How to minimize dye-induced perturbations while studying biomembrane structure and dynamics: PEG linkers as a rational alternative
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
091911
Wellcome Trust - United Kingdom
MC_UU_00008/9
Medical Research Council - United Kingdom
MC_UU_12010/9
Medical Research Council - United Kingdom
MR/K01577X/1
Medical Research Council - United Kingdom
PubMed
30028957
DOI
10.1016/j.bbamem.2018.07.003
PII: S0005-2736(18)30198-6
Knihovny.cz E-zdroje
- Klíčová slova
- Atomistic simulation, Fluorescent probe, Lipid membrane, Molecular dynamics simulation, PEG linker, Super-resolution microscopy,
- MeSH
- difuze MeSH
- fluorescenční barviva chemie metabolismus MeSH
- fosfatidylcholiny chemie MeSH
- lipidové dvojvrstvy chemie metabolismus MeSH
- polyethylenglykoly chemie MeSH
- simulace molekulární dynamiky MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 1,2-oleoylphosphatidylcholine MeSH Prohlížeč
- fluorescenční barviva MeSH
- fosfatidylcholiny MeSH
- lipidové dvojvrstvy MeSH
- polyethylenglykoly MeSH
Organic dye-tagged lipid analogs are essential for many fluorescence-based investigations of complex membrane structures, especially when using advanced microscopy approaches. However, lipid analogs may interfere with membrane structure and dynamics, and it is not obvious that the properties of lipid analogs would match those of non-labeled host lipids. In this work, we bridged atomistic simulations with super-resolution imaging experiments and biomimetic membranes to assess the performance of commonly used sphingomyelin-based lipid analogs. The objective was to compare, on equal footing, the relative strengths and weaknesses of acyl chain labeling, headgroup labeling, and labeling based on poly-ethyl-glycol (PEG) linkers in determining biomembrane properties. We observed that the most appropriate strategy to minimize dye-induced membrane perturbations and to allow consideration of Brownian-like diffusion in liquid-ordered membrane environments is to decouple the dye from a membrane by a PEG linker attached to a lipid headgroup. Yet, while the use of PEG linkers may sound a rational and even an obvious approach to explore membrane dynamics, the results also suggest that the dyes exploiting PEG linkers interfere with molecular interactions and their dynamics. Overall, the results highlight the great care needed when using fluorescent lipid analogs, in particular accurate controls.
Department of Physics University of Helsinki P O Box 64 FI 00014 Helsinki Finland
Max Planck Institute of Molecular Cell Biology and Genetics Pfotenhauerstr 108 01307 Dresden Germany
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