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1 dine rings into a left-handed (M) propeller (circular dichroism spectroscopy).
2 ase with BA was measured by fluorescence and circular dichroism spectroscopy.
3 icelles and small unilamellar vesicles using circular dichroism spectroscopy.
4 metry, isothermal titration calorimetry, and circular dichroism spectroscopy.
5 a-helical (alahel) peptides were measured by circular dichroism spectroscopy.
6 d with differential scanning calorimetry and circular dichroism spectroscopy.
7 ine II (PPII)-like conformation, as shown by circular dichroism spectroscopy.
8 rophores was examined using fluorescence and circular dichroism spectroscopy.
9 Fourier transform infrared spectroscopy, and circular dichroism spectroscopy.
10 erized by UV-visible absorption and magnetic circular dichroism spectroscopy.
11 tigated by thermal denaturation monitored by circular dichroism spectroscopy.
12 cal and 10.3% beta-strand structure based on circular dichroism spectroscopy.
13 formation of the DNA duplex as determined by circular dichroism spectroscopy.
14 sing the osmotic stress method combined with circular dichroism spectroscopy.
15 omers, respectively, based on proton NMR and circular dichroism spectroscopy.
16 ge degree of helicity in C52L as measured by circular dichroism spectroscopy.
17 hysical methods such as fluorescence, UV and circular dichroism spectroscopy.
18 st Arrhenius analysis of HDL denaturation by circular dichroism spectroscopy.
19 red to the wild-type protein, as measured by circular dichroism spectroscopy.
20 substantial helical structure as measured by circular dichroism spectroscopy.
21 ndom coil secondary structure as measured by circular dichroism spectroscopy.
22 their triple helical nature was confirmed by circular dichroism spectroscopy.
23 ucture change was investigated using near-UV circular dichroism spectroscopy.
24 lix as judged by collagenase sensitivity and circular dichroism spectroscopy.
25 died by isothermal titration calorimetry and circular dichroism spectroscopy.
26 flow small-angle X-ray scattering and far-UV circular dichroism spectroscopy.
27 were studied via UV thermal denaturation and circular dichroism spectroscopy.
28 ure-dependent unfolding is then monitored by circular dichroism spectroscopy.
29 olding characteristics assessed using far-UV circular dichroism spectroscopy.
30 lectrospray ionization mass spectrometry and circular dichroism spectroscopy.
31   Three, the cluster chirality was gauged by circular dichroism spectroscopy.
32 verlap, to form complexes was analyzed using circular dichroism spectroscopy.
33 ir spaced three or four residues apart using circular dichroism spectroscopy.
34 ike DNA:RNA heteroduplexes when analyzed via circular dichroism spectroscopy.
35 bserved during fibril formation using far-UV circular dichroism spectroscopy.
36 e fluorescence, fluorescence anisotropy, and circular dichroism spectroscopy.
37 tivity of our TPA methodology is compared to circular dichroism spectroscopy.
38 ectron-electron resonance, and high-pressure circular dichroism spectroscopy.
39 ondary protein structure, as demonstrated by circular dichroism spectroscopy.
40 their nanoring hosts is evident from NMR and circular dichroism spectroscopy.
41  Fourier transform infrared spectroscopy and circular dichroism spectroscopy.
42 at is typically detectable with conventional circular dichroism spectroscopy.
43 this supramolecular polymer was confirmed by circular dichroism spectroscopy.
44  using differential scanning calorimetry and circular dichroism spectroscopy.
45 eparated by chiral HPLC and characterized by circular dichroism spectroscopy.
46 enaturation, native gel electrophoresis, and circular dichroism spectroscopy.
47 h 2 and Ara h 3), digestion experiments, and circular dichroism spectroscopy.
48 different lipid mixtures was investigated by circular dichroism spectroscopy.
49  mass spectrometry (DT IM-MS) in addition to circular dichroism spectroscopy.
50 ional ensemble, which is supported by far-UV circular dichroism spectroscopy.
51 l intermediates that has come primarily from circular dichroism spectroscopy.
52 intrinsic tryptophan fluorescence as well as circular dichroism spectroscopy.
53  absorption, photoluminescence, and magnetic circular dichroism spectroscopies.
54 have been characterized using UV-visible and circular dichroism spectroscopies.
55 tein structural changes than fluorescence or circular dichroism spectroscopies.
56  (DSC), fluorescence-quenching, infrared and circular dichroism spectroscopies.
57 induced denaturation, using fluorescence and circular dichroism spectroscopies.
58 by Fourier transform IR, NMR, and electronic circular dichroism spectroscopies.
59                        These were studied by circular dichroism spectroscopy, a variety of Fourier tr
60 r were monitored with time-resolved magnetic circular dichroism spectroscopy after photodissociation
61                                              Circular dichroism spectroscopy also indicates that the
62                                       Far UV circular dichroism spectroscopy analyses of lipid-bound
63                                              Circular dichroism spectroscopy, analytical ultracentrif
64 se two sets of artificial helices by NMR and circular dichroism spectroscopies and find that the hydr
65 asurements) with PPII structure (as shown by circular dichroism spectroscopy and (3)J(HN-C alpha) con
66                                              Circular dichroism spectroscopy and 2-aminopurine (2AP)
67                                        Using circular dichroism spectroscopy and ab initio calculatio
68                                              Circular dichroism spectroscopy and amide exchange exper
69 ated the detailed nature of this dimer using circular dichroism spectroscopy and analytical ultracent
70 1-131, 1-260 and 1-284) and characterized by circular dichroism spectroscopy and analytical ultracent
71 f the alpha-helical domains are confirmed by circular dichroism spectroscopy and by rheological measu
72 de gel electrophoresis, and fluorescence and circular dichroism spectroscopy and compared with those
73 d by measuring the temperature dependence by circular dichroism spectroscopy and confirmed by differe
74             We characterized the peptides by circular dichroism spectroscopy and determined high-reso
75 nd cancer kinase mutants are consistent with circular dichroism spectroscopy and differential scannin
76                                              Circular dichroism spectroscopy and differential scannin
77 nt proteins, as experimentally determined by circular dichroism spectroscopy and differential scannin
78 he photosynthetic complexes, as evidenced by circular dichroism spectroscopy and differential scannin
79                                        Using circular dichroism spectroscopy and differential scannin
80                                              Circular dichroism spectroscopy and dynamic light scatte
81 de interactions in hydrophobic milieus using circular dichroism spectroscopy and Forster resonance en
82 tertiary structure, which were determined by circular dichroism spectroscopy and gel electrophoresis,
83                                              Circular dichroism spectroscopy and gel filtration studi
84 he ankyrin-B C-terminal domain determined by circular dichroism spectroscopy and hydrodynamic paramet
85 nt proportion of the change measured by both circular dichroism spectroscopy and interfacial methods
86  EHMT1 p.P809L was also studied using far UV circular dichroism spectroscopy and intrinsic protein fl
87                                      We used circular dichroism spectroscopy and isothermal titration
88 re or subunit association state, as shown by circular dichroism spectroscopy and light-scattering pho
89                                              Circular dichroism spectroscopy and limited proteolysis
90                               In addition to circular dichroism spectroscopy and limited proteolysis,
91      Examining the unfolding of rhodopsin by circular dichroism spectroscopy and measuring the rate o
92                                              Circular dichroism spectroscopy and molecular dynamics s
93 P and unable to autoprocess were analyzed by circular dichroism spectroscopy and multi-angle laser li
94                                              Circular dichroism spectroscopy and nuclear magnetic res
95            Through a combination of magnetic circular dichroism spectroscopy and potentiometric titra
96                              On the basis of circular dichroism spectroscopy and reactivity with thio
97  in the pH range of 7.5-3.0 are monitored by circular dichroism spectroscopy and site-directed trypto
98         Secondary structure determination by circular dichroism spectroscopy and structure modeling a
99                                              Circular dichroism spectroscopy and thermal stability st
100  Data from powder X-ray diffraction, UV, and circular dichroism spectroscopy and ThT fluorescence ind
101 II)-like helix conformation when examined by circular dichroism spectroscopy and were monomers as jud
102                                              Circular-dichroism spectroscopy and nuclear magnetic res
103 opy, electronic absorption spectroscopy, and circular dichroism spectroscopy) and computational techn
104 red by differential scanning calorimetry and circular dichroism spectroscopy) and urea-induced unfold
105 aracterized by analytical gel filtration and circular dichroism spectroscopy, and activity was assess
106 n lacks detectable secondary structure using circular dichroism spectroscopy, and demonstrate that fi
107 f less than 50 mug using microcryoprobe NMR, circular dichroism spectroscopy, and density functional
108 spectrometry, size-exclusion chromatography, circular dichroism spectroscopy, and electron microscopy
109 drogen/deuterium exchange mass spectrometry, circular dichroism spectroscopy, and enzymatic digestion
110   This designed protein was characterized by circular dichroism spectroscopy, and found to have secon
111      We have used fluorescence spectroscopy, circular dichroism spectroscopy, and gel electrophoresis
112 ange mass spectrometry, limited proteolysis, circular dichroism spectroscopy, and gel filtration chro
113 ty to form six-helix bundles was examined by circular dichroism spectroscopy, and HIV/SIV Env-mediate
114 e-directed mutagenesis, phage plaque assays, circular dichroism spectroscopy, and in vitro genome eje
115 ure differences, Mossbauer spectra, magnetic circular dichroism spectroscopy, and integer-spin EPR sp
116 mined with calorimetry, electron microscopy, circular dichroism spectroscopy, and internal reflection
117 resonance assay combined with absorbance and circular dichroism spectroscopy, and kinetics analysis o
118            Thioflavin T fluorescence assays, circular dichroism spectroscopy, and one-dimensional pro
119 ared and characterized using metal analyses, circular dichroism spectroscopy, and presteady-state and
120 sequence, were synthesized, characterized by circular dichroism spectroscopy, and tested for IgE reac
121  both peptides, similar to those obtained by circular dichroism spectroscopy, and the Fourier transfo
122 onstants could be evaluated by time-resolved circular dichroism spectroscopy, and the results could h
123 re monitored via intrinsic Trp fluorescence, circular dichroism spectroscopy, and transmission electr
124 udies by using dot blotting, immunoblotting, circular dichroism spectroscopy, and transmission electr
125  this work isothermal titration calorimetry, circular dichroism spectroscopy, and two-photon microsco
126 ably folded conformation, as demonstrated by circular dichroism spectroscopy, and undergoes a transit
127                                              Circular dichroism spectroscopy applied to peptides corr
128 H acylation analyzed by primer extension and circular dichroism spectroscopy are consistent with our
129  unfolded state was revealed with the aid of circular dichroism spectroscopy as a function of denatur
130 fs include absorption, emission, linear, and circular dichroism spectroscopies, as well as viscometry
131                                           By circular dichroism spectroscopy, atomic force microscopy
132               It is shown that, according to circular dichroism spectroscopy, both the 1',4'-iminopyr
133  series of host peptides was monitored using circular dichroism spectroscopy (CD) and differential sc
134 and BCA-Ac(18) are catalytically active, and circular dichroism spectroscopy (CD) suggests that they
135 d UV resonance Raman spectroscopy (UVRR) and circular dichroism spectroscopy (CD) to monitor the back
136                      Supporting data include circular dichroism spectroscopy (CD), NMR spectroscopy,
137 ere also investigated through application of Circular Dichroism spectroscopy (CD).
138                                 In addition, circular dichroism spectroscopy clearly demonstrated tha
139                        Synchrotron radiation circular dichroism spectroscopy confirmed that purified
140 econdary structure of BBA74 as determined by circular dichroism spectroscopy consists of at least 78%
141 es compared to Abeta (1-42), as indicated by circular dichroism spectroscopy data.
142  microscopy, ThT fluorescence assays, far-UV circular dichroism spectroscopy, deep-UV resonance Raman
143                                              Circular dichroism spectroscopy demonstrated different s
144               Thermal stability monitored by circular dichroism spectroscopy demonstrated that both c
145                                              Circular dichroism spectroscopy demonstrated that in the
146 ination of gel-filtration chromatography and circular dichroism spectroscopy demonstrated that recomb
147 structural content of core RAG1, obtained by circular dichroism spectroscopy, demonstrated a signific
148 erium exchange mass spectrometry, as well as circular dichroism spectroscopy, demonstrated that the b
149                                              Circular dichroism spectroscopy demonstrates that peptid
150                                              Circular dichroism spectroscopy, differential scanning c
151                                        Using circular dichroism spectroscopy, differential scanning c
152                     UV-Visible spectroscopy, Circular Dichroism spectroscopy, Dynamic Light Scatterin
153 tween the NDI units probed by absorption and circular dichroism spectroscopies, electrochemistry and
154 sembles is supported by gel electrophoresis, circular dichroism spectroscopy, equilibrium analytical
155                                              Circular dichroism spectroscopy experiments show that th
156                                              Circular dichroism spectroscopy experiments showed that
157 are essentially unchanged, in agreement with circular dichroism spectroscopy experiments that show th
158    Gel-filtration, dynamic light scattering, circular dichroism spectroscopy, fluorescence spectrosco
159 ments with a new quantitative application of circular dichroism spectroscopy for determining the frac
160 organic and aqueous solvents) by vibrational circular dichroism spectroscopy for the first time.
161 g reflectance spectroscopy and by UV-vis and circular dichroism spectroscopy for the soluble protein
162 ined in detail using laser light scattering, circular dichroism spectroscopy, Fourier transform infra
163                                              Circular dichroism spectroscopy gave evidence that all o
164 fied recombinant forms of the two domains by circular dichroism spectroscopy, gel permeation chromato
165 e (EPR), electronic absorption, and magnetic circular dichroism spectroscopies have been performed on
166          NIR circular dichroism and magnetic circular dichroism spectroscopies have been used to prob
167 ethyl-Ni(III) species; furthermore, magnetic circular dichroism spectroscopy identified the Ni(II)-th
168                                              Circular dichroism spectroscopy in combination with dyna
169 ht scattering, stopped-flow fluorescence and circular dichroism spectroscopy in combination with ther
170 n building block was studied in detail using circular dichroism spectroscopy in the IR and UV/VIS fre
171 taredoxin in A. vinelandii, was monitored by circular dichroism spectroscopy, in the absence and in t
172                                    Data from circular dichroism spectroscopy indicate that base analo
173  a smaller lamellar repeat distance, whereas circular dichroism spectroscopy indicated a perturbed lo
174                                              Circular dichroism spectroscopy indicated that all DNA d
175                                              Circular dichroism spectroscopy indicated that all tripl
176                     Thermal denaturation and circular dichroism spectroscopy indicated that modificat
177                                 Results from circular dichroism spectroscopy indicated that no major
178                                              Circular dichroism spectroscopy indicated that the most
179                           Far-UV and near-UV circular dichroism spectroscopy indicated that there wer
180 urther analysis of both proteins with far-UV circular dichroism spectroscopy indicated that they were
181                                              Circular dichroism spectroscopy indicated that vortexing
182  and chemical denaturation experiments using circular dichroism spectroscopy indicated the overall st
183                                              Circular dichroism spectroscopy indicates that pyrvinium
184                                              Circular dichroism spectroscopy indicates unusual featur
185  with the full-length protein, using NMR and circular dichroism spectroscopy, indicates that the 14 C
186 ns were evaluated for secondary structure by circular dichroism spectroscopy, iron-binding by atomic
187                              Far ultraviolet circular dichroism spectroscopy is used to identify the
188 ored by steady state fluorescence and far-UV circular dichroism spectroscopy, is cooperative with no
189  a combination of fluorescence spectroscopy, circular dichroism spectroscopy, isothermal titration ca
190 es, including nuclear magnetic resonance and circular dichroism spectroscopy, isothermal titration ca
191  disordered, and using synchrotron radiation circular dichroism spectroscopy, its secondary structure
192 y disordered (natively unfolded) as shown by circular dichroism spectroscopy, lack of chemical-shift
193                                        Using circular dichroism spectroscopy, light scattering measur
194                              Here we show by circular dichroism spectroscopy, light scattering, isoth
195 g a combination of UV-visible absorbance and circular dichroism spectroscopy, limited proteolysis, an
196                                        Using circular dichroism spectroscopy, limited proteolysis, ki
197 electronic absorption spectroscopy, magnetic circular dichroism spectroscopy, magnetic susceptibility
198 ogenic transmission electron microscopy, and circular dichroism spectroscopy measurements were perfor
199 isodesmic model to (1)H NMR spectrometry and circular dichroism spectroscopy measurements.
200 cture-activity relationship study, including circular dichroism spectroscopy, minimum inhibitory conc
201 aracterized by melting temperature analysis, circular dichroism spectroscopy, native and denaturing p
202 ta-TM) for the two Tmod1 binding sites using circular dichroism spectroscopy, native gel electrophore
203 ity and conformation of 6-HBs as detected by circular dichroism spectroscopy, native polyacrylamide g
204                                              Circular dichroism spectroscopy, NMR, and computational
205                                              Circular dichroism spectroscopy, nuclear magnetic resona
206                                              Circular dichroism spectroscopy of alpha211 revealed a c
207                                       Far-UV circular dichroism spectroscopy of apoA-I-(44-186) in bu
208                                              Circular dichroism spectroscopy of p53 peptides shows th
209                                              Circular dichroism spectroscopy of purified peptides wit
210                                              Circular dichroism spectroscopy of the peptoids revealed
211                              Consistent with circular dichroism spectroscopy, our results showed no m
212                  Using various immunoassays, circular dichroism spectroscopy, photoinduced cross-link
213      Both forms of p17 were characterized by circular dichroism spectroscopy, protein chemical denatu
214 variable temperature/variable field magnetic circular dichroism spectroscopy, provide strong evidence
215 nal regions of ALF and TFIIAalpha/beta using circular dichroism spectroscopy provided the first evide
216  the protein, as measured by far and near-UV circular dichroism spectroscopy, respectively.
217 xylate-oxygen is an M(+) ligand, and EPR and circular dichroism spectroscopies reveal that both the s
218 ing UV/visible absorption, luminescence, and circular dichroism spectroscopies reveal, for the sexith
219 odimer, together with mutagenesis and far-UV circular dichroism spectroscopy, reveal its mechanisms f
220                                              Circular dichroism spectroscopy revealed a conformationa
221                        Consistent with this, circular dichroism spectroscopy revealed a stable, solub
222                                              Circular dichroism spectroscopy revealed an alpha-helica
223 d secondary structure predictions as well as circular dichroism spectroscopy revealed an alpha-helica
224                                              Circular dichroism spectroscopy revealed that BHBox show
225                                              Circular dichroism spectroscopy revealed that removal of
226 addition, secondary structure analysis using circular dichroism spectroscopy revealed that the C-term
227                   Ultraviolet absorption and circular dichroism spectroscopy revealed that the protei
228 a peptidase investigated by fluorescence and circular dichroism spectroscopy revealed that the protei
229                                       Far-UV circular dichroism spectroscopy revealed the peptide is
230  denaturation studies using fluorescence and circular dichroism spectroscopy show that each protein u
231                                              Circular dichroism spectroscopy showed a pH-dependent ch
232                               Interestingly, circular dichroism spectroscopy showed a similar helical
233 pologies between d- and l-enantiomers, which circular dichroism spectroscopy showed adopt mirror imag
234 rement of fibrillating glucagon using far-UV circular dichroism spectroscopy showed changes in struct
235                                              Circular dichroism spectroscopy showed no obvious thermo
236           Small angle neutron scattering and circular dichroism spectroscopy showed no substantial ch
237                                              Circular dichroism spectroscopy showed that both peptide
238                                              Circular dichroism spectroscopy showed that the non-nati
239 y of BTA moieties into helical aggregates by circular dichroism spectroscopy showed that the stabilit
240 icroscopy, small angle x-ray scattering, and circular dichroism spectroscopy, showing that it assumes
241                                              Circular dichroism spectroscopy shows no evidence for ex
242                                              Circular dichroism spectroscopy shows strong Cotton effe
243                                              Circular dichroism spectroscopy shows that IpgC binding
244                                              Circular dichroism spectroscopy shows that the Jun N-ter
245                                          The circular dichroism spectroscopy signatures for all three
246 is):B(Thr)](2) is provided by UV/visible and circular dichroism spectroscopies, size exclusion chroma
247  the structural and functional changes using circular dichroism spectroscopy, size exclusion chromato
248                                 Results from circular dichroism spectroscopy, size exclusion chromato
249 ers in the absence of detergent as judged by circular dichroism spectroscopy, size-exclusion chromato
250 btained using chemical and nuclease mapping, circular dichroism spectroscopy, small-angle X-ray scatt
251 double-stranded, coiled-coil, was studied by circular dichroism spectroscopy, spectrofluorimetry and
252                                              Circular dichroism spectroscopy studies and confocal mic
253                                              Circular dichroism spectroscopy studies on missense muta
254 ron microscopy, atomic force microscopy, and circular dichroism spectroscopy studies reveal that this
255 Using the NR1 C0 region for fluorescence and circular dichroism spectroscopy studies we found that no
256 atography, small-angle x ray scattering, and circular dichroism spectroscopy suggest partial unfoldin
257 ucture of the unbound protein as assessed by circular dichroism spectroscopy, suggesting that conform
258                                              Circular dichroism spectroscopy suggests that Tax(59-98)
259 optical needle has potential applications in circular dichroism spectroscopy, super-resolution imagin
260  on hydrogels, and on membranes by employing circular dichroism spectroscopy, surface plasmon resonan
261 s of RNA G-quadruplexes using UV melting and circular dichroism spectroscopy that also serves as a co
262 this aptamer in vitro, and demonstrate using circular dichroism spectroscopy that LJM-3064 undergoes
263           For comparison, we show by NMR and circular dichroism spectroscopy that the G7K mutant of c
264 tructure as determined by synchrotron far-UV circular dichroism spectroscopy; the most stable bicelle
265                                        Using circular dichroism spectroscopy, thermal stability was m
266         The new assembly is characterized by circular dichroism spectroscopy ([theta;](222) = -30 317
267 cts of these substitutions were probed using circular dichroism spectroscopy, thioflavin T binding, e
268 .1 (hSAA1.1) - using techniques ranging from circular dichroism spectroscopy to atomic force microsco
269 electron microscopy, ultracentrifugation and circular dichroism spectroscopy to be a 1.15 MDa tetrame
270  of enzymatic assays, PA-binding assays, and circular dichroism spectroscopy to evaluate the interact
271                   We employed UV melting and circular dichroism spectroscopy to examine and compare t
272           In this work, we utilized magnetic circular dichroism spectroscopy to explore how the elect
273 ultiscale molecular dynamics simulations and circular dichroism spectroscopy to explore the structure
274                       Aptamers were shown by circular dichroism spectroscopy to induce structural cha
275 -state intrinsic tryptophan fluorescence and circular dichroism spectroscopy to investigate the confo
276  temperature-dependent synchrotron radiation circular dichroism spectroscopy to measure half-denatura
277 e have used small-angle X-ray scattering and circular dichroism spectroscopy to measure the sigma of
278             We used multidimensional NMR and circular dichroism spectroscopy to monitor the observed
279             The method was complemented with circular dichroism spectroscopy, tryptophan fluorescence
280  d(CGCGAATTGCGC), and d(CGCAAATTTCGC), using circular dichroism spectroscopy, ultraviolet resonance R
281 econdary structural changes were detected by circular dichroism spectroscopy upon the addition of ves
282                                              Circular dichroism spectroscopy, used to monitor thermal
283                                       Far-UV circular dichroism spectroscopy was used to confirm the
284                                              Circular dichroism spectroscopy was used to directly mon
285                                              Circular dichroism spectroscopy was used to follow struc
286                                              Circular Dichroism spectroscopy was used to investigate
287                                              Circular dichroism spectroscopy was used to probe the se
288                                              Circular dichroism spectroscopy was used to show that th
289                        Using mutagenesis and circular dichroism spectroscopy we now demonstrate that
290                                        Using circular dichroism spectroscopy, we determined that the
291                  Using synchrotron radiation circular dichroism spectroscopy, we have determined that
292                                        Using circular dichroism spectroscopy, we have shown that not
293                                        Using circular dichroism spectroscopy, we measured the alpha h
294                                        Using circular dichroism spectroscopy, we show that alkylation
295                 Using non-degenerate optical circular dichroism spectroscopy, we show that charge tra
296                                        Using circular dichroism spectroscopy, we show that RIN4 is a
297                               UV/visible and circular dichroism spectroscopies were employed to detai
298          Electron paramagnetic resonance and circular dichroism spectroscopy were used to characteriz
299 ring the kinetics are to use fluorescence or circular dichroism spectroscopy, which do not uniquely r
300 ture of these mutant proteins as analyzed by circular-dichroism spectroscopy, which demonstrates that

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