6LR7

Crystal structure of GFPuv complexed with the nanobody LaG16 at 1.67 Angstron resolution

6LR7 の概要

• エントリーDOI: 10.2210/pdb6lr7/pdb
• 分子名称: Green fluorescent protein, Nanobody LaG16 (3 entities in total)
• 機能のキーワード: complex, nanobody, green fluorescent protein, gfpuv, lag16, fluorescent protein
• 由来する生物種: Aequorea victoria; 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 41578.66

構造登録者

Zhang, Z.Y.,Ding, Y.,Hattori, M. (登録日: 2020-01-15, 公開日: 2020-04-29, 最終更新日: 2024-11-06)

主引用文献

Zhang, Z.,Wang, Y.,Ding, Y.,Hattori, M.
Structure-based engineering of anti-GFP nanobody tandems as ultra-high-affinity reagents for purification.
Sci Rep, 10:6239-6239, 2020

PubMed Abstract: 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) linker had the highest affinity with a K of 0.5 nM. The GFP-enhancer-(GGGGS)-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.

PubMed: 32277083
DOI: 10.1038/s41598-020-62606-7

実験手法

X-RAY DIFFRACTION (1.67 Å)