AbstractPhotoactive yellow protein (PYP) is a novel type of photoreceptor containing a thiol ester-linked p-coumarate anion chromophore. Photoexcitation of PYP triggers a photocycle which involves at least two intermediates: an early red-shifted state and a long-lived blue-shifted state (pB). At pH values below 3 PYP is reversibly converted into a stable blue-shifted state (pBdark). Here we quantify the transition from pG to pBdark at reduced pH as a two-state transition with an apparent pK of 2.8 and a steepness of 1.35 and report that the formation of pBdark is also induced by increased pressure (midpoint ∼1250atm at pH 2.7). The last step in the photocycle of PYP, from pB back to pG, is strongly decelerated by acidification. By global an...
The bacterial photoreceptor protein photoactive yellow protein (PYP) covalently binds the chromophor...
AbstractAs a bacterial blue light sensor the photoactive yellow protein (PYP) undergoes conformation...
AbstractVisualizing the three-dimensional structures of a protein during its biological activity is ...
Photoactive yellow protein (PYP) is a novel type of photoreceptor containing a thiol ester-linked p-...
AbstractPhotoactive yellow protein (PYP) is a novel type of photoreceptor containing a thiol ester-l...
Biological signal transduction starts with the activation of a receptor protein. Two central questio...
ABSTRACT: Biological signal transduction starts with the activation of a receptor protein. Two centr...
The ability to avoid blue-light radiation is crucial for bacteria to survive. In Halorhodospira halo...
ABSTRACT: Photoactive yellow protein (PYP) is a bacterial blue light sensor that induces Halorhodosp...
The recovery reaction of the signaling state of photoactive yellow protein includes the following: (...
AbstractAs a bacterial blue light sensor the photoactive yellow protein (PYP) undergoes conformation...
In this study we have investigated binding of the fluorescent hydrophobicity probe Nile Red to the p...
The bacterial photoreceptor protein photoactive yellow protein (PYP) covalently binds the chromophor...
The ultrafast excited-state dynamics underlying the receptor state photorecovery is resolved in the ...
ABSTRACT In this study we have investigated binding of the fluorescent hydrophobicity probe Nile Red...
The bacterial photoreceptor protein photoactive yellow protein (PYP) covalently binds the chromophor...
AbstractAs a bacterial blue light sensor the photoactive yellow protein (PYP) undergoes conformation...
AbstractVisualizing the three-dimensional structures of a protein during its biological activity is ...
Photoactive yellow protein (PYP) is a novel type of photoreceptor containing a thiol ester-linked p-...
AbstractPhotoactive yellow protein (PYP) is a novel type of photoreceptor containing a thiol ester-l...
Biological signal transduction starts with the activation of a receptor protein. Two central questio...
ABSTRACT: Biological signal transduction starts with the activation of a receptor protein. Two centr...
The ability to avoid blue-light radiation is crucial for bacteria to survive. In Halorhodospira halo...
ABSTRACT: Photoactive yellow protein (PYP) is a bacterial blue light sensor that induces Halorhodosp...
The recovery reaction of the signaling state of photoactive yellow protein includes the following: (...
AbstractAs a bacterial blue light sensor the photoactive yellow protein (PYP) undergoes conformation...
In this study we have investigated binding of the fluorescent hydrophobicity probe Nile Red to the p...
The bacterial photoreceptor protein photoactive yellow protein (PYP) covalently binds the chromophor...
The ultrafast excited-state dynamics underlying the receptor state photorecovery is resolved in the ...
ABSTRACT In this study we have investigated binding of the fluorescent hydrophobicity probe Nile Red...
The bacterial photoreceptor protein photoactive yellow protein (PYP) covalently binds the chromophor...
AbstractAs a bacterial blue light sensor the photoactive yellow protein (PYP) undergoes conformation...
AbstractVisualizing the three-dimensional structures of a protein during its biological activity is ...