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. 2012 Feb;217-884(2):256–264. doi: 10.1016/j.imbio.2011.07.021

Fig. 5.

Fig. 5

Comparison of thioester protein functionalization for biotin–PEG4–hydrazide and biotin–PEG3–aminoxy. (A) Chemical structures of biotin–PEG4–hydrazide (top) and biotin–PEG3–aminoxy (bottom). (B) PEG-plasma was incubated with biotin–PEG4–hydrazide, biotin–PEG3–aminoxy. Biotinylated proteins were captured with SA-resin, eluted by boiling in SDS loading buffer and visualised by 6% SDS-PAGE and Coomassie staining. Total protein present in reaction mix pre-SA capture (left 3 lanes) is shown beside the pull-down proteins (right three lanes).