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tracer

The Columbia Encyclopedia, Sixth Edition | Date: 2008

tracer an identifiable substance used to follow the course of a physical, chemical, or biological process. In chemistry the ideal tracer has the same chemical properties as the molecule it replaces and undergoes the same reactions but can at all times be detectible and quantitatively assessed. In biochemistry tracers have been in use since the beginning of the 20th cent. Using synthetic methods, Franz Knoop in 1904 made various derivatives of fatty acids, the degradation of which he studied by feeding the derivatives to dogs and by monitoring the appearance of unusual products in the dogs' urine. From these studies were obtained the first descriptions of the metabolic pathway for fatty acid catabolism. About these sorts of experiments, however, the argument could always be made that the derivatives were "unphysiological," that is, did not occur naturally and might be handled by the enzymes of the body differently than "physiological" compounds. This difficulty was overcome in 1935 when Rudolf Schoenheimer and David Rittenberg described the use of the isotope deuterium (identical to the hydrogen atom except that it contains an extra neutron) in following biochemical reactions. They argued persuasively that deuterium-labeled compounds (those having a deuterium atom substituted for a hydrogen) were essentially indistinguishable from nonlabeled compounds as far as metabolic processes were concerned but that the amount of deuterium in any given sample could be quantitatively determined by the properties of the water produced upon combustion of the sample. Although this was the first declaration of the general usefulness of the approach, George Hevesy in 1923 was the first investigator to use an isotope in metabolic studies; he explored lead transport in the bean plant using radioactive thorium. Radioactive isotopes are more easily detected than nonradioactive ones, such as deuterium; therefore, when the radioactive isotopes of various atoms commonly occurring in organic molecules became widely available after World War II, metabolic studies proliferated. Isotopes in common use today include carbon-14, iodine-131, nitrogen-15, oxygen-17, phosphorus-32, sulfur-35, tritium (hydrogen-3), iron-59, and sodium-24.

Author not available, TRACER., The Columbia Encyclopedia, Sixth Edition 2008

The Columbia Encyclopedia, Sixth Edition. Copyright 2008 Columbia University Press