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• W1605681804 abstract "A new labelling technique in vivo has been introduced which allows the tritiation of cell components with high specific activity during growth in rich medium. By this technique the pool size of each protein can be measured directly in the supernatant from centrifugation at 150000 × g. A measurable pool was found for the proteins S1, S2, S6, S10, L1, L4, L7, L8/9, L10, L12, L21, and L25. Experiments on migration of ribosomal proteins from the supernatant to ribosomes (i.e. association) and vice versa (dissociation) demonstrate a remarkable constancy in the composition of the ribosome. There is no significant difference between ribosomes engaged or not engaged in poly-(Phe) synthesis." @default.
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• W1605681804 date "1975-09-01" @default.
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• W1605681804 title "Pools of Ribosomal Proteins in Escherichia coli. Studies on the Exchange of Proteins between Pools and Ribosomes" @default.
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• W1605681804 doi "https://doi.org/10.1111/j.1432-1033.1975.tb02275.x" @default.
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