Browsing by Author "Dhingra, M M"
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Item Assignment of ribose carbon-13 resonances of puromycin and its analogs by 2D NMR: correlation between resonance position and electronegativity.(1986-08-01) Narula, S S; Dhingra, M MItem Comparative study of conformational behaviour of leucine and methionine enkephalinamides by 1H-nuclear magnetic resonance spectroscopy.(1988-03) Dhingra, M M; Saran, AnilThe conformational proclivity of leucine and methionine enkephalinamides in deuterated dimethyl sulphoxide has been investigated using proton magnetic resonance at 500 MHz. The resonances from the spin system of the various amino acid residues have been assigned from the 2-dimensional correlated spectroscopy spectra. The temperature variation of the amide proton shifts indicates that none of the amide proton is intramolecularly hydrogen-bonded or solvent-shielded. The analysis of vicinal coupling constants, 3JHN.C 2 H,along with temperature coefficients and the absence of characteristic nuclear Overhauser effect cross peaks between the NH protons reveal that there is no evidence of the chain folding in these molecules. However, the observation of nuclear Overhauser effect cross peaks between the NH and the CαH of the preceding residue indicates preference for extended backbone conformation with preferred side chain orientations particularly of Tyr and Phe in both [Leu5] - and [Met5]-enkephalinamides.Item Conformational preference of Leu side chain in melanostatin in DMSO.(1990-04-01) Sasidhar, Y U; Dhingra, M M; Saran, AThe solution conformation of melanostatin (Pro-Leu-Gly-NH2) in the neutral and protonated forms of DMSO has been monitored by one and two dimensional NMR techniques at 500 MHz. The temperature coefficients of the amide proton chemical shifts in conjunction with the observed NOESY spectra suggest that melanostatin in neutral form in DMSO adopts a backbone conformation such that leucine amide proton is buried by the proline ring and the side chain of leucine. Similar observation is made for protonated form of melanostatin in DMSO. The results of the present study are at variance with the earlier NMR studies which proposed a beta-turn structure for both the forms of melanostatin. There is, however, no evidence for the presence of beta-turn structure for both the forms of melanostatin in DMSO. In CDCl3 also Leu NH appears to be buried as evident from the solvent titration with DMSO and NOESY spectra.Item Conformational studies on adenosine and its analogs by proton magnetic resonance.(1985-02-01) Narula, S S; Dhingra, M MItem Determination of ionization sites and pK values in puromycin and puromycin aminonucleoside by 13C and 1H magnetic resonance.(1986-12-01) Narula, S S; Dhingra, M MItem Interaction of puromycin and puromycin aminonucleoside with poly (A)--a proton magnetic resonance investigation.(1986-12-01) Dhingra, M M; Narula, S SItem A new bioluminescent fungal system.(1983-03) Sabharwal, S C; Kathuria, S P; Dhingra, M MA new bioluminescent fungal system from a wood sample with a characteristic emission around 518 ± 1 nm is described. This study indicates that water is not only important for emission but has a function in the kinetics of the reaction.Item Solution conformation of a model hexapeptide containing RGD sequence.(1992-12-01) Dhingra, M MThe solution conformation of a model hexapeptide Asp-Arg-Gly-Asp-Ser-Gly (DRGDSG) containing the RGD sequence has been studied in DMSO-d6 as well as in aqueous solution (H2O:D2O/90:10%) by 1H NMR spectroscopy. The unambiguous identification of spin systems of various amino acid residues and sequence specific assignment of all proton resonances was achieved by a combination of two dimensional COSY and NOESY experiments. The temperature coefficient data of the amide proton chemical shifts in conjunction with the vicinal coupling constants, i.e. 3JNH-C alpha H, NOESY and ROESY results indicate that the peptide in both the solvents exists in a blend of conformers with beta-sheet like extended backbone structure and folded conformations. The folded conformers do not appear to be stabilised by intramolecular hydrogen bonding. Our results are consistent with the flexibility of RGD segment observed in the NMR studies on the protein echistatin containing the RGD motif (references 23-25).