1 Docked structures were consistent with
calorimetric analyses against bacterial beta-lactamases.
2 anistic studies by mutational and isothermal
calorimetric analyses allowed the design of RelA-mutants
3 Bioinformatic and
calorimetric analyses indicate that DnaA-box sequences i
4 However,
calorimetric analyses indicate very different thermodyna
5 onance spectroscopy and isothermal titration
calorimetric analyses of 10 of the inclusion complexes a
6 utant cycles (DMCs) coupled with kinetic and
calorimetric analyses of cognate Im9 and non-cognate Im2
7 Kinetic and
calorimetric analyses of site-specific replacement varia
8 Isothermal titration
calorimetric analyses of the purified YiiP and binding c
9 Isothermal titration
calorimetric analyses of the wild-type protein reveal th
10 and flap regions, and differential scanning
calorimetric analyses show that the mutation lowers the
11 Complementary, differential scanning
calorimetric analyses suggest that the two domains of VP
12 Here we report a
calorimetric analysis for the binding of a broad panel o
13 Calorimetric analysis of ARF7PB1 site-directed mutants d
14 Calorimetric analysis of several active site variants co
15 Isothermal titration
calorimetric analysis of the binding of (G202A)G alpha(i
16 Isothermal titration
calorimetric analysis of the comparative binding of Dyn2
17 Calorimetric analysis of the effect of active site mutat
18 Our isothermal titration
calorimetric analysis of the interaction between the GAB
19 Calorimetric analysis revealed that the enthalpy, rather
20 Calorimetric analysis showed that although these CBMs de
21 Calorimetric analysis shows that binding can occur first
22 crease in body weight or insulin resistance;
calorimetric analysis suggested an accelerated metabolis
23 Here we show by crystallographic, NMR, and
calorimetric analysis that the phosphotyrosine binding (
24 To examine these features, we used
calorimetric analysis to probe a possible ligand binding
25 supported both by molecular dynamics and by
calorimetric analysis.
26 Calorimetric and biochemical titrations indicate that th
27 the Syk kinase, we report a method combining
calorimetric and crystallographic measurements that reve
28 the (AATT)2 sequence was investigated using
calorimetric and equilibrium constant measurements.
29 dely useful and complementary alternative to
calorimetric and fluorescence measurements.
30 st this hypothesis, we used a combination of
calorimetric and fluorescence techniques.
31 Calorimetric and fluorescence titrations yielded binding
32 ermosensor, employing diverse spectroscopic,
calorimetric and hydrodynamic measurements.
33 and caspase 9 activities were measured with
calorimetric and luminescent assays in retinal extracts
34 That allowed prediction of the
calorimetric and mechanical glass transition temperature
35 Isothermal titration
calorimetric and molecular modeling data conformed to th
36 standing the binding mechanism, we performed
calorimetric and NMR titrations of several hnRNP A1 subd
37 comparison of simulated crystallinities with
calorimetric and optical measurements strongly suggests
38 arious DNA recognition sequences using micro-
calorimetric and optical methods.
39 The
calorimetric and quartz crystal microbalance data indica
40 n defect-free P3HT, as elucidated by various
calorimetric and scattering experiments, allow the devel
41 Calorimetric and spectroscopic characterizations of defe
42 Site-directed mutagenesis coupled with
calorimetric and spectroscopic data has been used to cha
43 Calorimetric and spectroscopic investigations of these t
44 ic bisquinolinium ligands, were monitored by
calorimetric and spectroscopic methods and by gel electr
45 d non-native forms of TNF-alpha by employing
calorimetric and spectroscopic methods.
46 In this study, we use
calorimetric and spectroscopic observables to detect, re
47 In the present work, we apply
calorimetric and spectroscopic techniques to a series of
48 Here we report results from
calorimetric and stress relaxation experiments using a 2
49 For Ac-(Gly-4(R)Hyp-4(R)Hyp)(10)-NH(2), the
calorimetric and the van't Hoff transition enthalpy Delt
50 We have made these measurements using
calorimetric and ultraviolet hypochromicity methods, as
51 e show that there is no reason to expect the
calorimetric and van't Hoff DeltaH degrees to be differe
52 DeltaH degrees and DeltaC(p), obtained from
calorimetric and van't Hoff methods.
53 was investigated by 1H NMR spectroscopy and
calorimetric and voltammetric techniques.
54 l/mol) have been measured in acetonitrile by
calorimetric and/or equilibrium methods.
55 Complementary adsorption,
calorimetric,
and infrared studies of the probe adsorbat
56 lished through a combination of biochemical,
calorimetric,
and spectroscopic techniques.
57 In recognition of this need, a
calorimetric-
and NMR-based approach for obtaining the r
58 The mystery surrounding this
calorimetric anomaly is epitomized by four decades long
59 A
calorimetric approach was used to characterize PPARgamma
60 Furthermore, using a new
calorimetric assay to accurately determine the temperatu
61 Calorimetric assessment of binding thermodynamics for he
62 energy expenditure, as measured by indirect
calorimetric assessment.
63 Calorimetric binding analysis indicated that Asp49 and A
64 Calorimetric binding analysis of residues in the c-di-GM
65 the basis of a thermostability shift assay,
calorimetric binding data, and biochemical assays which
66 -Fc complex and conduct isothermal titration
calorimetric binding studies.
67 In this report, a paper-based micro-
calorimetric biochemical detection method is presented.
68 Indirect
calorimetric canopy tests showed significant reductions
69 g structural data with observed spectral and
calorimetric changes, we now show that NusA binding dest
70 Calorimetric characterization of the association energet
71 Correlation of the
calorimetric,
circular dichroism, fluorescence, turbidit
72 The
calorimetric competition assay introduced here overcomes
73 phobic high-affinity ligands employing a new
calorimetric competition experiment is described.
74 Results from
calorimetric,
crystallographic, and theoretical analyses
75 t dielectric data and heating-rate-dependent
calorimetric data allow us to construct the relaxation m
76 Calorimetric data also shows that the membrane-proximal
77 The new
calorimetric data are consistent with all previously pub
78 Our fluorescence, absorbance, and
calorimetric data are consistent with loop migration/tra
79 Spectroscopic and
calorimetric data are consistent with two-state unfoldin
80 The
calorimetric data confirm the presence of at least two e
81 Calorimetric data confirmed that YkoF binds two thiamin
82 Calorimetric data indicate that M-CSF cannot dimerize FM
83 g site in each monomer, crystallographic and
calorimetric data indicate that VcFadR has two.
84 By applying a statistical model to
calorimetric data obtained on solvent mixtures, we show
85 Previously published
calorimetric data of a closely related bacteriophage, P2
86 Using
calorimetric data on surface energies for cobalt, iron,
87 n hydrophobic effect, in accord with earlier
calorimetric data on the membrane partition of other amp
88 s, which uses simulated annealing of complex
calorimetric data representing multiple coupled equilibr
89 Subtraction of buffer contributions to the
calorimetric data reveals that all three peptides have a
90 epresented by the Langmuir model; therefore,
calorimetric data should be used to extract thermodynami
91 Calorimetric data show that binding of pTppAp to RNase A
92 The (45)Ca binding and isothermal titration
calorimetric data show that myristoylation increases the
93 Calorimetric data show that this is due to proton-based
94 SbCOMT steady-state kinetic and
calorimetric data suggest a random bi-bi mechanism.
95 er a range of ionic strengths, combined with
calorimetric data, allowed separation of the electrostat
96 cture of this trapped complex, together with
calorimetric data, identifies sites of protein-protein i
97 For lipids lacking
calorimetric data, measurement of the critical micelle c
98 lent agreement with previous mutagenesis and
calorimetric data, providing the basis for further inves
99 Considering the
calorimetric data, substrate binding of SbHCT should occ
100 dues, coupled with available mutagenesis and
calorimetric data, suggest that subtle structural pertur
101 To aid interpretation of the
calorimetric data, the first crystal structure of a smal
102 The results are benchmarked against solution
calorimetric data.
103 ptide binding was recently proposed based on
calorimetric data.
104 We introduce the
calorimetric descriptor "metabolic capacity" and show th
105 monstrate the feasibility of integrating the
calorimetric detection method with paper based microflui
106 Calorimetric detection of biochemical reactions is demon
107 lpy arrays enable label-free, solution-based
calorimetric detection of molecular interactions in a 96
108 lpy arrays enable label-free, solution-based
calorimetric detection of molecular interactions in a 96
109 The
calorimetric detection results of DNA concentrations fro
110 We present here a
calorimetric determination of the field-temperature phas
111 Microfabricated
calorimetric devices are promising, although they have y
112 ling small samples and attaching them to the
calorimetric devices have been developed.
113 correlation of inhibitor chemistry with the
calorimetric dissection of thermodynamics.
114 Differential scanning
calorimetric (
DSC) analysis of the ADC indicated that th
115 (PI-5P)) mixed vesicles were investigated by
calorimetric (
DSC) Fourier transform infrared spectrosco
116 Spectroscopic experiments agreed well with
calorimetric (
DSC).
117 mprehensive global thermodynamic analysis of
calorimetric (
DSC, ITC) and spectroscopic (CD) data obta
118 eaks corresponding to dissociation of water (
calorimetric effect of 536Jg(-1) for beta-cyclodextrin a
119 ing with increased unfolding temperature and
calorimetric enthalpy as compared to pH 7.4.
120 -2.6 kcal/mol solution (toluene or C(6)D(6))
calorimetric enthalpy for the 2S/2SH tautomerization fav
121 A 50% decrease in
calorimetric enthalpy is observed, which may result from
122 folding was estimated from the dependence of
calorimetric enthalpy on T(m).
123 erence is that for gp120-B the van't Hoff to
calorimetric enthalpy ratio (DeltaH(vH)/DeltaH) is 0.95
124 mperature was lowered by 6 degrees C and the
calorimetric enthalpy reduced by 50% following removal o
125 iction, a significant decrease in stability,
calorimetric enthalpy, and folding time was observed for
126 roximately 2 degrees C) and no change in the
calorimetric enthalpy.
127 The
calorimetric entropy of the olivine-spinel transition in
128 These structures, complemented by
calorimetric equilibrium binding studies of MtDnaA DBD i
129 Here, we present direct
calorimetric evidence that no such enthalpic effects exi
130 , which is confirmed by isothermal titration
calorimetric experiment carried out in solution.
131 Global regression analysis of
calorimetric experiments at various concentrations and t
132 Temperature-dependent
calorimetric experiments give a DeltaC(p) for ligand bin
133 Biosensor and
calorimetric experiments indicate that the binding affin
134 on agree with results obtained from separate
calorimetric experiments on the Ca(2+)-ATPase derived fr
135 The results of isothermal-titration-
calorimetric experiments show that both lipophilic bisph
136 We performed spectroscopic and
calorimetric experiments to explore the folding kinetics
137 denaturation data from differential scanning
calorimetric experiments, and temperature and denaturant
138 The structure, combined with
calorimetric experiments, suggests distinct roles of thr
139 rotein was subjected to isothermal titration
calorimetric experiments.
140 t upon binding, determined from the scanning
calorimetric experiments.
141 tive volume, and chemical calibration of the
calorimetric factor used to convert the measured electri
142 ation calorimeters require validation of the
calorimetric factor with chemical reactions with accurat
143 stent with the previous isothermal titration
calorimetric finding that their interactions are entropy
144 approach to the fabrication of micromachined
calorimetric gas sensors for combustible gases.
145 The occurrence of water's
calorimetric glass transition of low-density amorphous i
146 ous ice at ambient pressure shows a distinct
calorimetric glass transitions at 116 K and present evid
147 The
calorimetric glucose detection demonstrates a measuremen
148 M NaCl causes low-temperature shifts in the
calorimetric HDL transitions of up to -14 degrees C.
149 ts by approximately -18 degrees C in the two
calorimetric HDL transitions without altering their natu
150 by magnetic nanoparticles is estimated from
calorimetric heating measurements.
151 In this study, we employ
calorimetric [
isothermal titration calorimetry (ITC) and
152 Calorimetric (
ITC) data also show that the overall entha
153 on resonance (SPR), and isothermal titration
calorimetric (
ITC) experiments with DB613, which has a c
154 also evaluated based on isothermal titration
calorimetric (
ITC) studies.
155 Also studied by
calorimetric,
kinetic, and in one case variable-temperat
156 fications in the DSC profiles might serve as
calorimetric markers when no monoclonal proteins can be
157 ers (T(m), DeltaH) as determined from direct
calorimetric means should be identical to those determin
158 Using direct
calorimetric measurement of heats of formation, MAPbI3 i
159 s this distortion, with the earlier reported
calorimetric measurement of the enthalpy gain of the K s
160 Isothermal titration
calorimetric measurements also showed an enthalpic contr
161 Calorimetric measurements and HSQC NMR spectra confirm t
162 t reaction enthalpies in good agreement with
calorimetric measurements and isotherms.
163 This evidence includes isothermal
calorimetric measurements and pH-jump experiments that s
164 tion are obtained from differential scanning
calorimetric measurements and thermal gravimetric analys
165 Systematic
calorimetric measurements are shown to provide a framewo
166 ined in spectroscopic, crystallographic, and
calorimetric measurements during early stages of insulin
167 ted Z-scores agree with estimates made using
calorimetric measurements for a few RNA molecules.
168 Instead,
calorimetric measurements have shown that the amorphous
169 Solution
calorimetric measurements in hexane show that the enthal
170 Calorimetric measurements indicate that RNase Sa has a h
171 Results of the
calorimetric measurements indicate that strong effector
172 asurements on crystals of d-ribose and other
calorimetric measurements make it possible to calculate
173 Calorimetric measurements of ATP binding to wild-type an
174 Calorimetric measurements of Ca and Li adsorption energi
175 Direct
calorimetric measurements of cognate telomeric ssDNA bin
176 Direct
calorimetric measurements of folding of a model host pep
177 Calorimetric measurements of metal adsorption energies d
178 ium oxide surfaces, determined from previous
calorimetric measurements of metal adsorption energies,
179 We report
calorimetric measurements of the heats of formation of c
180 is absent in liposomes and not detectable in
calorimetric measurements on liposome suspensions.
181 Differential scanning
calorimetric measurements on POPE/POPC liposomes with in
182 Here we report magnetic and
calorimetric measurements on YbRh2Si2, down to temperatu
183 Calorimetric measurements quantitatively confirm the ent
184 The
calorimetric measurements reveal that the bcc superlatti
185 duces the affinity for desmosomal cadherins,
calorimetric measurements show no significant effects of
186 Calorimetric measurements show that the change in enthal
187 Differential scanning
calorimetric measurements showed that s3 gains thermal s
188 Isothermal titration
calorimetric measurements suggest these complexes to be
189 has a ligand titration profile in isothermal
calorimetric measurements that clearly shows that one nu
190 emonstrate through mobility shift assays and
calorimetric measurements that the SU(VAR)3-9 HOMOLOG 5
191 etic isotope effect measurements, isothermal
calorimetric measurements, and (31)P NMR spectroscopic t
192 In the present work, vibration spectroscopy,
calorimetric measurements, and density functional theory
193 istochemistry of intestinal mucosa, indirect
calorimetric measurements, whole-body composition, and e
194 for ferric ion binding were determined from
calorimetric measurements.
195 = 60 +/- 10 cal/mol K bp, in agreement with
calorimetric measurements.
196 ort it by molecular dynamics simulations and
calorimetric measurements.
197 have developed a nanoparticle-based scanning
calorimetric method for the highly sensitive detections
198 This
calorimetric methodology provides a much more accurate a
199 Calorimetric methods are often used to determine enthalp
200 Considering that
calorimetric methods cannot distinguish between energeti
201 Calorimetric methods have been used to determine equilib
202 ed forms of Fet3p by using spectroscopic and
calorimetric methods in vitro (pH 7).
203 We show using isothermal
calorimetric methods that NbSyn2 binds specifically to m
204 ilar to values obtained by spectroscopic and
calorimetric methods with the additional confidence offe
205 iques, such as scattering, spectroscopic and
calorimetric methods, are not well adapted for their stu
206 red in acetonitrile by either equilibrium or
calorimetric methods.
207 ) with custom-fabricated picowatt-resolution
calorimetric microdevices, we created an experimental pl
208 use site-specific mutagenesis, coupled with
calorimetric,
NMR, and enzymological techniques, to defi
209 n a previously unidentified high-temperature
calorimetric peak.
210 are able to describe experimentally observed
calorimetric profiles and predict the anesthetic feature
211 on temperature of the main transition in the
calorimetric profiles and the shape similarity criterion
212 t common molecular markers contribute to the
calorimetric profiles of the different, secretory and no
213 ed that 4-MB exhibits a dual ratiometric and
calorimetric response toward peroxynitrite due to ONOO(-
214 The
calorimetric results argue that, from a thermodynamics p
215 Based on the
calorimetric results for 12 peptides, it was found that
216 e plasmon resonance and isothermal titration
calorimetric results indicate that the compound binds wi
217 Below 30 degrees C the
calorimetric results show that apoA-I interaction with P
218 The computational and
calorimetric results were in excellent agreement.
219 tubulin was found to be consistent with the
calorimetric results.
220 bon binding to P450 2A6, as evidenced by the
calorimetric results.
221 ovel, custom-fabricated, picowatt-resolution
calorimetric scanning probes, we measured the thermal co
222 oach integrates microfabricated differential
calorimetric sensors with microfluidic titration.
223 ly by Mossbauer spectroscopy, is seen in the
calorimetric signal.
224 this connection, DeltaC(p) provides a useful
calorimetric signature for assessing the relative impact
225 d controversially for many years because its
calorimetric signature is very feeble.
226 The
calorimetric signature of the second glass transition is
227 We also report agglutination and
calorimetric solution-phase binding studies of mono- and
228 e and sensitive nanomechanical infrared (IR)
calorimetric spectrometer for use in the direct detectio
229 uption of spherical HDL in 0-15% PEG-8000 by
calorimetric,
spectroscopic, electron microscopic, and l
230 eous modeling of orthogonal observables from
calorimetric,
spectroscopic, hydrodynamic, biosensing, o
231 the Rab11 GTPase using isothermal titration
calorimetric studies and mutational analysis.
232 Calorimetric studies demonstrate that this mutation faci
233 Calorimetric studies demonstrated these PDCs to be therm
234 ost promising stereoisomer (S)-16, X-ray and
calorimetric studies in PPARgamma revealed, at high liga
235 Calorimetric studies in which binding of 2',5'-ADP to CP
236 In fact,
calorimetric studies indicate that CD38-deficient animal
237 Calorimetric studies indicate that the increased stabili
238 +) should be purely enthalpic in accord with
calorimetric studies of a high-affinity consensus peptid
239 Isothermal titration
calorimetric studies of Co(2+) and Zn(2+) binding to EaC
240 Recent
calorimetric studies of interactions between small molec
241 Computational and
calorimetric studies of the anhydrous calcium phases, [C
242 Calorimetric studies of the binding of IscU mutants to t
243 Here we report isothermal titration
calorimetric studies of the effects of selectivity-modif
244 Isothermal titration
calorimetric studies of these lipid A derivatives with p
245 Both structural and
calorimetric studies point to a structural role for the
246 Calorimetric studies reveal that NC destabilization is e
247 Calorimetric studies revealed that binding of f-ImPyIm,
248 es) = -52 +/- 5 cal mol(-1) K(-1).) Solution
calorimetric studies show that the enthalpy of formation
249 FMN dimers in solution, isothermal titration
calorimetric studies show that these dimers bind strongl
250 We further use structural and
calorimetric studies to demonstrate that the end product
251 ger-finger interactions are observed also in
calorimetric studies, in which the 160(+/-20)nM (zf1) an
252 Calorimetric studies, including a novel ITC compound dis
253 ompared through biochemical, structural, and
calorimetric studies, showing a complex interplay betwee
254 stallography, site-directed mutagenesis, and
calorimetric studies, we have characterized the interact
255 entropies relative to free energies in some
calorimetric studies.
256 as demonstrated by thermal-shift, AS-MS, and
calorimetric studies.
257 hermal denaturation and isothermal titration
calorimetric studies.
258 from the results of the isothermal titration
calorimetric studies.
259 usly detected by circular dichroism (CD) and
calorimetric studies.
260 ugh multiple cyclic mixed-gas adsorption and
calorimetric studies.
261 An isothermal titration
calorimetric study of the binding of substrates and inhi
262 Traditionally, a variety of
calorimetric techniques and in situ XRD at elevated temp
263 Calorimetric techniques have demonstrated that although
264 We use spectroscopic and
calorimetric techniques to characterize the binding of t
265 y, we use a combination of spectroscopic and
calorimetric techniques to detect and characterize kinet
266 We used a combination of spectroscopic and
calorimetric techniques to determine complete thermodyna
267 k, we have used a combination of optical and
calorimetric techniques to determine thermodynamic unfol
268 DtxR(M10A,C102D) using crystallographic and
calorimetric techniques to gain insight into the possibl
269 We used a combination of spectroscopic and
calorimetric techniques to investigate the folding/unfol
270 We used a combination of optical and
calorimetric techniques to investigate the incorporation
271 This study applies NMR and
calorimetric techniques to map the binding site for Rem2
272 , we used a combination of spectroscopic and
calorimetric techniques to present a complete thermodyna
273 resting KatG was examined using optical and
calorimetric techniques to provide thermodynamic paramet
274 A combination of spectroscopic and
calorimetric techniques was used to determine complete t
275 Spectroscopic and
calorimetric techniques were employed to characterize an
276 ining ionic liquids, measured directly using
calorimetric techniques, is presented in this paper.
277 oscopic, light scattering, fluorescence, and
calorimetric techniques, the precise details of the ener
278 othermal titration and differential scanning
calorimetric techniques.
279 (Tg-10 degrees C), previously determined by
calorimetric tests.
280 New endothermic peaks in the
calorimetric thermograms of treated milk revealed the fo
281 d by combination of isotherms from different
calorimetric titration experiments into a global analysi
282 Isothermal
calorimetric titration of LIGHT with either LTbetaR or L
283 Isothermal
calorimetric titration of MutT with 8-oxo-dGMP yields a
284 Calorimetric titration shows that the RNA sequence 5'AGC
285 ty binding site of DtxR(E175K) obtained from
calorimetric titration with Ni(II) is K(a)=7.6+/-0.5x10(
286 he TSIL with U was carried out by isothermal
calorimetric titration, liquid-liquid extraction, (31)P
287 Calorimetric titrations in different buffers and pH cond
288 NMR and isothermal
calorimetric titrations of N-betaGRP with laminarihexaos
289 affinities for metal ion extracted from the
calorimetric titrations of the mutants DtxR(D6A,C102D) a
290 Calorimetric titrations of the syn isomer with bromide c
291 Calorimetric titrations result in one-to-one binding als
292 Calorimetric titrations show that the ferroxidase center
293 We have conducted isothermal
calorimetric titrations to investigate the halogen-bond
294 Calorimetric titrations using monomeric enzyme yielded a
295 showed no detectable change in Fe2+ and Hg2+
calorimetric titrations, indicating that Asp-157 is not
296 Here we report a combination of isothermal
calorimetric titrations, NMR spectroscopy, and extensive
297 ges observed in the SANS measurements, and a
calorimetric transition enthalpy of 60 +/- 3 kJ mol(-1)
298 The first
calorimetric transition reflects HDL fusion and dissocia
299 ils is located at temperatures far below the
calorimetric transition.
300 , with good agreement between van't Hoff and
calorimetric values.