Abstract
A new caged proton, 1-(2-nitrophenyl)ethyl sulfate (caged sulfate), is characterized by infrared spectroscopy and compared with a known caged, proton 2-hydroxyphenyl 1-(2-nitrophenyl)ethyl phosphate (caged HPP). In contrast to caged HPP, caged sulfate can induce large pH jumps and protonate groups that have pK values as low as 2.2. The photolysis mechanism of caged sulfate is analogous to that of P(3)-[1-(2-nitrophenyl)ethyl] ATP (caged ATP), and the photolysis efficiency is similar. The utility of this new caged compound for biological studies was demonstrated by its ability to drive the acid-induced conformational change of metmyoglobin. This transition from the native conformation to a partially unfolded form takes place near pH 4 and was monitored by near-UV absorption spectroscopy.
MeSH Terms
Biophysical Phenomena
Biophysics
Carboxylic Acids/chemistry
Hydrogen/chemistry
Hydrogen-Ion Concentration
Light
Metmyoglobin/chemistry
Models, Chemical
Nitrobenzenes/chemistry,pharmacology
Organophosphates/chemistry
Protein Conformation
Protons
Spectrophotometry
Spectroscopy, Fourier Transform Infrared/methods
Sulfates/chemistry
Ultraviolet Rays
Chemicals
1-(2-nitrophenyl)ethyl sulfate
Carboxylic Acids
Nitrobenzenes
Organophosphates
Protons
Sulfates
Metmyoglobin
2-hydroxyphenyl 1-(2-nitrophenyl)ethyl phosphate
Hydrogen
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Barth Andreas
Institut für Biophysik, Johann Wolfgang Goethe-Universität, D-60590 Frankfurt am Main, Germany.
Corrie John E T
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