TY - JOUR
T1 - Analysis of protein ubiquitination.
AU - Laney, Jeffrey D.
AU - Hochstrasser, Mark
PY - 2002/11
Y1 - 2002/11
N2 - Attachment of ubiquitin (Ub) to a protein requires a complex of enzymes that recognize the substrate and promote Ub transfer. Sequence motifs present in these enzymes may indicate that other uncharacterized proteins containing these motifs have a biochemical function of Ub-protein ligation, and several in vitro methods are described in this unit for determining if a protein has Ub-transferring activity. They include psmunoblotting of psmunoprecipitated proteins, affinity purification using His-tagged ubiquitin, assaying for auto-ubiquitination of E3, and assaying ubiquitination of a model substrate protein. These methods are suitable for a variety of eukaryotic cells, but techniques are specifically described for use with yeast and mammalian cells.
AB - Attachment of ubiquitin (Ub) to a protein requires a complex of enzymes that recognize the substrate and promote Ub transfer. Sequence motifs present in these enzymes may indicate that other uncharacterized proteins containing these motifs have a biochemical function of Ub-protein ligation, and several in vitro methods are described in this unit for determining if a protein has Ub-transferring activity. They include psmunoblotting of psmunoprecipitated proteins, affinity purification using His-tagged ubiquitin, assaying for auto-ubiquitination of E3, and assaying ubiquitination of a model substrate protein. These methods are suitable for a variety of eukaryotic cells, but techniques are specifically described for use with yeast and mammalian cells.
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U2 - 10.1002/0471140864.ps1405s29
DO - 10.1002/0471140864.ps1405s29
M3 - Article
C2 - 18429222
AN - SCOPUS:45549096796
SN - 1934-3655
VL - Chapter 14
SP - Unit 14.5
JO - Current protocols in protein science / editorial board, John E. Coligan ... [et al.]
JF - Current protocols in protein science / editorial board, John E. Coligan ... [et al.]
ER -