ArticleMethods (San Diego, Calif.)2011
The boundary structure in the analysis of reversibly interacting systems by sedimentation velocity.
Article in Methods (San Diego, Calif.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
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Who cites it
23 citing papers in PubMed.
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- KRAS Prenylation Is Required for Bivalent Binding with Calmodulin in a Nucleotide-Independent Manner.Biophysical journal · 2019Article
- Article
- Hysteresis and Allostery in Human UDP-Glucose Dehydrogenase Require a Flexible Protein Core.Biochemistry · 2018Article
- Use of fluorescence-detected sedimentation velocity to study high-affinity protein interactions.Nature protocols · 2017Article
- Sedimentation of Reversibly Interacting Macromolecules with Changes in Fluorescence Quantum Yield.Biophysical journal · 2017Article
- Allostery and Hysteresis Are Coupled in Human UDP-Glucose Dehydrogenase.Biochemistry · 2017Article
- Effect of arginine on oligomerization and stability of N-acetylglutamate synthase.Scientific reports · 2016Article
- 3D-Printing for Analytical Ultracentrifugation.PloS one · 2016Article
- Unique Role of the WD-40 Repeat Protein 5 (WDR5) Subunit within the Mixed Lineage Leukemia 3 (MLL3) Histone Methyltransferase Complex.The Journal of biological chemistry · 2015Article
- A histogram approach to the quality of fit in sedimentation velocity analyses.Analytical biochemistry · 2015Article
- Combining biophysical methods for the analysis of protein complex stoichiometry and affinity in SEDPHAT.Acta crystallographica. Section D, Biological crystallography · 2015Article
- Recorded scan times can limit the accuracy of sedimentation coefficients in analytical ultracentrifugation.Analytical biochemistry · 2013Article
- Analytical Ultracentrifugation as a Tool for Studying Protein Interactions.Biophysical reviews · 2013Article
- Analytical ultracentrifugation studies of oligomerization and DNA-binding of TtCarH, a Thermus thermophilus coenzyme B12-based photosensory regulator.European biophysics journal : EBJ · 2013Article
- Molecular model of a soluble guanylyl cyclase fragment determined by small-angle X-ray scattering and chemical cross-linking.Biochemistry · 2013Article
- Overview of current methods in sedimentation velocity and sedimentation equilibrium analytical ultracentrifugation.Current protocols in protein science · 2013Article
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4 authors.
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Abstract
Sedimentation velocity (SV) experiments of heterogeneous interacting systems exhibit characteristic boundary structures that can usually be very easily recognized and quantified. For slowly interacting systems, the boundaries represent concentrations of macromolecular species sedimenting at different rates, and they can be interpreted directly with population models based solely on the mass action law. For fast reactions, migration and chemical reactions are coupled, and different, but equally easily discernable boundary structures appear. However, these features have not been commonly utilized for data analysis, for the lack of an intuitive and computationally simple model. The recently introduced effective particle theory (EPT) provides a suitable framework. Here, we review the motivation and theoretical basis of EPT, and explore practical aspects for its application. We introduce an EPT-based design tool for SV experiments of heterogeneous interactions in the software SEDPHAT. As a practical tool for the first step of data analysis, we describe how the boundary resolution of the sedimentation coefficient distribution c(s) can be further improved with a Bayesian adjustment of maximum entropy regularization to the case of heterogeneous interactions between molecules that have been previously studied separately. This can facilitate extracting the characteristic boundary features by integration of c(s). In a second step, these are assembled into isotherms as a function of total loading concentrations and fitted with EPT. Methods for addressing concentration errors in isotherms are discussed. Finally, in an experimental model system of alpha-chymotrypsin interacting with soybean trypsin inhibitor, we show that EPT provides an excellent description of the experimental sedimentation boundary structure of fast interacting systems.
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