JANATA, Miroslav, Eva CADOVA, Pavla ANGELISOVA, Tatsiana CHARNAVETS, Vaclav HOREJSI and Vladimir RAUS. Tailoring Butyl Methacrylate/Methacrylic Acid Copolymers for the Solubilization of Membrane Proteins: The Influence of Composition and Molecular Weight. Macromolecular Bioscience. WEINHEIM: Wiley-VCH, 2022, vol. 22, No 10, p. 2200284-2200290. ISSN 1616-5187. Available from: https://dx.doi.org/10.1002/mabi.202200284.
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Basic information
Original name Tailoring Butyl Methacrylate/Methacrylic Acid Copolymers for the Solubilization of Membrane Proteins: The Influence of Composition and Molecular Weight
Authors JANATA, Miroslav, Eva CADOVA, Pavla ANGELISOVA, Tatsiana CHARNAVETS, Vaclav HOREJSI and Vladimir RAUS.
Edition Macromolecular Bioscience, WEINHEIM, Wiley-VCH, 2022, 1616-5187.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher Germany
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.600
RIV identification code RIV/00216224:14740/22:00128767
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1002/mabi.202200284
UT WoS 000842344300001
Keywords in English amphiphilic copolymers; isolation; membrane proteins; screening; solubilization
Tags ne MU, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 28/2/2023 15:33.
Abstract
Low-molecular weight (MW) amphiphilic copolymers have been recently introduced as a powerful tool for the detergent-free isolation of cell membrane proteins. Herein, a screening approach is used to identify a new copolymer type for this application. Via a two-step ATRP/acidolysis procedure, a 3 x 3 matrix of well-defined poly[(butyl methacrylate)-co-(methacrylic acid)] copolymers (denoted BMAA) differing in their MW and ratio of hydrophobic (BMA) and hydrophilic (MAA) units is prepared. Subsequently, using the biologically relevant model (T-cell line Jurkat), two compositions of BMAA copolymers are identified that solubilize cell membranes to an extent comparable to the industry standard, styrene-maleic acid copolymer (SMA), while avoiding the potentially problematic phenyl groups. Surprisingly, while only the lowest-MW variant of the BMA/MAA 2:1 composition is effective, all the copolymers of the BMA/MAA 1:1 composition are found to solubilize the model membranes, including the high-MW variant (MW of 14 000). Importantly, the density gradient ultracentrifugation/sodium dodecyl sulfate-polyacrylamide gel electrophoresis/Western blotting experiments reveal that the BMA/MAA 1:1 copolymers disintegrate the Jurkat membranes differently than SMA, as demonstrated by the different distribution patterns of two tested membrane protein markers. This makes the BMAA copolymers a useful tool for studies on membrane microdomains differing in their composition and resistance to membrane-disintegrating polymers.
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