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Dilute Bicelles for Glycosyltransferase Studies, Novel Bicelles with Phosphatidylinositol
[Image: see text] Solution-state NMR can be used to study protein–lipid interactions, in particular, the effect that proteins have on lipids. One drawback is that only small assemblies can be studied, and therefore, fast-tumbling bicelles are commonly used. Bicelles contain a lipid bilayer that is s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358657/ https://www.ncbi.nlm.nih.gov/pubmed/35880265 http://dx.doi.org/10.1021/acs.jpcb.2c02327 |
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author | Patrick, Joan Alija, Mikel García Liebau, Jobst Pettersson, Pontus Metola, Ane Mäler, Lena |
author_facet | Patrick, Joan Alija, Mikel García Liebau, Jobst Pettersson, Pontus Metola, Ane Mäler, Lena |
author_sort | Patrick, Joan |
collection | PubMed |
description | [Image: see text] Solution-state NMR can be used to study protein–lipid interactions, in particular, the effect that proteins have on lipids. One drawback is that only small assemblies can be studied, and therefore, fast-tumbling bicelles are commonly used. Bicelles contain a lipid bilayer that is solubilized by detergents. A complication is that they are only stable at high concentrations, exceeding the CMC of the detergent. This issue has previously been addressed by introducing a detergent (Cyclosfos-6) with a substantially lower CMC. Here, we developed a set of bicelles using this detergent for studies of membrane-associated mycobacterial proteins, for example, PimA, a key enzyme for bacterial growth. To mimic the lipid composition of mycobacterial membranes, PI, PG, and PC lipids were used. Diffusion NMR was used to characterize the bicelles, and spin relaxation was used to measure the dynamic properties of the lipids. The results suggest that bicelles are formed, although they are smaller than “conventional” bicelles. Moreover, we studied the effect of MTSL-labeled PimA on bicelles containing PI and PC. The paramagnetic label was shown to have a shallow location in the bicelle, affecting the glycerol backbone of the lipids. We foresee that these bicelles will be useful for detailed studies of protein–lipid interactions. |
format | Online Article Text |
id | pubmed-9358657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93586572022-08-10 Dilute Bicelles for Glycosyltransferase Studies, Novel Bicelles with Phosphatidylinositol Patrick, Joan Alija, Mikel García Liebau, Jobst Pettersson, Pontus Metola, Ane Mäler, Lena J Phys Chem B [Image: see text] Solution-state NMR can be used to study protein–lipid interactions, in particular, the effect that proteins have on lipids. One drawback is that only small assemblies can be studied, and therefore, fast-tumbling bicelles are commonly used. Bicelles contain a lipid bilayer that is solubilized by detergents. A complication is that they are only stable at high concentrations, exceeding the CMC of the detergent. This issue has previously been addressed by introducing a detergent (Cyclosfos-6) with a substantially lower CMC. Here, we developed a set of bicelles using this detergent for studies of membrane-associated mycobacterial proteins, for example, PimA, a key enzyme for bacterial growth. To mimic the lipid composition of mycobacterial membranes, PI, PG, and PC lipids were used. Diffusion NMR was used to characterize the bicelles, and spin relaxation was used to measure the dynamic properties of the lipids. The results suggest that bicelles are formed, although they are smaller than “conventional” bicelles. Moreover, we studied the effect of MTSL-labeled PimA on bicelles containing PI and PC. The paramagnetic label was shown to have a shallow location in the bicelle, affecting the glycerol backbone of the lipids. We foresee that these bicelles will be useful for detailed studies of protein–lipid interactions. American Chemical Society 2022-07-26 2022-08-04 /pmc/articles/PMC9358657/ /pubmed/35880265 http://dx.doi.org/10.1021/acs.jpcb.2c02327 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/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 | Patrick, Joan Alija, Mikel García Liebau, Jobst Pettersson, Pontus Metola, Ane Mäler, Lena Dilute Bicelles for Glycosyltransferase Studies, Novel Bicelles with Phosphatidylinositol |
title | Dilute Bicelles
for Glycosyltransferase Studies, Novel
Bicelles with Phosphatidylinositol |
title_full | Dilute Bicelles
for Glycosyltransferase Studies, Novel
Bicelles with Phosphatidylinositol |
title_fullStr | Dilute Bicelles
for Glycosyltransferase Studies, Novel
Bicelles with Phosphatidylinositol |
title_full_unstemmed | Dilute Bicelles
for Glycosyltransferase Studies, Novel
Bicelles with Phosphatidylinositol |
title_short | Dilute Bicelles
for Glycosyltransferase Studies, Novel
Bicelles with Phosphatidylinositol |
title_sort | dilute bicelles
for glycosyltransferase studies, novel
bicelles with phosphatidylinositol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358657/ https://www.ncbi.nlm.nih.gov/pubmed/35880265 http://dx.doi.org/10.1021/acs.jpcb.2c02327 |
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