ABSTRACT
The ion association complex formed with the cadmium chelate of the dimethyl ester of meso-2,3-dimercaptosuccinic acid and the tetramethylammonium cation, [(Me)4N]2[Cd(Di-MeDMSA)2], has been synthesized. The structures of the ion association complex and of the ligand (meso-DiMeDMSA) were determined by single-crystal X-ray diffraction. The two methyl ester groups and the two sulfhydryl groups in meso-DiMeDMSA were in a staggered conformation. The anion [Cd(DiMeDMSA)2]2- is essentially a distorted tetrahedron, with a mononuclear CdS4 kernel. The structure of the [Cd(DiMeDMSA)2]2- anion in solution was found to be similar to its structure in the solid state by multinuclear (1H, 13C, 113Cd) magnetic resonance spectroscopy. In the presence of rabbit liver metallothionein I (MT), meso-DiMeDMSA was found to coordinate Zn2+ and Cd2+ ions. 1H NMR spectroscopy proved to be an effective analytical technique for monitoring the competition between meso-DiMeDMSA and the protein for these metal ions. This was accomplished by probing the tertiary structure of MT with 1H NMR spectroscopy after incubation with meso-DiMeDMSA. In addition, the 1H NMR spectra of rabbit liver metallothionein I demonstrated that MT is more susceptible to oxidation at physiological pH after the metal ions have been removed. It appears that intra- as well as intermolecular disulfide cross-linkages are formed upon oxidation. When rabbit liver metallothionein I was incubated with meso-DiMeDMSA in a 20:1 (meso-DiMeDMSA:MT) mole ratio, 32% of the cadmium and 87% of the zinc bound to MT were removed.
Subject(s)
Cadmium/chemistry , Chelating Agents/chemistry , Liver/chemistry , Metallothionein/chemistry , Succimer/analogs & derivatives , Succimer/chemistry , Animals , Binding, Competitive/drug effects , Cadmium Radioisotopes , Chelating Agents/pharmacology , Magnetic Resonance Spectroscopy , Protein Binding , Rabbits , Solutions , Spectrophotometry, Atomic , Succimer/pharmacology , Temperature , Ultrafiltration , X-Ray Diffraction , Zinc/metabolismABSTRACT
C14H16N2, Mr = 212.3, orthorhombic, Pca2(1), a = 19.424 (3), b = 6.770 (1), c = 8.899 (1) A, V = 1170.2 (3) A3, Z = 4, Dx = 1.20 g cm-3, Mo K alpha, lambda = 0.71073 A, mu = 0.7 cm-1, F(000) = 456, T = 296 K, final R = 0.043 for 1162 observed reflections. The pi systems in the title compound (1), a serotonin mimic, are in a 'near-planar' conformation (actually twisted 21 degrees from the transoid conformation) as has been postulated to be essential for activity. Molecular-mechanics calculations indicate that the inactive 2-methyl derivative of (1) has near-planar forms of much higher energy in accordance with expectation.
Subject(s)
Carbolines , Chemical Phenomena , Chemistry, Physical , Crystallization , Crystallography , Molecular Conformation , Molecular StructureABSTRACT
The pH-dependent structure of calf thymus DNA is analyzed using Raman spectroscopy. The Raman spectra in the acidic region demonstrate that denaturation occurs in several steps. The binding of H+ to adenine and cytosine residues is accompanied by a decrease in the percentage of DNA in the B-conformation and a concurrent increase in a conformation most probably related to the C-form. The denaturation of DNA is observed at pH 3.3 and parallels the protonation of guanine bases. The Raman spectra of calf thymus DNA in the basic region (above pH 10) show that guanine residues are deprotonated at lower pH value than are thymine residues. In addition, Raman spectra in the basic region detect conformational changes of the phosphate backbone different from those found in the acidic region.
