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Intrinsic structural differences between ‘tight couples’ and Kaltschmidt–Wittmann ribosomes evidenced by dielectric spectroscopy and scanning microcalorimetry
Author(s) -
Bonincontro A,
Nierhaus K.H,
Onori G,
Risuleo G
Publication year - 2001
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(00)02415-7
Subject(s) - isothermal microcalorimetry , ribosome , differential scanning calorimetry , relaxation (psychology) , dielectric , 30s , spectroscopy , analytical chemistry (journal) , phase (matter) , crystallography , solvent , chemistry , materials science , chromatography , biology , rna , biochemistry , thermodynamics , organic chemistry , physics , optoelectronics , quantum mechanics , neuroscience , enthalpy , gene
Measurements of dielectric spectroscopy (DS) and microcalorimetry (differential scanning calorimetry (DSC)) of Escherichia coli 70S, 50S and 30S were performed on particles prepared according either to the ‘classical’ twice NH 4 Cl‐washed ribosomes, also known as loose couples (LC), or to the ‘tight couples’ preparative protocol (TC). Results show that 70S particles prepared according to the two different protocols exhibit different structural properties. Two subsequent relaxation processes occur in both samples as measured by DS. However, in LC ribosomes the first one is shifted towards a lower frequency with a higher dielectric increment. This is suggestive of a more extensive exposure of RNA to the solvent and of an overall more relaxed structure. The smaller LC subunit exhibits only one relaxation while the TC 30S shows two dielectric dispersions as well as 70S. No substantial differences were evidenced in either 50S species. Two typical melting peaks were observed by DSC both in LC and TC 70S as well as in 50S. Thermograms obtained from the TC 30S show a single well structured peak while LC particles produce a large unstructured curve. On the basis of these results we conclude that TC 70S particles are more compact than LC ribosomes and that in the former ones the rRNA is less exposed to the solvent phase. Furthermore 30S particles obtained from TC show a more stable structure with respect to LC 30S. We conclude that the 30S subunit gives a major contribution to the compact character of the whole TC 70S. These differences might be related to the intrinsic and well documented functional difference between the two ribosome species.