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