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Nucleotide sequence of nuclear 5.7S RNA of mouse cells
Authors:N Kato  F Harada
Institution:1. I.N.S.E.R.M. - Unité 95, Plateau de Brabois, 54500 Vandoeuvre, France.;2. Laboratoire de Chimie Physique Organique, Faculté des Sciences, C.O. 140, 54037 Nancy Cedex, France.;3. Service de Chimie Physique, UER Chimie, Faculté des Sciences, 44000 Nantes, France.;4. Department of Medicine, University of Cambridge, Addenbrooke''s Hospital, Level 5, Hills Road, Cambridge CB2 2QQ, England.
Abstract:Viable tumor cells were examined by 19F-NMR spectroscopy after treatment with 4-trifluoromethyl 2,6-dinitrophenyl sulphonate (CF3-DNBS), which is an analog of 2,4,6-trinitrophenyl sulphonate (TNBS). The presence of a strong 19F-NMR signal from treated cells suggested the binding of the “probe”. Treatment of labelled cells with proteolytic enzymes significantly decreased the signals, suggesting that the label was essentially bound to the cell surface macromolecules. A proportion of the material bound to the cell was removable by dialysis of cell extracts against a structural analog, suggesting that some CF3-DNBS-cell membrane bonds were not covalent. The existence of such non-covalent bonds has also been confirmed with soluble proteins. By the same approach, it was also found that 14C-TNBS formed covalent and non-covalent bonds with tumor cells.
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