journal article·2020-04-14Open access

X-ray and Neutron Reflectivity Studies of Styrene-Maleic Acid Copolymer Interactions with Galactolipid-Containing Monolayers

Minh D. Phan, Olena I. Korotych, Nathan G. Brady, Madeline M. Davis, Sushil K. Satija, John F. Ankner, Barry D. Bruce

Langmuir· Volume 36· Issue 14

Abstract

Styrene-maleic acid (SMA) copolymers have recently gained attention for their ability to facilitate the detergent-free solubilization of membrane protein complexes and their native boundary lipids into polymer-encapsulated, nanosized lipid particles, referred to as SMALPs. However, the interfacial interactions between SMA and lipids, which dictate the mechanism, efficiency, and selectivity of lipid and membrane protein extraction, are barely understood. Our recent finding has shown that SMA 1440, a chemical derivative of the SMA family with a functionalized butoxyethanol group, was most active in galactolipid-rich membranes, as opposed to phospholipid membranes. In the present work, we have performed X-ray reflectometry (XRR) and neutron reflectometry (NR) on the lipid monolayers at the liquid–air interface followed by the SMA copolymer adsorption. XRR and Langmuir Π–A isotherms captured the fluidifying effect of galactolipids, which allowed SMA copolymers to infiltrate easily into the lipid membranes. NR results revealed the detailed structural arrangement of SMA 1440 copolymers within the membranes and highlighted the partition of butoxyethanol group into the lipid tail region. This work allows us to propose a possible mechanism for the membrane solubilization by SMA.
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Research context

OpenAlex topics: Lipid Membrane Structure and Behavior · Spectroscopy and Quantum Chemical Studies · Force Microscopy Techniques and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Large-Scale Structures Group, Neutron Scattering Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States

Department of Biochemistry, and Cellular, and Molecular Biology, University of Tennessee at Knoxville, Knoxville, Tennessee 37966, United States

Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, United States

Department of Microbiology, University of Tennessee at Knoxville, Knoxville, Tennessee 37966, United States

Funding

Oak Ridge National Laboratory · Office of Experimental Program to Stimulate Competitive Research · Division of Graduate Education · University of Tennessee, Knoxville · Gibson Family Foundation Inc. · Tennessee Plant Research Center, University of Tennessee, Knoxville

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