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One-step separation of myristoylated and nonmyristoylated retroviral matrix proteins

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F13%3A00399957" target="_blank" >RIV/61388963:_____/13:00399957 - isvavai.cz</a>

  • Alternative codes found

    RIV/60461373:22330/13:43895626 RIV/60461373:22810/13:43895626 RIV/60461373:22330/13:43897411 RIV/60461373:22810/13:43897411

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.pep.2013.09.003" target="_blank" >http://dx.doi.org/10.1016/j.pep.2013.09.003</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.pep.2013.09.003" target="_blank" >10.1016/j.pep.2013.09.003</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    One-step separation of myristoylated and nonmyristoylated retroviral matrix proteins

  • Original language description

    N-terminal myristoylation of retroviral matrix proteins is essential for the targeting of the Gag polyproteins to the plasma membrane. To investigate the effect of the myristoylation on the structure and membrane binding ability of the matrix proteins, it is necessary to prepare their myristoylated forms. We present purification of myristoylated matrix proteins of the mouse mammary tumor virus and murine leukemia virus, two morphogenetically distinct retroviruses. The proteins were expressed in Escherichia coli coexpressing a yeast N-myristoyltransferase. This E. coli expression system yielded a mixture of myristoylated and nonmyristoylated matrix proteins. We established efficient one-step metal affinity purification that enabled to obtain pure myristoylated matrix proteins suitable for structural and functional studies.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GA204%2F09%2F1388" target="_blank" >GA204/09/1388: Characterization of novel host cell protein interacting with protease of Mason-Pfizer monkey virus</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Protein Expression and Purification

  • ISSN

    1046-5928

  • e-ISSN

  • Volume of the periodical

    92

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

    94-99

  • UT code for WoS article

    000326257000014

  • EID of the result in the Scopus database