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1  to bind Fg when they were destabilized by a chaotrope.
2  in vivo as compared with amyloids formed in chaotropes.
3 arent weakening of the hydrophobic effect by chaotropes.
4 mental changes such as low concentrations of chaotropes.
5 LC, gel electrophoresis, and dissociation by chaotropes.
6 eractions driven either by the presence of a chaotrope (a nonspecific trigger for aggregation) or by
7 that kosmotropes reduce evaporation, whereas chaotropes accelerate the evaporation process, following
8 1, and SOSIP.664 trimers) to explore how the chaotrope acts.
9 are compatible with solubility agents (e.g., chaotropes and detergents) known to improve enzymatic di
10 high thermostability, resist denaturation by chaotropes and organic solvents, and have applicability
11   Protein conformational stabilities against chaotropes and temperature were measured.
12                       This study developed a chaotrope- and label-free biolayer interferometry (BLI)
13 , I(foot)) prespike events are observed when chaotropes are counterions in the stimulation solution,
14 toward the surface normal in the presence of chaotropes at the air/water interface.
15 sion of kosmotropes from (or accumulation of chaotropes at) the surface, the kinetics proved to be mo
16                          Previously reported chaotrope-based avidity assays that rely on artificial d
17 osmotropic anions "make" water structure and chaotropes "break" it being countered by recent studies
18                     Arginine is a well-known chaotrope but increases surface tension of water.
19 me of the fusion pore are longer, suggesting chaotropes can extend the duration of exocytosis compare
20 cts of a range of temperature, pressure, and chaotrope concentrations were tested and led to optimal
21  elongation, whereas poorly hydrated anions (chaotropes) delay nucleation and mildly affect the elong
22                                              Chaotrope denaturation of TTR exhibits unusual behavior
23                                              Chaotrope-denatured amylin and amylin processing interme
24 asurements of the SCN(-) ion, a prototypical chaotrope, determined a free energy of adsorption within
25  (SPE) processes, a silica solid phase using chaotrope-driven binding and an ion exchange phase using
26 ls expressing CB(1) and CB(2) receptors were chaotrope extracted to denature endogenous GTP-binding p
27 developed an in situ reconstitution assay in chaotrope-extracted membranes from mouse fibroblasts exp
28              This rapid, easy to operate and chaotrope-free BLI assay is suitable for clinical use an
29 chaotropic from kosmotropic substances (i.e. chaotropes &gt;/= +4; kosmotropes </= -4 kJ kg(-1) mol(-1)
30 oxide dismutase (SOD1) dimers induced by the chaotrope guanidine hydrochloride (GdnHCl) or the reduct
31        Structural stability studies with the chaotrope guanidinium chloride revealed that there is mo
32 BioI secondary and tertiary structure by the chaotrope guanidinium chloride.
33 the precipitation of proteins, while others (chaotropes) increase their solubility.
34 ons the net effect of the linear, presumably chaotrope-induced deceleration and the presumed, square
35                                         Each chaotrope induces dissociation of five subunits in a con
36 onization of the peptides (e.g., detergents, chaotropes, inorganic salts).
37                                      Using a chaotrope-insoluble digestion method and quantitative cr
38  with respect to denaturation by heat and by chaotropes is presented.
39  indirect mechanism, in which urea acts as a chaotrope, is not a likely cause of urea's action as a d
40 LAP was refolded to its dimeric form using a chaotrope-mediated folding procedure.
41 reatment at alkaline pH ( > or = 10) or with chaotropes (NaBr, Nal, and urea), suggesting that these
42 of the effects of pressure, temperature, and chaotrope on unfolding of rhGH documented that under con
43 e surfactants, two organic solvents, and two chaotropes on the enzymatic digestion efficiency of memb
44 he adsorption and electrostatic repulsion of chaotropes on the hydrophobic portion of the membrane.
45 kosmotrope and sodium thiocyanate (NaSCN) as chaotrope, on BSA/lutein binding at pH 7.4 using fluores
46 ples of chao-/kosmotropicity values are, for chaotropes: phenol +143, CaCl(2) +92.2, MgCl(2) +54.0, b
47   In combination, these results suggest that chaotropes primarily induce protein solubilization by di
48 f-denaturation and upon the concentration of chaotrope required to half-denature the tracer at consta
49                  The addition of the charged chaotrope SCN(-) in 150 mM concentration improves the re
50                         We conclude that the chaotrope sensitivity of antibody binding to Env depends
51 substances (including potentially inhibitory chaotropes such as MgCl(2) and perchlorates) cannot acce
52 ants, either in buffer or in the presence of chaotropes such as thiocyanate, establish the presence o
53  of cell lysates with high concentrations of chaotropes such as urea.
54 antibody binding to Env antigens by an added chaotrope (such as thiocyanate).
55 ssment was possible without the use of added chaotropes, such as urea, to dissociate GroEL.
56  these data, we suggest that dilution of the chaotrope to initiate refolding will result in collapse
57 uanidine HCl and refolded by dilution of the chaotrope to minimally denaturing conditions and disulfi
58 tes assayed (from +361 kJ kg(-1) mol(-1) for chaotropes to -659 kJ kg(-1) mol(-1) for kosmotropes) bu
59                                              Chaotrope treatment of the paired grana membranes has al
60 ctural epitopes is particularly sensitive to chaotrope treatment, whereas antibody binding to epitope
61 lpy and entropy changes of this prototypical chaotrope were both determined to be negative.