Literature DB >> 6378910

Structure-function relationship in Escherichia coli translational initiation factors. Characterization of IF-3 by high resolution 1H NMR spectroscopy.

M Paci, C Pon, M Lammi, C Gualerzi.   

Abstract

Translational initiation factor-3 (IF-3) was characterized by 1H NMR spectroscopy as a function of pH and temperature and following chemical modifications. Spin-lattice relaxation times for individual resonances and bands were also measured. Several resonances were assigned to different amino acid residues by different criteria. Among these are the CH3-N of the N-terminal methionine which appears free, mobile, and very sensitive to the modification of several physicochemical parameters as well as the 3,5 and 2,6 protons of the three tyrosines (two of which play a role in the function of IF-3) which were found to be located in different magnetic environments. Two of these residues appear to be close to each other and in the vicinity of a slow reacting arginine within the tertiary structure of the factor. The properties and the titration behavior of the imidazole proton resonances suggest that the single His residue is partially buried in the protein structure. Characteristic of the IF-3 spectrum also is the presence of an abundant subset of Arg delta-CH2, Lys epsilon-CH2, and CH3 protons displaying clear cut upfield perturbations. These are probably due to the coming together of two or more apolar "fronts" which possibly arise from distant parts of the molecule and result in the close proximity between aromatic rings and aliphatic side chains. The IF-3 spectrum also includes several distinct methyl resonances significantly shifted upfield by aromatic ring currents. Overall, the characteristics of the spectrum, its relative insensitivity to temperature and ionic strength, and the existence of extensive cross-relaxation phenomena indicate that IF-3 has a highly folded tertiary structure with abundant hydrophobic regions. In spite of some heterogeneity in the distribution of the side chain environments, no indication was found for the existence of distinct domains or, at least, of extensive regions with higher mobility.

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Year:  1984        PMID: 6378910

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  3 in total

1.  Evidence for an active role of IF3mt in the initiation of translation in mammalian mitochondria.

Authors:  Brooke E Christian; Linda L Spremulli
Journal:  Biochemistry       Date:  2009-04-21       Impact factor: 3.162

2.  Structural and Functional Elucidation of IF-3 Protein of Chloroflexus aurantiacus Involved in Protein Biosynthesis: An In Silico Approach.

Authors:  Abu Saim Mohammad Saikat; Md Ekhlas Uddin; Tasnim Ahmad; Shahriar Mahmud; Md Abu Sayeed Imran; Sohel Ahmed; Salem A Alyami; Mohammad Ali Moni
Journal:  Biomed Res Int       Date:  2021-07-01       Impact factor: 3.411

3.  The interaction of mammalian mitochondrial translational initiation factor 3 with ribosomes: evolution of terminal extensions in IF3mt.

Authors:  Md Emdadul Haque; Domenick Grasso; Linda L Spremulli
Journal:  Nucleic Acids Res       Date:  2007-12-01       Impact factor: 16.971

  3 in total

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