Modifications of the Rate Matrix Required for the Quantitative Analysis of NOESY Spectra of Proteins
β Scribed by M.J. Dellwo; D.M. Schneider; A.J. Wand
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 886 KB
- Volume
- 103
- Category
- Article
- ISSN
- 1064-1866
No coin nor oath required. For personal study only.
β¦ Synopsis
The introduction of rate matrix analysis to protocols for the refinement of solution structures of biopolymers on the basis of NMR-derived structural constraints has greatly enhanced the self-consistency of the general approach. However, current implementations of this strategy appear not to consider several issues arising from various commonly employed experimental conditions and sample characteristics which can prevent the quantitative interpretation of NOESY spectra of proteins. Here, a number of these effects are considered, including the influence of nonequilibrium populations generated by over-pulsing and solvent presaturation, the presence of heteronuclei, and the equilibration of exchangeable sites with deuterium in solvent. The modifications of the rate matrix that are required to treat these effects are summarized and simulations presented to illustrate the relative importance of each. The computational effort required to rigorously accommodate each effect is described along with several simple experimental modifications that reduce the computational burden.
π SIMILAR VOLUMES
RELAX is a flexible program for the quantitative analysis of NOESY spectra. It allows the simultaneous application of different models describing the internal and overall motion of the molecule under investigation for individual spin pairs or groups of spins. A correction for anisotropy effects due
This paper uses a modification of the continuous time asset pricing model of Cox, Ingersoll, and Ross to analyze the effect of regulatory risk on the cost of capital. Analysis shows that random errors in setting the allowed rate of return can either increase or decrease the cost of capital depending
Conditions are described by which cells and fresh frozen tissues, following fixation with ethanol-ether, and after staining with the amidoblack (AB)-TCA-staining method, show a modified dye/protein ratio of 0.9 moles AB/10(5) g protein compared to 8.5 moles AB/10(5) g protein ( Schauenstein et al. 1