Exploiting neutron scattering contrast variation in biological membrane studies.
Jeremy H LakeyNicolò ParaciniLuke A CliftonPublished in: Biophysics reviews (2022)
Biological membranes composed of lipids and proteins are central for the function of all cells and individual components, such as proteins, that are readily studied by a range of structural approaches, including x-ray crystallography and cryo-electron microscopy. However, the study of complex molecular mixtures within the biological membrane structure and dynamics requires techniques that can study nanometer thick molecular bilayers in an aqueous environment at ambient temperature and pressure. Neutron methods, including scattering and spectroscopic approaches, are useful since they can measure structure and dynamics while also being able to penetrate sample holders and cuvettes. The structural approaches, such as small angle neutron scattering and neutron reflectometry, detect scattering caused by the difference in neutron contrast (scattering length) between different molecular components such as lipids or proteins. Usually, the bigger the contrast, the clearer the structural data, and this review uses examples from our research to illustrate how contrast can be increased to allow the structures of individual membrane components to be resolved. Most often this relies upon the use of deuterium in place of hydrogen, but we also discuss the use of magnetic contrast and other elements with useful scattering length values.
Keyphrases
- magnetic resonance
- electron microscopy
- high resolution
- contrast enhanced
- induced apoptosis
- magnetic resonance imaging
- ionic liquid
- air pollution
- monte carlo
- molecular docking
- single molecule
- computed tomography
- mass spectrometry
- particulate matter
- endoplasmic reticulum stress
- machine learning
- big data
- artificial intelligence
- molecularly imprinted