ライフサイエンスコーパス: complex ion

1 res corresponding to hemoglobin subunit-heme complex ions.

2 lculations on all of the observed Co(I) dppe complex ions.

3 um dications by forming [FA - H + MgPhen](+) complex ions.

4 - complex ions compared with the Fe(II)-/Mg- complex ions and divalent metal carbonates.

5 Here, protein and protein complex ions are formed directly from a 150 mM KCl and 2

6 The respective mono- and dibenzene complex ions are isolated in an ion-trap mass spectromet

7 native-like protein, and native-like protein complex ions are reported here, forming a database of co

8 cine), and [Mn(II) + (l-Phe-Gly - H) + M](+) complex ions are used to determine collision cross secti

9 source temperature on native protein-ligand complex ions as assessed by SID.

10 omprehensive unfolding of large multiprotein complex ions as well as interplatform CIU comparisons.

11 ectroelectrochemical characterization of the complex ion at an ITO optically transparent electrode to

12 lective electrostatic adsorption of non-zinc complex ions at alkaline conditions.

13 he direct formation of intact protein-ligand complex ions by spraying ligands toward separate protein

14 he permeation and gating regions within this complex ion channel have implications in identifying sma

15 hypotheses for further investigation of this complex ion channel.

16 RF3 critical for its formation of multimeric complexes, ion channel activity, and, ultimately, releas

17 sults are general and can be applied to more complex ion channels, providing insight into ion channel

18 s for probing the functional architecture of complex ion channels.

19 Examples include receptor tyrosine complexes, ion channels, transporters, and G protein-cou

20 igand must have higher stability for Ni-/Co- complex ions compared with the Fe(II)-/Mg- complex ions

21 Collision activation of this complex ion delivered evidence for the gas-phase reactio

22 mitters are used to form protein and protein complex ions directly from high-ionic-strength (>150 mm)

23 ption is particularly challenging due to the complex ion dynamics, disordered structures, and hierarc

24 Protein complex ions (e.g., superoxide dismutase, enolase, and h

25 This study provides insight into complex ion effects on protein stability and serves as a

26 eparation of native-like protein and protein complex ions expands the structural information availabl

27 dings not only help the understanding of the complex ion flow patterns at Venus but also suggest that

28 ; rather, these batteries rely on monovalent complex ions for their main redox reaction.

29 ive mass spectrometry of protein and protein complex ions formed from a buffer containing physiologic

30 icated reaction is catalyzed by paramagnetic complex ions giving rate constants that are proportional

31 h supercharging reagents resulted in protein complex ions having increased multiple charging without

32 ate the reduction of Sn(IV) as the hexabromo complex ion in a 2 M HBr-4 M NaBr medium.

33 take, retention, and optical response of the complex ion in the Nafion film.

34 ridyl)-s-triazine, which forms a blue-violet complex ion in the presence of ferrous ions.

35 e the extent of salt adduction to ligand-DNA complex ions, including in the presence of relatively hi

36 ceratodes blood cells, intrinsic aquo-VSO4+ complex ion is indicated by an inflection feature at 547

37 roscopic data indicate that, in the tungsten complex ion IV(+), the single electron is delocalized ov

38 f dipicolinic acid, amino acids, and calcium complex ions made in the spore mass spectra.

39 s capable of much higher resolution and more complex ion manipulations.

40 ing trace analyte ions that are present in a complex ion mixture to a mass spectrometer (MS) for iden

41 s served to extract bacterial peaks from the complex ion mobility spectra of intact microorganisms an

42 ed ESI-MS spectra showing only protein-dsDNA complex ions of 1:1 stoichiometry and free dsDNA.

43 simulations, indicating that the effects of complex ions on proteins are increasingly predictable in

44 come more negatively charged, the "successor-complex" ion pairs are subject to larger anion-anion rep

45 H) coupling constants revealed for DSI/imine complexes ion pairs with very weak hydrogen bonds.

46 section (CCS) values for protein and protein complex ions ranging from 6-1600 kDa, exhibiting an aver

47 to separate native-like protein and protein complex ions ranging in mass from 12 to 145 kDa.

48 CD indicates a complex ion-specific destabilization of the alpha-helix

49 Fragile transition metal complex ions such as [Cr(H2O)4Cl2](+), difficult to be o

50 To illustrate the application to mixtures of complex ions, the 10+ charge state of bovine ubiquitin w

51 trometry by adducting to protein and protein complex ions, thereby reducing sensitivity and mass meas

52 The trimeric complex ion (three chiral ligands-2 mol of the analyte a

53 The trimeric complex ions (three chiral ligands--one of the analyte a

54 hing iso-cross-sectional protein and protein complex ions through their distinct unfolding pathways i

55 The resulting complex ion, tris(2,2'-bipyridyl)iron(II), Fe(bipy)3(2+)

56 correct molar extinction coefficient of this complex ion under FRAP assay conditions has never been p

57 to carry away excess energy from the protein complex ion upon activation and can result in significan

58 by soft and reactive landing (SL and RL) of complex ions was implemented on a mass-selected ion depo

59 result suggests that for protein and protein complex ions within this mass range, there is no inheren