- publishing date
- 2014-02-24
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- CD2 Antigens, Chelating Agents, Diffusion, Hydrodynamics, Lipid Bilayers, Nickel, Streptavidin, Journal Article, Research Support, Non-U.S. Gov't
- in
- ChemPhysChem
- volume
- 15
- issue
- 3
- pages
- 6 pages
- publisher
- John Wiley & Sons Inc.
- external identifiers
-
- pmid:24402971
- scopus:84894263360
- ISSN
- 1439-7641
- DOI
- 10.1002/cphc.201301136
- language
- English
- LU publication?
- no
- id
- 0a56bb8c-0d3a-455f-995f-073665c74f16
- date added to LUP
- 2018-01-26 10:26:23
- date last changed
- 2024-01-14 14:15:12
@article{0a56bb8c-0d3a-455f-995f-073665c74f16,
abstract = {{<p>An important and characteristic property of a cell membrane is the lateral mobility of protein molecules in the lipid bilayer. This has conventionally been measured by labeling the molecules with fluorescent markers and monitoring their mobility by different fluorescence-based techniques. However, adding the label to the studied molecule may affect the system, so it is an assumption in almost all experiments that the measured mobility of the biomolecule with its label is the same as that of the unlabeled molecule. However, this assumption is rarely tested due to a lack of suitable methods. In this work, a new technique to perform label-free diffusivity measurements is developed and used to measure the effect of the label for two common protein-lipid systems: 1) streptavidin (SA) coupled to a supported lipid bilayer (SLB) through biotinylated lipids and 2) the extracellular part of the T-cell adhesion protein CD2, coupled to an SLB through histidine tags to nickel-chelating lipids. A measurable (≈12%) decrease in diffusivity is found for both labeled proteins, even though the molecular mass of the label is almost 100 times smaller than those of the proteins (≈50 kDa). The results illustrate the importance of being able to study different biophysical properties of cell membranes and their mimics without relying on fluorescent labels, especially if fluorescent labeling is difficult or is expected to affect the nature of the intermolecular interactions being studied.</p>}},
author = {{Johansson, Björn and Höök, Fredrik and Klenerman, David and Jönsson, Peter}},
issn = {{1439-7641}},
keywords = {{CD2 Antigens; Chelating Agents; Diffusion; Hydrodynamics; Lipid Bilayers; Nickel; Streptavidin; Journal Article; Research Support, Non-U.S. Gov't}},
language = {{eng}},
month = {{02}},
number = {{3}},
pages = {{91--486}},
publisher = {{John Wiley & Sons Inc.}},
series = {{ChemPhysChem}},
title = {{Label-free measurements of the diffusivity of molecules in lipid membranes}},
url = {{http://dx.doi.org/10.1002/cphc.201301136}},
doi = {{10.1002/cphc.201301136}},
volume = {{15}},
year = {{2014}},
}