TY - JOUR
T1 - FluoroCalins
T2 - engineered lipocalins with novel binding functions fused to a fluorescent protein for applications in biomolecular imaging and detection
AU - Eggenstein, Evelyn
AU - Richter, Antonia
AU - Skerra, Arne
N1 - Publisher Copyright:
© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: [email protected].
PY - 2019/12/31
Y1 - 2019/12/31
N2 - FluoroCalins represent novel bifunctional protein reagents derived from engineered lipocalins fused to a fluorescent reporter protein, here the enhanced green fluorescent protein (eGFP). We demonstrate the construction, facile bacterial production and broad applicability of FluoroCalins using two Anticalin® molecules directed against the tumor vasculature-associated extra domain B of fibronectin (ED-B) and the vascular endothelial growth factor receptor 3, a marker of tumor and lymphangiogenesis. FluoroCalins were prepared with two different spacers: (i) a short Ser3Ala linker and (ii) a long hydrophilic and conformationally unstructured PASylation® polypeptide comprising 200 Pro, Ala and Ser residues. These FluoroCalins were applied for direct target quantification in enzyme-linked immunosorbent assay as well as target detection by flow cytometry and fluorescence microscopy of live and fixed cells, respectively, demonstrating high specificity and signal-to-noise ratio. Hence, FluoroCalins offer a promising alternative to antibody-based reagents for state of the art fluorescent in vitro detection and biomolecular imaging.
AB - FluoroCalins represent novel bifunctional protein reagents derived from engineered lipocalins fused to a fluorescent reporter protein, here the enhanced green fluorescent protein (eGFP). We demonstrate the construction, facile bacterial production and broad applicability of FluoroCalins using two Anticalin® molecules directed against the tumor vasculature-associated extra domain B of fibronectin (ED-B) and the vascular endothelial growth factor receptor 3, a marker of tumor and lymphangiogenesis. FluoroCalins were prepared with two different spacers: (i) a short Ser3Ala linker and (ii) a long hydrophilic and conformationally unstructured PASylation® polypeptide comprising 200 Pro, Ala and Ser residues. These FluoroCalins were applied for direct target quantification in enzyme-linked immunosorbent assay as well as target detection by flow cytometry and fluorescence microscopy of live and fixed cells, respectively, demonstrating high specificity and signal-to-noise ratio. Hence, FluoroCalins offer a promising alternative to antibody-based reagents for state of the art fluorescent in vitro detection and biomolecular imaging.
KW - ED-B
KW - PASylation
KW - VEGFR-3
KW - anticalin
KW - eGFP
UR - http://www.scopus.com/inward/record.url?scp=85080849951&partnerID=8YFLogxK
U2 - 10.1093/protein/gzz047
DO - 10.1093/protein/gzz047
M3 - Article
C2 - 31927584
AN - SCOPUS:85080849951
SN - 1741-0126
VL - 32
SP - 289
EP - 296
JO - Protein Engineering, Design and Selection
JF - Protein Engineering, Design and Selection
IS - 6
ER -