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. (If this happens to you, contact the Council of Parent Attorneys and Advocates [copaa
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. Unfolding of GR by GdnHCl was further characterized by intrinsic fluorescence anisotropy measurements (Fig
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. Monoclonal antibody based immunoassay for human aminoacylase-1
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. Stated differently, con-elated chain repulsions drastically reduce the probability that the N- and C-termini come very close together
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. coelicolor, HPr^sup sc^, are different from those of the other members of the HPr family (17-19)
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. Depending on the kind of denaturing conditions (high salt concentrations, extreme pH, elevated temperatures, pressure, etc
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. The authors thank Jacques Colletier for useful discussions on cholinesterase biochemistry as well as the IN16 instrumental team (Bernhard Frick, Thilo Seydel, and Matthias Elender) and the IN13-CRG team (Marc Bée, Francesca Natali, and Sebastien Vial) at the Institute Laue-Langevin, Grenoble, France
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. Ca^sup 2+^ signaling can inhibit the transcriptional activities in vivo of the bHLH proteins E12 and SEF2-1 through direct binding of Ca^sup 2+^/CaM to the basic sequence of the proteins, resulting in inhibition of their DNA binding (15)
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. Temperature sensitive microgel suspensions: colloidal phase behavior and rheology of soft spheres
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. This produces unfolded monomeric TTR
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. ThT, on the other hand, requires a pH adjustment for its characteristic amyloid fluorescence signal (Fig
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. , 2002), it may be as well the different degrees of packing of protofilaments in the fibers' core and on its surface that evoke this effect
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. 3[degrees]C (March 1985) and 18
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. But it now appears that these expectations will not be met
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. Compact intermediate slates in protein folding
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. It may be therefore hypothesized that the protofilament structure gives rise to an inherent mechanical strain, which may be relaxed either by a collective twisting of associated protofilaments, or curling them
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. Since we use relative peak positions and distance (inter-arm proximity) changes in our discussion here (and not absolute distances), variations of [gamma] from 1 do not affect the discussion or conclusions of this study
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. We define this reference time as the average burst duration within the 0
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. These rates are much faster than the overall rate constant for ribozyme docking observed in previous ensemble kinetic studies, which is on the order of 10^sup -2^ s^sup -1^ for a 2WJ ribozyme construct (N
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. Energetics of hydrogen bond networks in RNA: Hydrogen bonds surrounding G+1 and U42 are the major determinants for the tertiary structure stability of the hairpin ribozyme
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