Abstract
Although remarkable progress has been achieved in the past decades towards an understanding of the structure and function of the ribosome, the interactions of nucleic acids and proteins involved in protein biosynthesis remain largely unresolved. It has convincingly been demonstrated that ribosomal RNA is essential for ribosomal function (e.g. Schulze and Nierhaus, 1982; Dahlberg, 1989; Noller et al., 1992), yet there can be no doubt that in contemporary ribosomes complexes of RNA and proteins constitute the functional units.Models of the tertiary structure of the 16S RNA have been derived from footprinting and crosslinking experiments (Stern et al., 1988; Brimacombe et al., 1988; Nagano et al., 1988). In addition, functionally important domains and even nucleotides were identified by affinity labelling and site-directed mutagenesis.
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Kruft, V., Bischof, O., Bergmann, U., Herfurth, E., Wittmann-Liebold, B. (1993). Towards Ribosomal Structure at Peptide Level: Use of Crosslinking, Antipeptide Antibodies and Limited Proteolysis. In: Nierhaus, K.H., Franceschi, F., Subramanian, A.R., Erdmann, V.A., Wittmann-Liebold, B. (eds) The Translational Apparatus. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-2407-6_48
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