Time-resolved CIDNP study of protein-related molecules

نویسندگان

  • Olga Morozova
  • Alexandra Yurkovskaya
  • Yuri Tsentalovich
  • Renad Sagdeev
چکیده

Time-resolved CIDNP and Laser Flash Photolysis have been applied to the investigation of the kinetics and mechanism of CIDNP formation in the reactions of aza-aromatic dye 2,2′-dipyridyl and protein-related molecules, including N-acetyl derivatives of three amino acids (tryptophan, tyrosine, histidine) the dipeptide tryptophan-tyrosine, and hen egg-white lysozyme in native and denatured states. CIDNP kinetics for the dipeptide is affected by intramolecular electron transfer from tyrosine residue to the oxidized tryptophan residue. The peculiarities of CIDNP kinetic behavior in the presence of IET are studied for the denatured state of lysozyme. In the native state, IET was found to be ineffective.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

19F NMR studies of the native and denatured states of green fluorescent protein.

Biosynthetic preparation and (19)F NMR experiments on uniformly 3-fluorotyrosine-labeled green fluorescent protein (GFP) are described. The (19)F NMR signals of all 10 fluorotyrosines are resolved in the protein spectrum with signals spread over 10 ppm. Each tyrosine in GFP was mutated in turn to phenylalanine. The spectra of the Tyr --> Phe mutants, in conjunction with relaxation data and resu...

متن کامل

Rapid formation of non-native contacts during the folding of HPr revealed by real-time photo-CIDNP NMR and stopped-flow fluorescence experiments.

We report the combined use of real-time photo-CIDNP NMR and stopped-flow fluorescence techniques to study the kinetic refolding of a set of mutants of a small globular protein, HPr, in which each of the four phenylalanine residues has in turn been replaced by a tryptophan residue. The results indicate that after refolding is initiated, the protein collapses around at least three, and possibly a...

متن کامل

Electron and hydrogen self-exchange of free radicals of sterically hindered tertiary aliphatic amines investigated by photo-CIDNP

The photoreactions of diazabicyclo[2,2,2]octane (DABCO) and triisopropylamine (TIPA) with the sensitizers anthraquinone (AQ) and xanthone (XA) or benzophenone (BP) were investigated by time-resolved photo-CIDNP (photochemically induced dynamic nuclear polarization) experiments. By varying the radical-pair concentration, it was ensured that these measurements respond only to self-exchange reacti...

متن کامل

CIDNP Effects of Sensitized Photochemical Dediazoniation of Arene Diazonium Salts Manipulating CIDNP Intensities by the Experimental Conditions

13C and 15N photo-CIDNP effects were determined for the reversible electron transfer from pyrene to arene diazonium salts on excitation of the charge transfer band at 360 nm. The diazonium salts being the products of back electron transfer ("cage products") show enhanced absorption for 13C(1) and the 15N-enriched diazonium group, whereas the escape products, ArH or löN2, respectively, yield emi...

متن کامل

Level crossing analysis of chemically induced dynamic nuclear polarization: Towards a common description of liquid-state and solid-state cases.

Chemically Induced Dynamic Nuclear Polarization (CIDNP) is an efficient method of creating non-equilibrium polarization of nuclear spins by using chemical reactions, which have radical pairs as intermediates. The CIDNP effect originates from (i) electron spin-selective recombination of radical pairs and (ii) the dependence of the inter-system crossing rate in radical pairs on the state of magne...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2002