Interaction of 16S rRNA With Protein S4 - a first step to visualization of the assembly of the Escherichia Coli 30S Ribosomal Subunit by Stem
Understanding the mechanism of ribosome assembly and involvement in protein synthesis can be greatly facilitated by elucidation of its three-dimensional structure. The conformation, topography, and Interactions of ribosomal constituent proteins and RNAs can be directly studied by dedicated high resolution scanning transmission electron microscopy (STEM). The high (80%) efficiency in collection of scattered electrons in the dark-field mode makes 1t possible to visualize freezedried unstained specimens at low radiation dose (le/Å2); this minimizes many artifacts inherent in conventional transmission electron microscopy (staining, air-dry1ng, and radiation damage). In addition, the linear proportionality of the large-angle elastically scattered electrons to specimen mass thickness can be used for quantitative determination of molecular weight, mass distribution, and calculation of the apparent radius of gyration (RG), a parameter closely related to the threedimensional structure of the macromolecule.