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Structure-based engineering of anti-GFP nanobody tandems as ultra-high-affinity reagents for purification
by
Wang, Yao
, Hattori, Motoyuki
, Ding, Yu
, Zhang, Ziyue
in
101/1
/ 631/1647/2230/2233
/ 631/45/269
/ 631/535/1266
/ 631/57/2267
/ 82
/ 9/10
/ Affinity
/ Affinity Labels - metabolism
/ Amino Acid Sequence - genetics
/ Binders
/ Binding sites
/ Binding Sites - genetics
/ Biological research
/ Chromatography, Affinity
/ Crystal structure
/ Crystallography, X-Ray
/ Green fluorescent protein
/ Green Fluorescent Proteins - antagonists & inhibitors
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Green Fluorescent Proteins - ultrastructure
/ Humanities and Social Sciences
/ Kinases
/ Membrane proteins
/ multidisciplinary
/ Nanobodies
/ Protein Engineering - methods
/ Protein purification
/ Reagents
/ Receptors, Purinergic P2X4
/ Science
/ Science (multidisciplinary)
/ Single-Domain Antibodies - genetics
/ Single-Domain Antibodies - metabolism
/ Single-Domain Antibodies - ultrastructure
/ Structure-Activity Relationship
/ Zebrafish Proteins - genetics
/ Zebrafish Proteins - isolation & purification
2020
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Structure-based engineering of anti-GFP nanobody tandems as ultra-high-affinity reagents for purification
by
Wang, Yao
, Hattori, Motoyuki
, Ding, Yu
, Zhang, Ziyue
in
101/1
/ 631/1647/2230/2233
/ 631/45/269
/ 631/535/1266
/ 631/57/2267
/ 82
/ 9/10
/ Affinity
/ Affinity Labels - metabolism
/ Amino Acid Sequence - genetics
/ Binders
/ Binding sites
/ Binding Sites - genetics
/ Biological research
/ Chromatography, Affinity
/ Crystal structure
/ Crystallography, X-Ray
/ Green fluorescent protein
/ Green Fluorescent Proteins - antagonists & inhibitors
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Green Fluorescent Proteins - ultrastructure
/ Humanities and Social Sciences
/ Kinases
/ Membrane proteins
/ multidisciplinary
/ Nanobodies
/ Protein Engineering - methods
/ Protein purification
/ Reagents
/ Receptors, Purinergic P2X4
/ Science
/ Science (multidisciplinary)
/ Single-Domain Antibodies - genetics
/ Single-Domain Antibodies - metabolism
/ Single-Domain Antibodies - ultrastructure
/ Structure-Activity Relationship
/ Zebrafish Proteins - genetics
/ Zebrafish Proteins - isolation & purification
2020
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Structure-based engineering of anti-GFP nanobody tandems as ultra-high-affinity reagents for purification
by
Wang, Yao
, Hattori, Motoyuki
, Ding, Yu
, Zhang, Ziyue
in
101/1
/ 631/1647/2230/2233
/ 631/45/269
/ 631/535/1266
/ 631/57/2267
/ 82
/ 9/10
/ Affinity
/ Affinity Labels - metabolism
/ Amino Acid Sequence - genetics
/ Binders
/ Binding sites
/ Binding Sites - genetics
/ Biological research
/ Chromatography, Affinity
/ Crystal structure
/ Crystallography, X-Ray
/ Green fluorescent protein
/ Green Fluorescent Proteins - antagonists & inhibitors
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Green Fluorescent Proteins - ultrastructure
/ Humanities and Social Sciences
/ Kinases
/ Membrane proteins
/ multidisciplinary
/ Nanobodies
/ Protein Engineering - methods
/ Protein purification
/ Reagents
/ Receptors, Purinergic P2X4
/ Science
/ Science (multidisciplinary)
/ Single-Domain Antibodies - genetics
/ Single-Domain Antibodies - metabolism
/ Single-Domain Antibodies - ultrastructure
/ Structure-Activity Relationship
/ Zebrafish Proteins - genetics
/ Zebrafish Proteins - isolation & purification
2020
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Structure-based engineering of anti-GFP nanobody tandems as ultra-high-affinity reagents for purification
Journal Article
Structure-based engineering of anti-GFP nanobody tandems as ultra-high-affinity reagents for purification
2020
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Overview
Green fluorescent proteins (GFPs) are widely used in biological research. Although GFP can be visualized easily, its precise manipulation through binding partners is still burdensome because of the limited availability of high-affinity binding partners and related structural information. Here, we report the crystal structure of GFPuv in complex with the anti-GFP nanobody LaG16 at 1.67 Å resolution, revealing the details of the binding between GFPuv and LaG16. The LaG16 binding site was on the opposite side of the GFP β-barrel from the binding site of the GFP-enhancer, another anti-GFP nanobody, indicating that the GFP-enhancer and LaG16 can bind to GFP together. Thus, we further designed 3 linkers of different lengths to fuse LaG16 and GFP-enhancer together, and the GFP binding of the three constructs was further tested by ITC. The construct with the (GGGGS)
4
linker had the highest affinity with a K
D
of 0.5 nM. The GFP-enhancer-(GGGGS)
4
-LaG16 chimeric nanobody was further covalently linked to NHS-activated agarose and then used in the purification of a GFP-tagged membrane protein, GFP-tagged zebrafish P2X4, resulting in higher yield than purification with the GFP-enhancer nanobody alone. This work provides a proof of concept for the design of ultra-high-affinity binders of target proteins through dimerized nanobody chimaeras, and this strategy may also be applied to link interesting target protein nanobodies without overlapping binding surfaces.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ 82
/ 9/10
/ Affinity
/ Affinity Labels - metabolism
/ Amino Acid Sequence - genetics
/ Binders
/ Green Fluorescent Proteins - antagonists & inhibitors
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Green Fluorescent Proteins - ultrastructure
/ Humanities and Social Sciences
/ Kinases
/ Protein Engineering - methods
/ Reagents
/ Science
/ Single-Domain Antibodies - genetics
/ Single-Domain Antibodies - metabolism
/ Single-Domain Antibodies - ultrastructure
/ Structure-Activity Relationship
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