Proton fourier transform NMR studies of insulin: coordination of calcium to the Glu(B13) site drives hexamer assembly and induces a conformation change

Biochemistry ◽  
1988 ◽  
Vol 27 (9) ◽  
pp. 3387-3397 ◽  
Author(s):  
Richard Palmieri ◽  
Robert W. K. Lee ◽  
Michael F. Dunn
1978 ◽  
Vol 150 (2) ◽  
pp. 171-177 ◽  
Author(s):  
Terence N. Mitchell ◽  
Heinrich C. Marsmann

2014 ◽  
Vol 67 (7) ◽  
pp. 1021 ◽  
Author(s):  
Sonya K. Adas ◽  
Jesus A. Ocana ◽  
Scott D. Bunge

The addition of either lithium dimethylamide or lithium diethylamide to a tetrahydrofuran (THF) solution of 1,3-dicyclohexylcarbodiimide yielded THF adducts of lithium 2,2-dimethyl-1,3-dicyclohexylguandidinate (1) and lithium 2,2-diethyl-1,3-dicyclohexylguandidinate (2), respectively. One equivalent of either 1 or 2 was subsequently reacted with one equivalent of Group 11 halide (CuCl, AgBr, and AuCl) to generate oligonuclear complexes with the general formula {M[CyNC(NR2)NCy]}n where M, R, and n are respectively Cu, CH3, 2 (3); Cu, CH2CH3, 2 (4); Ag, CH3, 3 (5); Ag, CH2CH3, 3 (6); Au, CH3, 2 (7); and Au, CH2CH3, 2 (8). Compounds 1–8 were characterized by single-crystal X-ray diffraction. The bulk powders for all complexes were found to be in agreement with the crystal structures based on elemental analyses, Fourier transform infrared spectroscopy, and 1H, 13C, and 7Li NMR studies. The unique structural aspects of this family of Group 11 complexes are highlighted.


FEBS Letters ◽  
1984 ◽  
Vol 169 (1) ◽  
pp. 107-111 ◽  
Author(s):  
F.J.M. van de Ven ◽  
S.H. de Bruin ◽  
C.W. Hilbers

1984 ◽  
Vol 15 (40) ◽  
Author(s):  
M. POPE ◽  
P. MASCAGNI ◽  
W. A. GIBBONS ◽  
L. M. CIUFFETTI ◽  
H. W. KNOCHE

1992 ◽  
Vol 25 (2) ◽  
pp. 165-170 ◽  
Author(s):  
A. Veijanen ◽  
E. Kolehmainen ◽  
R. Kauppinen ◽  
M. Lahtiperä ◽  
J. Paasivirta

Off-flavour compounds produced by algae in freshwater ecosystems were studied for their structure using integrated sensory and spectroscopic methods: mass spectrometry (MS), nuclear magnetic resonance (NMR) and Fourier transform infrared (FTIR). Both solvent extraction and thermal desorption were used to isolate and to introduce the compounds into gas chromatography/mass spectrometry (GC/MS) and gas chromatography/Fourier transform infrared (GC/FTIR) systems. Ten ng of a terpenoid compound gave a readable IR spectrum. For 1H NMR studies the compounds were collected directly into NMR solvent by preparative gas chromatography. About 5 µg of a monoterpenoid compound was needed for a reliable 1H NMR spectrum. The mass spectral data indicated that the series of odorous substances detected by GC were terpenoid hydrocarbons and a later eluting series of compounds were sesquiterpene alcohols. In addition, one compound with an intense off-odour (aromatic, nitrogen containing compound) and some tainting carboxylic acids (derived from a starch factory) were detected.


Sign in / Sign up

Export Citation Format

Share Document