ライフサイエンスコーパス: CD spectroscopy

1 n behavior was confirmed by NMR, UV/vis, and CD spectroscopy.

2 nalysis combined with Br(2) footprinting and CD spectroscopy.

3 oenriched and monitoring its racemization by CD spectroscopy.

4 tigated by gel-filtration chromatography and CD spectroscopy.

5 ed by crystallography, Fe removal rates, and CD spectroscopy.

6 the gp120 molecule, as also demonstrated by CD spectroscopy.

7 pported by size-exclusion chromatography and CD spectroscopy.

8 ds, does it show a chiral excess measured by CD spectroscopy.

9 y structure of the proenzyme, as revealed by CD spectroscopy.

10 alpha-helix propensities varied as shown by CD spectroscopy.

11 n solution at pH 4.7-7.8 by far- and near-UV CD spectroscopy.

12 fully unfolded protein were investigated by CD spectroscopy.

13 /P50L as observed by both the cGMP assay and CD spectroscopy.

14 also a disturbed structure as determined by CD spectroscopy.

15 s of ubiquitin, has been examined by NMR and CD spectroscopy.

16 lained by thermal denaturation studies using CD spectroscopy.

17 This was verified by CD spectroscopy.

18 g urea-induced unfolding monitored by far-UV CD spectroscopy.

19 mutant (P34-hNPY) have been characterized by CD spectroscopy.

20 , with DNA have been investigated by NMR and CD spectroscopy.

21 a centrifugation assay, Tm measurements, and CD spectroscopy.

22 anganese Stabilizing Protein as monitored by CD spectroscopy.

23 similar secondary structures on the basis of CD spectroscopy.

24 hods, and their interactions were studied by CD spectroscopy.

25 typical cysteine-knot fold, as evidenced by CD spectroscopy.

26 el, which is undetectable using conventional CD spectroscopy.

27 ATR, human SMG-1, and human TRRAP by NMR and CD spectroscopy.

28 shed by single crystal X-ray diffraction and CD spectroscopy.

29 substitutions and analyzed by using NMR and CD spectroscopy.

30 ized, and helical content was assessed using CD spectroscopy.

31 g the information previously obtainable from CD spectroscopy.

32 olabile in the absence of NADPH as judged by CD spectroscopy.

33 mer, as determined using circular dichroism (CD) spectroscopy.

34 NA-bending assays and by circular dichroism (CD) spectroscopy.

35 ng calorimetry (DSC) and circular dichroism (CD) spectroscopy.

36 etic resonance (NMR) and circular dichroism (CD) spectroscopy.

37 (T(m)) measurements and circular dichroism (CD) spectroscopy.

38 h TnsD were monitored by circular dichroism (CD) spectroscopy.

39 f recombinant ERalpha by circular dichroism (CD) spectroscopy.

40 rements and using far-UV circular dichroism (CD) spectroscopy.

41 esicles, were studied by circular dichroism (CD) spectroscopy.

42 s divalent cations using circular dichroism (CD) spectroscopy.

43 ow-frequency S-band) and circular dichroism (CD) spectroscopy.

44 ce infrared (ATR-IR) and circular dichroism (CD) spectroscopy.

45 ored by fluorescence and circular dichroism (CD) spectroscopy.

46 an fluorescence (FL) and circular dichroism (CD) spectroscopy.

47 with P4, as confirmed by circular dichroism (CD) spectroscopy.

48 s aqueous solution using circular dichroism (CD) spectroscopy.

49 r magnetic resonance and circular dichroism (CD) spectroscopy.

50 variable-temperature variable-field magnetic CD spectroscopies.

51 apid-mixing stopped-flow, high-pressure, and CD spectroscopies.

52 were monitored by DSC and far-UV and near-UV CD spectroscopies.

53 form infrared (FT-IR) and circular dichroic (CD) spectroscopies.

54 Circular dichroism (CD) spectroscopy (263 nm) clearly detects two transition

55 Using CD spectroscopy, a competitive zinc binding assay, and a

56 Herein, we demonstrate that CD spectroscopy, a technique that is used primarily to e

57 the dG adducts was unequivocally assigned by CD spectroscopy after separation of each individual dias

58 zed conotoxin H-superfamily, we used NMR and CD spectroscopy along with MS-based analyses to investig

59 The receptors were characterized by CD spectroscopy, analytical ultracentrifugation, and bin

60 iochemically using X-ray crystallography, UV-CD spectroscopy, analytical ultracentrifugation, and ITC

61 By the use of light-scattering, CD spectroscopy, analytical ultracentrifugation, and try

62 UV-vis absorbance, CD spectroscopy, analytical ultracentrifugation, redox p

63 k, resonance Raman and UV-visible absorption/CD spectroscopies and MS were used to characterize the i

64 eries of tryptophan zippers by static IR and CD spectroscopies and the IR temperature jump method.

65 We applied CD spectroscopy and (125)I radioprobing to determine the

66 elix formed by the host, as shown by NMR and CD spectroscopy and a solid-state structure.

67 CD spectroscopy and amide HDX of the UBI-SDS(n) complexe

68 ies of each individual EF-hand peptide using CD spectroscopy and analytical ultracentrifugation.

69 ary structures were similar as determined by CD spectroscopy and both proteins bound at multiple site

70 s an i-motif structure in vitro, as shown by CD spectroscopy and chemical footprinting.

71 We combine these measurements with visible CD spectroscopy and cross-linking experiments to demonst

72 For the present paper, CD spectroscopy and DMS methylation techniques were used

73 lix (HTH) motifs was investigated by NMR and CD spectroscopy and found to retain the same overall sol

74 CD spectroscopy and guanidine hydrochloride denaturation

75 By using AFM, leakage assays, CD spectroscopy and in silico tools, we found that Pa-MA

76 CD spectroscopy and limited proteolysis experiments defi

77 The duplexes were investigated by CD spectroscopy and MD simulations.

78 crystallization from CHCl3/acetonitrile, and CD spectroscopy and optical rotation show that the resol

79 CD spectroscopy and second-derivative UV spectra indicat

80 ned using more established techniques (e.g., CD spectroscopy and SUPREX).

81 CD spectroscopy and the structure of an engineered disul

82 CD spectroscopy and thermal melts using Tpm3.1 peptides

83 Moreover, CD spectroscopy and thermally induced unfolding studies

84 equential arrangements and investigated with CD spectroscopy and UV melting curve analysis.

85 tic resonance (EPR), and circular dichroism (CD) spectroscopies and thermal denaturation studies.

86 of the novel hexamers by circular dichroism (CD) spectroscopy and (1)H-(13)C heteronuclear single qua

87 Circular dichroism (CD) spectroscopy and (1)H-(15)N heteronuclear single-qua

88 pc72 was demonstrated by circular dichroism (CD) spectroscopy and a fluorescence resonance energy tra

89 The method utilizes circular dichroism (CD) spectroscopy and a sensing ensemble composed of 2-fo

90 Circular dichroism (CD) spectroscopy and analytical ultracentrifugation indi

91 e protein as assessed by circular dichroism (CD) spectroscopy and biological activity.

92 ow synchrotron-radiation circular dichroism (CD) spectroscopy and describe the design of such a beaml

93 ructure and stability by circular dichroism (CD) spectroscopy and differential scanning calorimetry (

94 Circular dichroism (CD) spectroscopy and electron microscopy show that the Q

95 r KCl using two methods: circular dichroism (CD) spectroscopy and electrophoretic mobility shift assa

96 ructure was indicated by circular dichroism (CD) spectroscopy and enzymatic footprinting with RNase T

97 structure and function, circular dichroism (CD) spectroscopy and homology modeling were used to dete

98 mal melting experiments, circular dichroism (CD) spectroscopy and plasmid unwinding assays.

99 Circular dichroism (CD) spectroscopy and RNA thermal denaturation revealed a

100 physical methods such as circular dichroism (CD) spectroscopy and sedimentation velocity analytical u

101 es have been observed by circular dichroism (CD) spectroscopy and thermogravimetric analysis (TGA).

102 In the present report, circular dichroism (CD) spectroscopy and transmission electron microscopy (T

103 plexes were evaluated by circular dichroism (CD) spectroscopy and UV absorption melting studies of tr

104 mal aggregation assay, gel filtration study, CD spectroscopy, and bis-ANS interaction studies.

105 size-exclusion chromatography (SEC), far-UV CD spectroscopy, and catalytic activity measurements, an

106 Thermal denaturation, CD spectroscopy, and gel filtration experiments showed t

107 racentrifugation, fluorescence spectroscopy, CD spectroscopy, and guanidine-HCl denaturation were use

108 Site-directed mutagenesis, CD spectroscopy, and immunocytochemistry reveal that a p

109 nzymes as determined by fluorescence, far-UV CD spectroscopy, and incubation-induced rest activity sh

110 ated and characterized using metal analyses, CD spectroscopy, and kinetic studies.

111 repeat-containing regions by gel filtration, CD spectroscopy, and negative-staining electron microsco

112 nova have been probed by Raman spectroscopy, CD spectroscopy, and nondenaturing gel electrophoresis.

113 by using nanoESI- and IM-mass spectrometry, CD spectroscopy, and protein chemical modification react

114 icroscopy, attenuated total reflection-FTIR, CD spectroscopy, and SDS-PAGE.

115 nactive (AApep; G's replaced by A's) TMDs by CD spectroscopy, and then their effects on the kinetics

116 of DNAs and oligonucleotides was measured by CD spectroscopy, and this allowed determination of a DNA

117 sing steady-state fluorescence spectroscopy, CD spectroscopy, and time-correlated single-photon count

118 Thioflavin T (ThT) fluorescence, CD spectroscopy, and transmission EM analysis revealed t

119 ing EI by sedimentation velocity, by near UV CD spectroscopy, and with a nonphosphorylatable active s

120 ME/GC), fluorescence and circular dichroism (CD) spectroscopies, and docking studies.

121 matography (SEC), far-UV-circular dichroism (CD) spectroscopy, and catalytic activity measurements ov

122 RetGC1, characterized by circular dichroism (CD) spectroscopy, and investigated for protease resistan

123 on chromatography (SEC), circular dichroism (CD) spectroscopy, and stopped-flow kinetic analyses.

124 ature (Tm) measurements, circular dichroism (CD) spectroscopy, and the ethidium bromide (EB) displace

125 CD spectroscopy, appropriately designed peptide controls

126 The assets of CD spectroscopy are that the signal is directly linked t

127 Here, NMR and CD spectroscopy are used to characterize the role of imi

128 ation, fluorescence, and circular dichroism (CD) spectroscopy as a function of pH.

129 noncanonical helix were conducted by NMR and CD spectroscopy, as well as by X-ray crystallography and

130 e and cocoa were studied by fluorescence and CD spectroscopy at pH values of the gastrointestinal tra

131 l stability monitored by circular dichroism (CD) spectroscopy at 222 nm of 100 heterodimers that cont

132 ractions were studied by circular dichroism (CD) spectroscopy at pH 7 and 2.

133 ll cultures and a PD mouse model, along with CD spectroscopy, atomic force microscopy, immunofluoresc

134 be determined from spectra is a testament to CD spectroscopy being a very powerful technique.

135 lify how the advantages offered by automated CD spectroscopy can be exploited to quantify protein sta

136 CD spectroscopy confirmed the alpha-helical content of s

137 Circular dichroism (CD) spectroscopy confirmed that a substantial fraction o

138 Structural analysis by CD spectroscopy coupled with molecular dynamics simulati

139 the global thermodynamic analysis of DSC and CD spectroscopy data, which led to a detailed descriptio

140 CD spectroscopy demonstrated that the TMAO-induced struc

141 CD spectroscopy demonstrates that the conformation of rh

142 CD spectroscopy did not detect any optical activity in t

143 s, such as intrinsic fluorescence and far-UV CD spectroscopy did not show significant conformational

144 Data from CD spectroscopy, dynamic light scattering, analytical ul

145 At pH 7, CD spectroscopy, dynamic light scattering, and different

146 by kinetic and thermodynamic methods, using CD spectroscopy, dynamic light scattering, and scanning

147 Circular dichroism (CD) spectroscopy experiments indicated that bacterial me

148 opy, depth-dependent fluorescence quenching, CD-spectroscopy experiments, and MD simulations indicate

149 optical methods such as circular dichroism (CD) spectroscopy, fibrillogenesis is typically measured

150 ogeneity, and studied by circular dichroism (CD) spectroscopy, fluorescence spectroscopy, and initial

151 up2p structure by far-UV circular dichroism (CD) spectroscopy, Fourier transform infrared (FTIR) spec

152 estimation of protein secondary structure by CD spectroscopy from 29 to 37 proteins by including 3 ad

153 th transmission EM, atomic-force microscopy, CD spectroscopy, FTIR spectroscopy, analytical ultracent

154 Circular dichroism (CD) spectroscopy gave ellipticity minima and maxima at 2

155 ecyl phosphocholin (DPC) micelles by UV-vis, CD spectroscopy, gel electrophoresis, and analytical ult

156 Magnetic CD spectroscopy has been used due to its established abi

157 However, CD spectroscopy has remained a low-throughput method bec

158 CD spectroscopy has special relevance for the study of m

159 Circular dichroism (CD) spectroscopy has become established as a key method

160 f the I1 intermediate by circular dichroism (CD) spectroscopy has shown that I1 retains a significant

161 the thermal unfolding curve (as measured by CD spectroscopy) hint at a well ordered stable fold.

162 Sedimentation and CD spectroscopy identified that phosphorylation of Thr(1

163 s demonstrated by mass spectrometry, NMR and CD spectroscopy in combination with quantum chemical cal

164 CD spectroscopy in solution and a crystal structure of a

165 ) were characterized by multinuclear NMR and CD spectroscopy in solution and by X-ray crystallography

166 ndent conformational transitions detected by CD spectroscopy in the far UV indicate a more ordered st

167 ntitative agreement with circular dichroism (CD) spectroscopy in detecting the domain melting transit

168 FTIR and CD spectroscopy indicate all six peptides adopt a stable

169 In vitro kinetic studies monitored by CD spectroscopy indicate that [2Fe-2S] clusters on GrxS1

170 NMR and CD spectroscopy indicate this small fusion module compri

171 sults of fluorometry and circular dichroism (CD) spectroscopy indicate that the main phase of thermal

172 the secondary structures of the variants by CD spectroscopy indicated significant random-coil format

173 CD spectroscopy indicated that association with ATCase d

174 CD spectroscopy indicated that the peptide adopted a str

175 Far-UV CD spectroscopy indicated that the secondary structure o

176 Near-UV CD spectroscopy indicated that these impairments are cau

177 CD spectroscopy indicated that wild-type AQP2 and the ph

178 orescence quenching, and circular dichroism (CD) spectroscopy indicated that the high solubility was

179 er normal physiological conditions; however, CD spectroscopy indicates that in the presence of hydrox

180 CD spectroscopy indicates that N-218 MLN64 is largely al

181 CD spectroscopy indicates that rHb (alphaH87G) and rHb (

182 Circular dichroism (CD) spectroscopy indicates that Notch ankyrin polypeptid

183 Circular Dichroism (CD) spectroscopy is a long-established technique for stu

184 Circular Dichroism (CD) spectroscopy is a powerful method for investigating

185 Circular dichroism (CD) spectroscopy is a powerful method for monitoring con

186 Circular dichroism (CD) spectroscopy is a well-established technique for stu

187 Circular dichroism (CD) spectroscopy is a widely used method for examining t

188 Circular dichroism (CD) spectroscopy is extensively utilized for determining

189 Circular dichroism (CD) spectroscopy is one of the most useful techniques fo

190 Circular dichroism (CD) spectroscopy is widely used in structural biology as

191 a, designated PLDalpha C2 and PLDbeta C2, by CD spectroscopy, isothermal titration calorimetry, and p

192 Here, using CD spectroscopy, isothermal titration calorimetry, and s

193 ation dependence of alpha-helix formation in CD spectroscopy, it is likely that these oligomers assem

194 By CD spectroscopy, K16-OA-Abeta and K28-OA-Abeta had incre

195 tudies using analytical ultracentrifugation, CD spectroscopy, limited proteolysis, and (1)H NMR show

196 CD spectroscopy measuring the thermal unfolding of NKX3.

197 vation of low-melting ferritin subdomains by CD spectroscopy (melting midpoint 53 degrees C), account

198 UV-visible, EPR, and CD spectroscopies, metal analysis, and x-ray crystallogr

199 ssembly was confirmed by circular dichroism (CD) spectroscopy, microscopic images, and crystal struct

200 Circular dichroism (CD) spectroscopy monitored the thermal denaturation of 3

201 e complexes using steady-state fluorescence, CD spectroscopy, NMR, and native gel mobility shift assa

202 y structure content from circular dichroism (CD) spectroscopy, obtained using synchrotron light, show

203 Characterization by 1H NMR and CD spectroscopies of the resulting aptamers, TBA-T7b and

204 CD spectroscopy of a 37-mer model of alpha4 (residues 24

205 Far-UV CD spectroscopy of decorin and biglycan proteoglycans in

206 CD spectroscopy of DHFR and G121V-DHFR indicated that th

207 Conformational analysis using CD spectroscopy of purified, recombinant ECD2 protein de

208 Far-UV CD spectroscopy of StAR in PC membranes show more beta-s

209 he two 11-mer migration products followed by CD spectroscopy of the isolated adducted nucleosides ind

210 CD spectroscopy of the peptide in dodecyl phosphocholine

211 NMR and CD spectroscopy of the protein indicates that the glycan

212 CD spectroscopy of TMX-1 in oriented multilayers formed

213 s estimated using far-UV circular dichroism (CD) spectroscopy of all but Phe variants at position 30

214 tructure, as revealed by circular dichroism (CD) spectroscopy of recombinant proteins.

215 Circular dichroism (CD) spectroscopy of the apoE CT domain reveals spectra c

216 tron microscopy (EM) and circular dichroism (CD) spectroscopy of the nonmotor region shows characteri

217 gh each 32-mer formed stable triple helices (CD) spectroscopy, only 1a and 1b self-assembled into mic

218 c bases for these observations, here we used CD spectroscopy, photo-induced cross-linking of unmodifi

219 d physiological urea (1 mm) and monitored by CD spectroscopy, protein crystallography, and Fe2+ relea

220 Circular dichroism (CD) spectroscopy proves that these peptides are highly a

221 Circular dichroism (CD) spectroscopy provides rapid determinations of protei

222 asurements of the D-Arg peptide monitored by CD spectroscopy reveal an apparent two-state helix-coil

223 UV-vis and CD spectroscopy reveal that a stable hybrid possessing G

224 UV-vis and CD spectroscopy reveal that the quadruplex structure of

225 In addition, protein fingerprinting and CD spectroscopy reveal the flexibility of 3betaHSD2, a n

226 CD spectroscopy revealed a series of sequential conforma

227 CD spectroscopy revealed that a conformational change oc

228 However, CD spectroscopy revealed that the addition of certain tr

229 EPR and CD spectroscopy revealed that the membrane restrains rho

230 CD spectroscopy revealed that the mutant receptors have

231 Biophysical studies using NMR and CD spectroscopy revealed that UBXD1-N can be classified

232 lymerase stop assay, and circular dichroism (CD) spectroscopy revealed that the G-quadruplex containi

233 ral analysis of duplexes with DNA and RNA by CD-spectroscopy revealed a shift from B- to A-type confo

234 CD spectroscopy reveals that, in the presence of the sma

235 CD spectroscopy showed that the 33-mer peptide P3W folds

236 in the presence of vesicles, and difference CD spectroscopy showed that the transmembrane regions of

237 modifications were identified using MS, and CD spectroscopy showed the receptor to be approximately

238 Circular dichroism (CD) spectroscopy showed that the detergent-solubilized p

239 ions, monitored by UV-visible absorption and CD spectroscopy, showed that a [4Fe-4S](2+) cluster-boun

240 Surprisingly, CD spectroscopy shows a stable parallel G-quadruplex str

241 enatured ferrous protein, fast time-resolved CD spectroscopy shows a submillisecond folding process t

242 i, and i + 1, i + 2, or i + 3 arrangements, CD spectroscopy shows that As(III) coordination causes h

243 CD spectroscopy shows that it is approximately 45% alpha

244 CD spectroscopy shows that the structure is unimolecular

245 CD spectroscopy shows that these structures' helical sen

246 idinium unfolding of myoglobin, monitored by CD spectroscopy, shows destabilization at less than 1.3

247 that was high in alpha-helix as measured by CD spectroscopy, similar to the normal cellular isoform

248 ared and characterized using metal analyses, CD spectroscopy, steady-state kinetics, stopped-flow flu

249 h Raman spectroscopy and circular dichroism (CD) spectroscopy structural analysis we were able to sep

250 NMR and CD spectroscopy studies demonstrated that [F9A]AuIB reta

251 Structural analysis of Atm1-C by CD spectroscopy suggested a similarity of secondary stru

252 CD spectroscopy suggests that Rv2302 partially unfolds u

253 se previously undescribed photosensors using CD spectroscopy supports a structurally heterogeneous ch

254 the C 499D mutant protein by absorbance and CD spectroscopy supports the conclusion that its bilin c

255 etic resonance (NMR) and circular dichroism (CD) spectroscopy supports the hypothesis that increasing

256 Circular dichroic (CD) spectroscopy supports this folding and self-assembly

257 Here, we show by NMR and CD spectroscopy that LcrG lacks a tertiary structure and

258 Here we show using NMR and CD spectroscopy that the C9orf72 hexanucleotide expansio

259 luding heterocomplex pulldown assays, far-UV CD spectroscopy, the thioflavin T binding assay, transmi

260 Using circular dichroism (CD) spectroscopy, the thermal stability of these protein

261 action with the G4DNA has been obtained from CD spectroscopy, thermal denaturation, and UV-vis titrat

262 tertiary structure as determined by near UV CD spectroscopy, thermal denaturation, sedimentation equ

263 , and then studied by using a combination of CD spectroscopy, Thioflavin T fluorescence, EM, atomic f

264 sidue 133) long overhand loops were found by CD spectroscopy to have helical contents similar to that

265 ) were purified to homogeneity and judged by CD spectroscopy to have structures similar to that of th

266 nalysis of AlkB using NMR, fluorescence, and CD spectroscopy to show that AlkB is a dynamic protein e

267 infrared (ATR-FTIR) and circular dichroism (CD) spectroscopies to identify secondary and dynamic str

268 on calorimetry (ITC) and circular dichroism (CD) spectroscopy to characterize the binding of soluble

269 ve used fluorescence and circular dichroism (CD) spectroscopy to characterize the effects of calcium

270 ry dispersion (ORD), and circular dichroism (CD) spectroscopy together with density functional theory

271 blish the versatility of circular dichorism (CD) spectroscopy toward understanding aggregation of mon

272 Circular dichroism (CD) spectroscopy, Triton X-114 (TX-114) phase partitioni

273 Based on results of CD spectroscopy, trypsin treatment, and MS, we propose a

274 changes in the DNA molecule were detected by CD spectroscopy upon protein-DNA complex formation.

275 In contrast to CD spectroscopy, UV absorbance spectroscopy shows only a

276 wed its characterization by EPR, UV-vis, and CD spectroscopies, validating spin-delocalization throug

277 ariable-temperature, variable-field magnetic CD spectroscopies was applied to HmaS and compared with

278 Moreover, CD spectroscopy was applied to the mutant NP7(E27Q) and

279 Far-UV CD spectroscopy was employed for detection of conformati

280 A combination of HPLC, optical rotation and CD spectroscopy was employed to distinguish stereoisomer

281 Steady-state CD spectroscopy was utilized to characterize the peptide

282 Circular dichroism (CD) spectroscopy was employed to show that the alcohol s

283 Circular dichroism (CD) spectroscopy was used to monitor the urea-induced un

284 Using CD spectroscopy, we find that approximately 1 mol eq of

285 Using UV-visible and CD spectroscopy, we found that P450 21A2 thermal stabili

286 n using Thioflavin T fluorescence and far-UV CD spectroscopy, we have found that the aggregation of A

287 Using CD spectroscopy, we provide evidence that hSloRCK2 under

288 ration calorimetry, and thermal denaturation CD spectroscopy, we show that both subdomains are requir

289 revious study using peptide design, EPR, and CD spectroscopy, we showed that the HGGGW segment within

290 Using circular dichroism (CD) spectroscopy, we demonstrate that urea promotes form

291 By employing circular dichroism (CD) spectroscopy, we demonstrated that the lipopeptides,

292 Using on-surface circular dichroism (CD) spectroscopy, we have investigated the structure of

293 tweezers instrument and circular dichroism (CD) spectroscopy, we provide compelling evidence that hi

294 both 1H NMR and visible-circular dichroism (CD) spectroscopy, we show that two Ni2+ ions bind to His

295 Folding experiments of T1-892 using CD spectroscopy were carried out at varying concentratio

296 with Trp fluorescence and near-UV and far-UV CD spectroscopy were performed on variants with Lys-66,

297 ogues, conformation-specific antibodies, and CD spectroscopy were used to evaluate the basis of the e

298 n lipid membrane environments, using NMR and CD spectroscopy with lipid micelle and lipid bilayer sam

299 was further indicated in circular dichroism (CD) spectroscopy with a positive (A) or negative (B) Del

300 red (FTIR) spectroscopy, circular dichroism (CD) spectroscopy, X-ray diffraction (XRD), and solid-sta