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Resolution: standard / high Figure 1.
Proteomic analysis identifies hnRNP L as a major nuclear Sam68-interacting protein. (A) LNCaP cell nuclear extracts were subjected to immunoprecipitation (IP) using
anti-Sam68 rabbit antisera. IP was carried out in the presence or absence (+/-) of
antisera to Sam68, with or without (+/-) Dynabeads Protein A, and either with or without
(+/-) prior cross-linking of the antisera to the Dynabeads Protein A. Immunoprecipitates
were resolved by SDS-PAGE, and six bands were excised from the Coomassie-stained gel
for identification by peptide mass fingerprinting, of which 4 were positively identified.
(B to E) MASCOT search results for Sam68-interacting proteins: Swiss-Prot entry names
KHDR1_HUMAN (B: Sam68), ROA1_HUMAN (C: hnRNP A1), ROA2_HUMAN (C: hnRNP A2/B1), HNRPG_HUMAN
(D: hnRNP G), and HNRPL_HUMAN (E: hnRNP L). Histograms show the MOWSE score distributions
for identified peptides, with matched peptide sequences shown in bold red. The band
corresponding to histogram (C) contained a mixture of peptides matching to Swiss-Prot
entry names ROA1_HUMAN and ROA2_HUMAN.
Rajan et al. BMC Cell Biology 2009 10:82 doi:10.1186/1471-2121-10-82 |