Overview of current methods in sedimentation velocity and sedimentation equilibrium analytical ultracentrifugation.
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Complexes of neutralizing and non-neutralizing affinity matured Fabs with a mimetic of the internal trimeric coiled-coil of HIV-1 gp41MCM ring hexamerization is a prerequisite for DNA-binding.On the acquisition and analysis of microscale thermophoresis data.The DnaK Chaperone Uses Different Mechanisms To Promote and Inhibit Replication of Vibrio cholerae Chromosome 2.Analytical ultracentrifugation with fluorescence detection system reveals differences in complex formation between recombinant human TNF and different biological TNF antagonists in various environments.Sirt1 carboxyl-domain is an ATP-repressible domain that is transferrable to other proteins.An allosteric site in the T-cell receptor Cβ domain plays a critical signalling role.Improved measurement of the rotor temperature in analytical ultracentrifugation.SEDFIT-MSTAR: molecular weight and molecular weight distribution analysis of polymers by sedimentation equilibrium in the ultracentrifuge.Initiator protein dimerization plays a key role in replication control of Vibrio cholerae chromosome 2Multi-signal sedimentation velocity analysis with mass conservation for determining the stoichiometry of protein complexes.Analysis of high affinity self-association by fluorescence optical sedimentation velocity analytical ultracentrifugation of labeled proteins: opportunities and limitations.Nuclear Magnetic Resonance Structural Mapping Reveals Promiscuous Interactions between Clathrin-Box Motif Sequences and the N-Terminal Domain of the Clathrin Heavy Chain.A histogram approach to the quality of fit in sedimentation velocity analyses.Elucidating Complicated Assembling Systems in Biology Using Size-and-Shape Analysis of Sedimentation Velocity Data.Variable-Field Analytical Ultracentrifugation: I. Time-Optimized Sedimentation Equilibrium.3D-Printing for Analytical UltracentrifugationHfqs in Bacillus anthracis: Role of protein sequence variation in the structure and function of proteins in the Hfq familyFarnesylated and methylated KRAS4b: high yield production of protein suitable for biophysical studies of prenylated protein-lipid interactions.Sequential Engagement of Distinct MLKL Phosphatidylinositol-Binding Sites Executes Necroptosis.Interaction of TAPBPR, a tapasin homolog, with MHC-I molecules promotes peptide editing.Nucleophosmin integrates within the nucleolus via multi-modal interactions with proteins displaying R-rich linear motifs and rRNA.Variable Field Analytical Ultracentrifugation: II. Gravitational Sweep Sedimentation Velocity.Biochemical Roles for Conserved Residues in the Bacterial Fatty Acid-binding Protein Family.Multiple Weak Linear Motifs Enhance Recruitment and Processivity in SPOP-Mediated Substrate Ubiquitination.Analytical Ultracentrifugation as a Tool for Studying Protein Interactions.Recorded scan times can limit the accuracy of sedimentation coefficients in analytical ultracentrifugation.Higher-order oligomerization promotes localization of SPOP to liquid nuclear speckles.Monochromatic multicomponent fluorescence sedimentation velocity for the study of high-affinity protein interactions.'AND' logic gates at work: Crystal structure of Rad53 bound to Dbf4 and Cdc7.Improving the thermal, radial, and temporal accuracy of the analytical ultracentrifuge through external referencesTransient HIV-1 Gag-protease interactions revealed by paramagnetic NMR suggest origins of compensatory drug resistance mutations.Structural basis of recognition of farnesylated and methylated KRAS4b by PDEδ.Solution properties of γ-crystallins: hydration of fish and mammal γ-crystallins.The cytoplasmic domain of the T-cell receptor zeta subunit does not form disordered dimers.Human herpesvirus 7 U21 tetramerizes to associate with class I major histocompatibility complex molecules.Analysis of protein interactions with picomolar binding affinity by fluorescence-detected sedimentation velocity.Sedimentation of Reversibly Interacting Macromolecules with Changes in Fluorescence Quantum Yield.Biophysical and Structural Characterization of the Centriolar Protein Cep104 Interaction NetworkEvidence that avian reovirus σNS is an RNA chaperone: implications for genome segment assortment.
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P2860
Overview of current methods in sedimentation velocity and sedimentation equilibrium analytical ultracentrifugation.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Overview of current methods in ...... nalytical ultracentrifugation.
@en
type
label
Overview of current methods in ...... nalytical ultracentrifugation.
@en
prefLabel
Overview of current methods in ...... nalytical ultracentrifugation.
@en
P2860
P1476
Overview of current methods in ...... analytical ultracentrifugation
@en
P2093
Huaying Zhao
Rodolfo Ghirlando
P2860
P304
P356
10.1002/0471140864.PS2012S71
P478
Chapter 20
P577
2013-02-01T00:00:00Z