In spite of the numerous experimental and theoretical studies on green fluorescent protein and its modifications, there is still no definitive answer to the central question: why such systems exhibit enhanced fluorescence. Based upon detailed quantum-chemical estimations, we advocate the following hypothesis. In the green fluorescent protein ground electronic state, the protein surrounding strains the chromophore with respect to its native intramolecular conformational preference in vacuo or in solution. Absorbing a photon of the proper wavelength not only causes a joint proton–electron transfer in and around the chromophore, but also increases the intrinsic strain of the latter. Since conformational relaxation of such a structure will not ...
We demonstrate by using low-temperature high-resolution spectroscopy that red-shifted mutants of gre...
The nature of the coupling of the photoexcited chromophore with the environment in a prototypical sy...
We demonstrate by using low-temperature high-resolution spectroscopy that red-shifted mutants of gre...
The green fluorescent protein and its designed variants fluoresce efficiently. Because the isolated ...
The fluorescence emission from green fluorescent protein (GFP) is known to be heavily influenced by ...
Abstract: Two ground-state protonation forms causing different absorption peaks of the green fluores...
AbstractThe three amino acids S65, T203, and E222 crucially determine the photophysical behavior of ...
Green fluorescent protein (GFP) and GFP-like fluorescent proteins owe their photophysical properties...
Green fluorescent protein (GFP), together with its family of variants, is the most widely used fluor...
Ab initio CASPT2//CASSCF relaxation path computations are employed to determine the intrinsic (e.g.,...
Solvation plays an important role in the function of fluorescent proteins. Many of these proteins co...
AbstractThe photophysical properties of synthetic compounds derived from the imidazolidinone chromop...
3Photoinitiated phenomena play a crucial role in many living organisms. Plants, algae, and bacteria ...
Solvation plays an important role in the function of fluorescent proteins. Many of these proteins co...
The nature of the coupling of the photoexcited chromophore with the environment in a prototypical sy...
We demonstrate by using low-temperature high-resolution spectroscopy that red-shifted mutants of gre...
The nature of the coupling of the photoexcited chromophore with the environment in a prototypical sy...
We demonstrate by using low-temperature high-resolution spectroscopy that red-shifted mutants of gre...
The green fluorescent protein and its designed variants fluoresce efficiently. Because the isolated ...
The fluorescence emission from green fluorescent protein (GFP) is known to be heavily influenced by ...
Abstract: Two ground-state protonation forms causing different absorption peaks of the green fluores...
AbstractThe three amino acids S65, T203, and E222 crucially determine the photophysical behavior of ...
Green fluorescent protein (GFP) and GFP-like fluorescent proteins owe their photophysical properties...
Green fluorescent protein (GFP), together with its family of variants, is the most widely used fluor...
Ab initio CASPT2//CASSCF relaxation path computations are employed to determine the intrinsic (e.g.,...
Solvation plays an important role in the function of fluorescent proteins. Many of these proteins co...
AbstractThe photophysical properties of synthetic compounds derived from the imidazolidinone chromop...
3Photoinitiated phenomena play a crucial role in many living organisms. Plants, algae, and bacteria ...
Solvation plays an important role in the function of fluorescent proteins. Many of these proteins co...
The nature of the coupling of the photoexcited chromophore with the environment in a prototypical sy...
We demonstrate by using low-temperature high-resolution spectroscopy that red-shifted mutants of gre...
The nature of the coupling of the photoexcited chromophore with the environment in a prototypical sy...
We demonstrate by using low-temperature high-resolution spectroscopy that red-shifted mutants of gre...