Ab initio reconstruction of small angle scattering data for membrane proteins in copolymer nanodiscs
Morrison, Kerrie A. ; Doekhie, Aswin ; Neville, George M. ; Price, Gareth J. ; Whitley, Paul ; Doutch, James and Edler, Karen J. LU
(2022)
In BBA Advances
2.
- Abstract
Background: Small angle scattering techniques are beginning to be more widely utilised for structural analysis of biological systems. However, applying these techniques to study membrane proteins still remains problematic, due to sample preparation requirements and analysis of the resulting data. The development of styrene-maleic acid co-polymers (SMA) to extract membrane proteins into nanodiscs for further study provides a suitable environment for structural analysis.
Methods: We use small angle neutron scattering (SANS) with three different contrasts to determine structural information for two different polymer nanodisc-incorporated proteins, Outer membrane protein F (OmpF) and gramicidin. Ab initio modelling was applied... (More)
Background: Small angle scattering techniques are beginning to be more widely utilised for structural analysis of biological systems. However, applying these techniques to study membrane proteins still remains problematic, due to sample preparation requirements and analysis of the resulting data. The development of styrene-maleic acid co-polymers (SMA) to extract membrane proteins into nanodiscs for further study provides a suitable environment for structural analysis.
Methods: We use small angle neutron scattering (SANS) with three different contrasts to determine structural information for two different polymer nanodisc-incorporated proteins, Outer membrane protein F (OmpF) and gramicidin. Ab initio modelling was applied to generate protein/lipid structures from the SANS data. Other complementary structural methodologies, such as DLS, CD and TEM were compared alongside this data with known protein crystal structures.
Results: A single-phase model was constructed for gramicidin-containing nanodiscs, which showed dimer formation in the centre of the nanodisc. For OmpF-nanodiscs we were able to construct a multi-phase model, providing structural information on the protein/lipid and polymer components of the sample.
Conclusions: Polymer-nanodiscs can provide a suitable platform to investigate certain membrane proteins using SANS, alongside other structural methodologies. However, differences between the published crystal structure and OmpF-nanodiscs were observed, suggesting the nanodisc structure could be altering the folding of the protein.
General significance: Small angle scattering techniques can provide structural information on the protein and polymer nanodisc without requiring crystallisation of the protein. Additional complementary techniques, such as ab initio modelling, can generate alternative models both the protein and nanodisc system.
(Less)
- author
- Morrison, Kerrie A.
; Doekhie, Aswin
; Neville, George M.
; Price, Gareth J.
; Whitley, Paul
; Doutch, James
and Edler, Karen J.
LU
- publishing date
- 2022-01
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Ab initio, MONSA, Nanodisc, Outer membrane protein F, Small angle neutron scattering, SMALP
- in
- BBA Advances
- volume
- 2
- article number
- 100033
- pages
- 11 pages
- publisher
- Elsevier
- external identifiers
-
- pmid:37082608
- scopus:85123989583
- DOI
- 10.1016/j.bbadva.2021.100033
- language
- English
- LU publication?
- no
- additional info
- Publisher Copyright: © 2021
- id
- efc02cc1-4229-4217-9110-912606193016
- date added to LUP
- 2022-07-12 14:01:06
- date last changed
- 2024-04-16 08:29:15
@article{efc02cc1-4229-4217-9110-912606193016,
abstract = {{<p>Background: Small angle scattering techniques are beginning to be more widely utilised for structural analysis of biological systems. However, applying these techniques to study membrane proteins still remains problematic, due to sample preparation requirements and analysis of the resulting data. The development of styrene-maleic acid co-polymers (SMA) to extract membrane proteins into nanodiscs for further study provides a suitable environment for structural analysis. <br/></p><p>Methods: We use small angle neutron scattering (SANS) with three different contrasts to determine structural information for two different polymer nanodisc-incorporated proteins, Outer membrane protein F (OmpF) and gramicidin. Ab initio modelling was applied to generate protein/lipid structures from the SANS data. Other complementary structural methodologies, such as DLS, CD and TEM were compared alongside this data with known protein crystal structures. <br/></p><p>Results: A single-phase model was constructed for gramicidin-containing nanodiscs, which showed dimer formation in the centre of the nanodisc. For OmpF-nanodiscs we were able to construct a multi-phase model, providing structural information on the protein/lipid and polymer components of the sample. <br/></p><p>Conclusions: Polymer-nanodiscs can provide a suitable platform to investigate certain membrane proteins using SANS, alongside other structural methodologies. However, differences between the published crystal structure and OmpF-nanodiscs were observed, suggesting the nanodisc structure could be altering the folding of the protein. <br/></p><p>General significance: Small angle scattering techniques can provide structural information on the protein and polymer nanodisc without requiring crystallisation of the protein. Additional complementary techniques, such as ab initio modelling, can generate alternative models both the protein and nanodisc system.</p>}},
author = {{Morrison, Kerrie A. and Doekhie, Aswin and Neville, George M. and Price, Gareth J. and Whitley, Paul and Doutch, James and Edler, Karen J.}},
keywords = {{Ab initio; MONSA; Nanodisc; Outer membrane protein F; Small angle neutron scattering; SMALP}},
language = {{eng}},
publisher = {{Elsevier}},
series = {{BBA Advances}},
title = {{<i>Ab initio</i> reconstruction of small angle scattering data for membrane proteins in copolymer nanodiscs}},
url = {{http://dx.doi.org/10.1016/j.bbadva.2021.100033}},
doi = {{10.1016/j.bbadva.2021.100033}},
volume = {{2}},
year = {{2022}},
}