3P19

Improved NADPH-dependent Blue Fluorescent Protein

3P19 の概要

• エントリーDOI: 10.2210/pdb3p19/pdb
• 分子名称: Putative blue fluorescent protein, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE (3 entities in total)
• 機能のキーワード: rossmann-fold, blue fluorescent protein, oxidoreductase
• 由来する生物種: Vibrio vulnificus
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 118546.59

構造登録者

Kao, T.H.,Chen, Y.,Pai, C.H.,Wang, A.H.J. (登録日: 2010-09-30, 公開日: 2011-07-20, 最終更新日: 2023-11-01)

主引用文献

Kao, T.H.,Chen, Y.,Pai, C.H.,Chang, M.C.,Wang, A.H.J.
Structure of a NADPH-dependent blue fluorescent protein revealed the unique role of Gly176 on the fluorescence enhancement.
J.Struct.Biol., 174:485-493, 2011

PubMed Abstract: A NADPH-dependent blue fluorescent protein from Vibrio vulnificus CKM-1 (BFPvv) emits blue fluorescence under UV-exposure. Previously, the BFPvvD7 mutant generated by directed evolution displayed a fourfold enhancement in fluorescent intensity. Herein, a further increase in fluorescence in the new BFPvvD8 mutant, with three additional mutations from BFPvvD7, was made. To understand the underlying mechanism of the increased fluorescent intensity of BFPvv, we solved the BFPvvD8-NADPH complex structure. Accompanied with lifetime detection, we proposed that the enhanced intensity is related to the conformational change caused by a glycine residue (Gly176) mutated to other non-glycine residues at a turn close to the NADPH binding site. We also observed the Förster resonance energy transfer (FRET) from our BFPvvD8 to each of the GFP-like fluorescent proteins, mTFP1 and EGFP, joined by an eight-residue linker between the N-terminal of BFPvvD8 and the C-terminal of GFPs. Taken together, with the newly solved BFPvvD8 structure, our results not only provide new considerations within the rational-based protein engineering of this NADPH-dependent BFP, but also suggest that BFPvvD8 could be a potential candidate in FRET-based biosensor techniques.

PubMed: 21397029
DOI: 10.1016/j.jsb.2011.02.010

実験手法

X-RAY DIFFRACTION (2.05 Å)