“…The available data sets include determinations of the spatial distribution of the ribosomal proteins by neutron scattering or immuno-electron microscopy (IEM), analyses of contacts or neighbourhoods between ribosomal proteins and rRNA by cross-linking and foot-printing techniques, analyses of neighbourhoods within or between the rRNA molecules by intra or interrRNA cross-linking, and studies on the location of the rRNA relative to functional ligands such as mRNA and tRNA, again with the help of crosslinking and foot-printing methods (for reviews, see Brimacombe, 1995;Noller et al, 1995). A number of research groups (Expert-Bezanc Ëon & Wollenzien, 1985;Brimacombe et al, 1988;Nagano et al, 1988;Stern et al, 1988;Mitchell et al, 1990;Hubbard & Hearst, 1991;Malhotra & Harvey, 1994;Fink et al, 1996) have made use of these types of data to fold the well-established secondary structures of the 16 S and 23 S rRNA molecules into three dimensions. The resulting 3D models are essentially``cartoon'' structures of the ribosomal subunits, in which the various helical elements of the rRNA have been manoeuvred relative to the ribosomal proteins so as to satisfy as many of the topographical constraints as possible.…”