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. Author manuscript; available in PMC: 2023 Apr 1.
Published in final edited form as: Small. 2022 May 26;19(13):e2202104. doi: 10.1002/smll.202202104

Figure 1:

Figure 1:

Schematic illustration of genetic constructs (top panels) and their corresponding protein variants (bottom panels) used in this work (A-F). A) sCatch-GFP: Split sfCherry1–10 fused to SpyCatcher and sfGFP without a transmembrane domain. B) sTag-BFP: Split sfCherry11 fused to SpyTag and TagBFP without a transmembrane domain. C) InterCatch: Split sfCherry1–10 fused to SpyCatcher and single-pass transmembrane domain of transferrin receptor (TfR). D) InterTag: Split sfCherry11 fused to SpyTag and single-pass transmembrane domain of platelet derived growth factor receptor (PDGFR). E) InterCatch-GFP: Split sfCherry1–10 fused to SpyCatcher, sfGFP and TfR transmembrane domain. F) InterTag-BFP: Split sfCherry11 fused to SpyTag, TagBFP and PDGFR transmembrane domain. (G) SpyTag/SpyCatcher assisted reconstitution of fluorescent sfCherry using transmembrane and soluble versions of InterSpy.