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Tailoring butyl methacrylate/methacrylic acid copolymers for the solubilization of membrane proteins: the influence of composition and molecular weight

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F22%3A00562629" target="_blank" >RIV/61389013:_____/22:00562629 - isvavai.cz</a>

  • Alternative codes found

    RIV/86652036:_____/22:00562629 RIV/68378050:_____/22:00562629 RIV/00216224:14740/22:00128767

  • Result on the web

    <a href="https://onlinelibrary.wiley.com/doi/10.1002/mabi.202200284" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1002/mabi.202200284</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/mabi.202200284" target="_blank" >10.1002/mabi.202200284</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Tailoring butyl methacrylate/methacrylic acid copolymers for the solubilization of membrane proteins: the influence of composition and molecular weight

  • Original language description

    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 × 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.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10404 - Polymer science

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Macromolecular Bioscience

  • ISSN

    1616-5187

  • e-ISSN

    1616-5195

  • Volume of the periodical

    22

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    7

  • Pages from-to

    2200284

  • UT code for WoS article

    000842344300001

  • EID of the result in the Scopus database

    2-s2.0-85136506500