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PMID: 22956099 Published · ppublish English Journal Article

Immunoisolation of protein complexes from Xenopus.

Methods in molecular biology (Clifton, N.J.) ·Vol. 917 ·2012-00-00 ·Pages 369-90

Conlon FL, Miteva Y, Kaltenbrun E, Waldron L, Greco TM, Cristea IM

Abstract

The immunoaffinity isolation of protein complexes is an essential technique for the purification and -concentration of protein complexes from cells and tissues. In this chapter we present the methodologies for the purification of proteins and protein complexes from Xenopus laevis and Xenopus tropicalis. Specific to this protocol are the techniques for the cryolysis of Xenopus cells and tissues, a procedure that limits contamination from yolk proteins while preserving endogenous protein complexes, the methodologies for immunoaffinity purification of proteins using magnetic beads, and the protocols for western blot analysis. In addition, the procedures in this chapter can be extended to use with proteomic analysis of protein complexes as presented in the following chapter.

MeSH Terms
Animals Antibodies, Immobilized/chemistry,immunology Antibody Affinity Blotting, Western Buffers Electrophoresis, Polyacrylamide Gel Embryo, Nonmammalian/metabolism Immunoprecipitation/methods Magnets/chemistry Microspheres Multiprotein Complexes/immunology,isolation & purification Xenopus Proteins/immunology,isolation & purification Xenopus laevis/metabolism
Chemicals
Antibodies, Immobilized Buffers Multiprotein Complexes Xenopus Proteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Conlon Frank L
Department of Genetics, University of North Carolina, Chapel Hill, NC, USA. frank_conlon@med.unc.edu
Miteva Yana
Kaltenbrun Erin
Waldron Lauren
Greco Todd M
Cristea Ileana M
References (7)
7 references, click to expand
  1. Proteomic studies of a single CNS synapse type: the parallel fiber/purkinje cell synapse.
    PLoS Biol. 2009 Apr 14;7(4):e83 PMID: 19402746
  2. Nuclear import of histone deacetylase 5 by requisite nuclear localization signal phosphorylation.
    Mol Cell Proteomics. 2011 Feb;10(2):M110.004317 PMID: 21081666
  3. The response regulator SprE (RssB) is required for maintaining poly(A) polymerase I-degradosome association during stationary phase.
    J Bacteriol. 2010 Jul;192(14):3713-21 PMID: 20472786
  4. Fluorescent proteins as proteomic probes.
    Mol Cell Proteomics. 2005 Dec;4(12):1933-41 PMID: 16155292
  5. Distinct factors control histone variant H3.3 localization at specific genomic regions.
    Cell. 2010 Mar 5;140(5):678-91 PMID: 20211137
  6. Tracking and elucidating alphavirus-host protein interactions.
    J Biol Chem. 2006 Oct 6;281(40):30269-78 PMID: 16895903
  7. A targeted spatial-temporal proteomics approach implicates multiple cellular trafficking pathways in human cytomegalovirus virion maturation.
    Mol Cell Proteomics. 2010 May;9(5):851-60 PMID: 20023299
Article Info
Journal
Methods in molecular biology (Clifton, N.J.)
Abbr.
Methods Mol Biol
ISSN
1940-6029
Published
2012-00-00
Pages
369-90
Language
English
Region
United States
NLM ID
9214969
PMCID
PMC3640821
Subset
IM
Grants
NIDCR NIH HHS · R01 DE018825 · United States
NICHD NIH HHS · R21 HD073044 · United States
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