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. 2014 Nov 21;3(12):1252–1261. doi: 10.1242/bio.201410041

Fig. 2. Binding of anti-GFP-DARPin-Ruby2 fusions to GFP in HeLa cells.

Fig. 2.

Shown are HeLa cells transiently overexpressing a DARPin-mRuby2 fusion protein (A–G) (H is an mRuby2-nanobody fusion) together with a GFP version tethered to the plasma membrane (GFP-CVIM, A′–H′). Overlap of fluorescent signal indicates binding of the respective anti-GFP-DARPin-mRuby2 fusion to GFP-CVIM, indicated by the yellow fluorescent signal at the plasma membrane. (A–A″) As expected, the anti-mCherry DARPin 2m22-mRuby2 fusion protein, which does not recognize GFP, is not recruited to the plasma membrane. (B–B″) 3G86.32-mRuby2, (C–C″) 3G168-mRuby2, (D–D″) 3G124-mRuby2 as well as (E–E″) 3G86.1-mRuby2 fusion proteins localize to the plasma membrane where they interact with GFP-CVIM. On the other hand, low affinity (F–F″) 3G61-mRuby2 and (G–G″) 3G146-mRuby2 fusion proteins localize to the cytoplasm and nucleus, indicating that they cannot interact sufficiently with GFP-CVIM anchored in the plasma membrane. (H–H″) Positive control mRuby2-VHH-GFP4 fusion protein localizes to the plasma membrane. Unprimed letters, mRuby2 channel; primed letters, GFP channel; double primed letters, overlay. Scale bars are 20 µm.