High-pressure NMR study of the dissociation of Arc repressor. 1994

X Peng, and J Jonas, and J L Silva
School of Chemical Sciences, University of Illinois, Urbana 61801.

Different denatured states of Arc repressor were characterized by one-dimensional and two-dimensional NMR and by fluorescence spectroscopy. Increasing pressure promoted sequential changes in the structure of Arc repressor: from the native dimer through a predissociated state to a denatured molten globule monomer. A compact state (molten globule) of Arc repressor was obtained in the dissociation of Arc repressor by pressure whereas high temperature and urea induced dissociation and unfolding to less structured conformations. The NMR spectra of the monomer under pressure (up to 5.0 kbar) are typical of a molten globule, and they are considerably different from those of the native dimer and the thermally or chemically denatured monomer. The substantial line broadening and overlap of many resonances in the NMR spectra at high pressures indicate that there is interconversion between a number of different conformations of the molten globule at an intermediate exchange rate. The two-dimensional NOE spectra show that the pressure-denatured monomer retains substantial secondary structure. The presence of NOEs in the beta-sheet region in the dissociated state suggests that the intersubunit beta-sheet (residues 6-14) in the native-dimer is replaced by an intramonomer beta-sheet. Changes in 2D NMR spectra prior to dissociation indicate the existence of a predissociated state that may represent an intermediate in the folding and subunit association pathway of Arc repressor.

UI MeSH Term Description Entries
D009682 Magnetic Resonance Spectroscopy Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING). In Vivo NMR Spectroscopy,MR Spectroscopy,Magnetic Resonance,NMR Spectroscopy,NMR Spectroscopy, In Vivo,Nuclear Magnetic Resonance,Spectroscopy, Magnetic Resonance,Spectroscopy, NMR,Spectroscopy, Nuclear Magnetic Resonance,Magnetic Resonance Spectroscopies,Magnetic Resonance, Nuclear,NMR Spectroscopies,Resonance Spectroscopy, Magnetic,Resonance, Magnetic,Resonance, Nuclear Magnetic,Spectroscopies, NMR,Spectroscopy, MR
D011312 Pressure A type of stress exerted uniformly in all directions. Its measure is the force exerted per unit area. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed) Pressures
D011489 Protein Denaturation Disruption of the non-covalent bonds and/or disulfide bonds responsible for maintaining the three-dimensional shape and activity of the native protein. Denaturation, Protein,Denaturations, Protein,Protein Denaturations
D012097 Repressor Proteins Proteins which maintain the transcriptional quiescence of specific GENES or OPERONS. Classical repressor proteins are DNA-binding proteins that are normally bound to the OPERATOR REGION of an operon, or the ENHANCER SEQUENCES of a gene until a signal occurs that causes their release. Repressor Molecules,Transcriptional Silencing Factors,Proteins, Repressor,Silencing Factors, Transcriptional
D013050 Spectrometry, Fluorescence Measurement of the intensity and quality of fluorescence. Fluorescence Spectrophotometry,Fluorescence Spectroscopy,Spectrofluorometry,Fluorescence Spectrometry,Spectrophotometry, Fluorescence,Spectroscopy, Fluorescence
D013696 Temperature The property of objects that determines the direction of heat flow when they are placed in direct thermal contact. The temperature is the energy of microscopic motions (vibrational and translational) of the particles of atoms. Temperatures
D014508 Urea A compound formed in the liver from ammonia produced by the deamination of amino acids. It is the principal end product of protein catabolism and constitutes about one half of the total urinary solids. Basodexan,Carbamide,Carmol
D014764 Viral Proteins Proteins found in any species of virus. Gene Products, Viral,Viral Gene Products,Viral Gene Proteins,Viral Protein,Protein, Viral,Proteins, Viral
D015394 Molecular Structure The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds. Structure, Molecular,Molecular Structures,Structures, Molecular
D017433 Protein Structure, Secondary The level of protein structure in which regular hydrogen-bond interactions within contiguous stretches of polypeptide chain give rise to ALPHA-HELICES; BETA-STRANDS (which align to form BETA-SHEETS), or other types of coils. This is the first folding level of protein conformation. Secondary Protein Structure,Protein Structures, Secondary,Secondary Protein Structures,Structure, Secondary Protein,Structures, Secondary Protein

Related Publications

X Peng, and J Jonas, and J L Silva
September 1989, Biochemistry,
X Peng, and J Jonas, and J L Silva
December 1986, Biochemistry,
X Peng, and J Jonas, and J L Silva
October 2006, Proteins,
X Peng, and J Jonas, and J L Silva
September 1985, Journal of molecular biology,
X Peng, and J Jonas, and J L Silva
July 1994, Journal of molecular biology,
X Peng, and J Jonas, and J L Silva
June 2005, Journal of molecular biology,
X Peng, and J Jonas, and J L Silva
January 2015, Sub-cellular biochemistry,
X Peng, and J Jonas, and J L Silva
November 1998, Journal of biomolecular NMR,
Copied contents to your clipboard!