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1 -center containing proteins (homo and hetero metal ions).
2 on, and the nature of the centrally chelated metal ion.
3 of the aqueous medium, and the nature of the metal ion.
4 reaction has been exploited for sensing of a metal ion.
5  not significantly affected by the choice of metal ion.
6 nvolved in the coordination of the substrate metal ion.
7 nd most selective binding towards a specific metal ion.
8 le that of the pistol ribozyme is a hydrated metal ion.
9 e radical complexes without oxidation of the metal ion.
10 e, and each vertex is occupied by a divalent metal ion.
11 ld(I/III) ions but is nonemissive with other metal ions.
12 umns for the enhanced extraction of multiple metal ions.
13 ation effects in the absence of paramagnetic metal ions.
14 atalyzed by naturally occurring minerals and metal ions.
15 mer that binds several biologically relevant metal ions.
16 ive, 'one-pot' coordination of soft and hard metal ions.
17 class of ratiometric fluorescent sensors for metal ions.
18 ctural stabilization of this domain by bound metal ions.
19 forming the coordination assemblies with the metal ions.
20 ng affinity toward a broad range of divalent metal ions.
21 ins that interact with endogenous lipids and metal ions.
22 cess through addition of differently charged metal ions.
23 le reduction and oxidation of the transition metal ions.
24 5 allows an adequate catalytic effect of the metal ions.
25 large oligomeric states with the addition of metal ions.
26 rase active site without involving catalytic metal ions.
27 bled with Mn, Fe, Co, Ni, Cu, or Zn bridging metal ions.
28 e the redox centers to reversibly react with metal ions.
29  to relatively high concentrations of Ca(2+) metal ions.
30  9%, and afterwards by its complexation with metal ions.
31 ical conductivity is provided by sorption of metal ions.
32  based on CsPbX(3) NCs doped with transition metal ions.
33 n by eliminating the release of heavy metals/metal ions.
34 antiopure tetrahedral cages of square-planar metal ions.
35 ite that positions the 5'SS at two catalytic metal ions.
36 c DNA, AA-TT condenses in all alkaline earth metal ions.
37  cage held together exclusively by trivalent metal ions.
38 ll as sensory materials for the detection of metal ions.
39 lves around its interactions with transition metal ions.
40 for the coordination of different transition metal ions.
41 IV) (O) intermediates binding redox-inactive metal ions (1-M(n+) ).
42 es as an ion pump that continuously provides metal ion activators that greatly promote the enzymatic
43 al ion intermittently bound close to the two-metal-ion active site, to which recessed ends or 5'-flap
44 nstruction, we were able to resolve a Zn(2+) metal ion adjacent to the coreceptor binding site, which
45 ntal insight into the thermodynamics driving metal-ion adsorption reactions and provides the specific
46 ched for phosphopeptides through immobilized metal ion affinity chromatography (IMAC), followed by en
47 g amount of gallium ion provides immobilized metal ion affinity for phosphopeptides enrichment.
48                                  Immobilized metal-ion affinity chromatography (IMAC) used to purify
49                                            A metal ion also plays an important role in ligand binding
50 ed to the requirement for both an open-shell metal ion and a redox non-innocent ligand.
51 ls and the resulting interaction between the metal ion and ligand.
52 ifier, functional class, bioinorganic class, metal ion and metal-containing cofactor, which will serv
53 recognizing As(III) in the presence of other metal ions and a complex matrix of waste water samples w
54 D, which are linked to different active site metal ions and coordination modes.
55  cooperative binding of a full complement of metal ions and deeper membrane insertion.
56 nto 3D lattices upon coordination of various metal ions and ditopic, hydroxamate-based linkers.
57 erentially modulated by oxidative stress and metal ions and induce distinct patterns of global gene e
58 versatile coordination chemistry of abundant metal ions and inexpensive organic ligands.
59                           The arrangement of metal ions and ligands in this pentametallic assembly wa
60 orks (MOFs) are hybrid materials composed of metal ions and organic linkers featuring high porosity,
61 nvolving frameworks based on a wide range of metal ions and organic linkers.
62 thalpy change showed that that adsorption of metal ions and other parameters was feasible, spontaneou
63  antiferromagnetically coupled chromium(III) metal ions and provides a classic example of a magnetic
64 rdination networks that incorporate chromium metal ions and pyrazine building blocks.
65  signaling and stress pathways, particularly metal ions and small molecules.
66 tudies revealed that PfA-M17 and Pv-M17 bind metal ions and substrates in a conserved fashion, althou
67 ups of proteins, the connectivity of the two metal ions and the chemistry each cofactor performs are
68  effective method to affect the reduction of metal ions and the formation of nanocrystals.
69                           The acquisition of metal ions and the proper maturation of holo-metalloprot
70 alkali, alkaline earth, transition and other metal ions and their global structural effects on alpha-
71   This enzyme was highly stable to different metal ions and was able to hydrolyze kappa-casein simila
72 tentially pre-organizing them for additional metal-ion and membrane-binding events.
73 s with nucleic acids, lipids, carbohydrates, metal ions, and aromatic molecules are discussed in rela
74 e ligands, pai-interactions, coordination to metal ions, and few halogen bonds in chloropyrazines.
75 inst pH changes and the presence of divalent metal ions, and their high homogeneity make them an effi
76 m ions given that complexes containing these metal ions are already in clinical use or have advanced
77                   Elevated levels of certain metal ions are found in protein aggregates in neurons of
78                                    Here, the metal ions are initially anchored onto the active bipyri
79                                              Metal ions are known to play various roles in living org
80                          More notably, heavy metal ions are removed effectively by forming hydrogen a
81 cation for heavy metal ion removal, as heavy metal ions are the most harmful and widespread contamina
82 lar switches, in conjunction with transition metal ions, are shown to operate as reversible polymer c
83 t are activated by the binding of transition metal ions as a promising class of antibiotics, and for
84 site bound beta-galactosidase on addition of metal ions as compared to the native and other bound enz
85 result of the synergistic effect of the five metal ions as Lewis acid in epoxide activation.
86 frameworks that contain at least 2 different metal ions as nodes of their frameworks.
87 ortionation of Jahn-Teller-active transition-metal ions, as exemplified by the broad classes of respe
88 ionally, our simulations show that the third metal ion assists the departure, through the mobile arch
89 ther hand, has endonuclease activity and one metal ion at the active site and is predominantly a mono
90 nfluence of temperature on the adsorption of metal ions at the solid-water interface is often overloo
91 lly abundant polyphenols (>8000 species) and metal ions available, the present cubosome-enabled strat
92 efficient mean to enhance the performance of metal-ion batteries by minimizing electronic and ionic t
93 e as ideal anodes for 'Rocking-Chair' alkali metal-ion batteries.
94 ly differing ligand preferences of competing metal ions become amplified by the coupling of local wit
95 hiometric concentrations of the investigated metal ions bind specifically to the N-terminal region of
96  electrostatic and chemical contributions to metal ion binding by nanoparticulate complexants, and th
97                             In all cases the metal ion binding dominated the velocity of the carrier.
98             Mutation of residues involved in metal ion binding impaired catalytic activity and the fo
99 herein the extent of band bending induced by metal ion binding is the primary driver of photoelectroc
100 for engineering such a selective multivalent metal ion binding site into target macromolecules for st
101 ng a clamshell and the structure defines two metal ion binding sites, one in each domain.
102                      The successive folding, metal ion binding, and disulphide acquisition steps in t
103 se results establish the structural basis of metal ion binding, transport and inhibition in ferroport
104 , or triazolo-pyridines, which should enable metal ion binding.
105   Metallothioneins, a group of cysteine-rich metal-ion binding proteins, are known to be a key physio
106 ive was to understand the role of individual metal-ion binding sites of these domains in the membrane
107 e propose a model that links the microscopic metal-ion binding to Abeta monomers to its macroscopic i
108 ences of delaying Abeta aggregation via weak metal-ion binding, quantitatively linking the contributi
109 rotein the conformational changes induced by metal-ion binding.
110  the silver ion, that, similarly to divalent metal ions, binds to monomeric Abeta peptide and efficie
111                                          The metal-ion bound state appears to be incapable of aggrega
112 eneration and properties of copper (or other metal ion) bound O(2)-derived reduced species, such as p
113 edox and thermodynamic relationships between metal-ion-bound O(2) and its reduced (and protonated) de
114  in many food products, through chelation of metal ions, breakdown of radical chains and hydrogen per
115 ility of His to coordinate Zn(2+) to promote metal ion bridges, and we have found that the histidine
116 embly of isostructural frameworks with mixed-metal ion bridges, or with clusters that have been doped
117              In experimental studies, we use metal-ion bridges to show that promoting an M101-F99 bon
118 e suggests that several enzymes use a single-metal ion, but the precise catalytic mechanism is unknow
119 lay key biological roles for a wide range of metal ions, but unlike many other metalloproteins, the s
120                  A cytosolic accumulation of metal ions can lead to mismetallation of proteins and ce
121  conventional intercalation cathodes, alkali metal ions can move in and out of a layered material wit
122 ncy of the immobilized enzyme in presence of metal ions can promote its economic use for lactose hydr
123 f the second magnesium necessary for the two-metal ion catalysis.
124  useful as ligands or gel matrixes for other metal-ion catalyzed organic reactions.
125  the administered compounds and that, if the metal ion changes its oxidation state in the cytosol as
126 model for flexible co-targeting, addition of metal ion chelators as models for imaging and radiothera
127 y can be ascribed to the presence of reduced metal ions, chemically or photochemically generated duri
128 y of six dimers controlled by their divalent metal ion cofactors.
129 res driven by coordination interactions with metal ions commonly present in environment and serve a s
130 al surfaces can be used to probe kinetics of metal ion complexation and establish the success of elec
131 ction and the genetic response to changes in metal ion concentrations.
132 organic ligands and square-planar transition metal ions connected into two-dimensional (2D) sheets st
133 ected metal oxides via the use of an aqueous metal-ion-containing photoresin is presented.
134 nd class offers interesting possibilities of metal ion coordination and hydrogen bond formation via i
135  not only provide deeper insight into PrP(C) metal ion coordination but they also suggest new perspec
136  IIs, we demonstrate that the characteristic metal ion coordination geometries (tetrahedral for Zn(2+
137 orter in direct contact with residues of the metal ion coordination site, thereby interfering with su
138 ds within a discrete layer by anion-template metal-ion coordination opens the way for the synthesis o
139                 In an unanticipated finding, metal-ion coordination was also found to translocate an
140 ding to a formal 2-electron reduction of the metal-ion core of FeMo-co.
141 ng stoichiometries found upon titration with metal ions correlate with their specific binding affinit
142                Here, we investigated whether metal ions could affect allele-dependent structural vari
143                  Exchanging Ni(II) for other metal ions could broaden the scope of metalloenzyme targ
144 (2+), Zn(2+), and Cd(2+), but not monovalent metal ions, Cr(3+), Mg(2+), Y(3+), Sr(2+) or Ba(2+).
145 gels to verify that stoichiometric excessive metal ion cross-linker concentrations can still result i
146 urthermore, we found that the binding of the metal ion Cu(2+) or Ni(2+), but not Mn(2+), Zn(2+), or H
147 ar photoactive complexes with Earth-abundant metal ions (Cu, Zr, Fe, Cr) for potential eco-friendly a
148 rand factor A domain containing a functional metal ion-dependent adhesion site (MIDAS) and an associa
149  will contribute to the development of novel metal ion-dependent protease inhibitors, which might hel
150 ins provide evidence that the proteins share metal ion-dependent RNA 3' polyadenylation activities th
151  toxin component is distinguished by a broad metal-ion-dependent endonuclease activity with specifici
152 luorescent proteins (FPs) have been used for metal ion detection.
153 lication to an important analytical problem, metal ion discrimination and quantitation, by constructi
154 ween the metalloproteins and the dye with no metal ion dissociation.
155 , the higher tendency of unwanted transition-metal-ion dissolution and side-reactions in Jahn-Teller-
156 isproportionation, phase transformation, and metal-ion dissolution in transition-metal oxides upon ex
157 (6) quaternary oxide with high uniformity of metal ion distribution as confirmed by electron microsco
158 resented show that MAS-DNP from paramagnetic metal ion dopants provides an efficient approach for pro
159 ughs in substituting precious and rare-Earth metal ions (e.g. Ru, Ir, Pt, Au, Eu) in these applicatio
160                                              Metal ions, especially Mg(2+), neutralize these negative
161 In this study, we found that the active site metal ions essential for catalytic activity have a secon
162     Moreover, transition and post-transition metal ions, establishing coordinative interactions with
163  can likely be applied to imaging many other metal ions, expanding the range of the current genetical
164  the important role that adsorption plays in metal-ion fate and transport in the natural environment
165 of a sea urchin HCN channel using transition metal ion fluorescence resonance energy transfer (tmFRET
166 t that S. aureus gyrase uses a single moving-metal ion for cleavage and that the central four base pa
167 natural metallonucleases relying on a single metal ion for their activity.
168                                    Pt and RE metal ions from the most common hydrated metal salts are
169 ry, for efficient remediation of trace heavy metal ions from water.
170              In addition, we reveal that the metal ions have a long-range (~10 angstrom) electrostati
171  only Al(3+) with no interference from other metal ions, having a limit detection of 0.5 and 2.1 uM,
172 uctural frameworks containing redox-inactive metal ions, highlighting the importance of energy alignm
173                               Disruptions in metal ion homeostasis have been described in association
174                                     However, metal ion homeostasis is a double-edged sword.
175  of group ECF56, regulates morphogenesis and metal-ions homeostasis during development to ensure the
176 ids, known for their gas storage ability(1), metal-ion immobilization(2), proton conduction(3), and s
177                           In C2A, a divalent metal ion in site 1 is sufficient to drive its weak asso
178                  The determination of nickel metal ion in the crab tissue, oyster tissue and rice sam
179  present study was the measurement of nickel metal ion in the real samples of crab, oyster and rice b
180  designed method for determination of nickel metal ion in the real samples.
181    Here, we report on the catalytic roles of metal ions in a model metalloenzyme system, human carbon
182 hly oxidizing radicals and bind redox-active metal ions in a similar manner as antioxidants used as m
183 s for ultrasensitive SERS-based detection of metal ions in complex fluids.
184 troscopy (ICP/OES) to trace some toxic heavy metal ions in eight select farmed and four select import
185 visualization of neuromelanin and associated metal ions in human brain tissue can be achieved using s
186         Our study provides evidence that the metal ions in metalloenzymes have a crucial impact on th
187                             Mixing different metal ions in one polymer offers another degree of contr
188                       The detection of these metal ions in several reference materials (CASS-4, SLEW-
189             Luminescence from Earth-abundant metal ions in solution at room temperature is a very cha
190  is proportional to the concentration of the metal ions in solution.
191          The mechanism for the adsorption of metal ions in tannery wastewater onto the nano-adsorbent
192             In addition to the two canonical metal ions in the active site, a third Mn(2+) that coord
193 , we investigate the effects of changing the metal ions in the M-HAB system, with HAB = hexaaminobenz
194 apability(6,7) owing to the high mobility of metal ions in the Si switching medium(8).
195 These results enlighten the roles of the two metal ions in the specificity of DNA polymerases.
196 dies reveal an intact active site with bound metal ions in the structure of YejM periplasmic domain.
197 the local ordering of lithium and transition metal ions in the transition metal layers.
198 iving organisms; therefore, the detection of metal ions in water resources is essential for monitorin
199                             We find that the metal-ion-induced folding can proceed with stereoinducti
200                     Here we study effects of metal ion interaction with alpha-synuclein at the molecu
201          These hExo1 structures show a third metal ion intermittently bound close to the two-metal-io
202 he difficulty in transforming the binding of metal ions into a change of fluorescent signal.
203                   Displacement of transition metal ions into the alkali metal layers has been propose
204 study also identifies the previously unknown metal ion involved in YbeY function to be Zn2+ and shows
205 on is highly elevated in AD brains, and this metal ion is believed to be an important player in the p
206  system containing exchangeable sites at the metal ion is re-cast as a surrogate of a coordinatively-
207                                              Metal ion leaching from the beads under storage and appl
208     Herein we quantitatively investigate how metal ion Lewis acidity and steric properties influence
209  and oxidative stress, both of which involve metal ions like copper, manganese and iron.
210  their replacement by complexes of essential metal ions, like Mn(II).
211 n staining is ideal for His-tag detection by metal ion-loaded and fluorescently labeled chelator head
212 imple approach, called UVHis-PAGE, that uses metal ion-loaded and fluorescently labeled chelator head
213 The His-tag can also be directly detected by metal ion-loaded nickel-nitrilotriacetic acid-based chel
214  complexation with seven divalent transition metal ions M(II) (M = Mn, Co, Ni, Cu, Zn, Pd, and Cd) un
215 emonstrating a remarkable IMAC-metalloenzyme metal ion match.
216 lecular dynamics simulations support the two-metal ion mechanism and the kinetic data indicating weak
217 he fidelity of DNA polymerases through a two-metal ion mechanism.
218 orted so far for catalysts based on a single metal ion mechanism.
219 nt luminescence nanoparticles (D-PLNPs) with metal ions (MIs) and for the first time proposed an MIs-
220 ly bind a wide array of first-row transition metal ions (Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(I
221  was demonstrated against 13 other competing metal ions (Na(+), K(+), Mg(2+), Ca(2+), Mn(2+), Fe(2+),
222  bridging N(2) ligand by employing different metal ions of differing Lewis acidities.
223 d to be independent of alkali salts or other metal ions, offering robustness with regard to samples c
224 es (OCS) when vacant Lewis acid sites on the metal ions or cluster nodes have been generated.
225 ous materials that can be readily built from metal ions or clusters and organic linkers.
226 dination bonding between organic ligands and metal ions or clusters.
227 al oxides for OER is still limited to either metal ions or lattice oxygen.
228 predict whether they can bind nucleic acids, metal-ions or are involved in chaperone functions.
229 ations are restricted to a limited number of metal ions owing to the lack of available metal-binding
230 eviously overlooked active sites, transition-metal-ion oxidation states, reaction intermediates, and
231      Importantly, cellular interactions with metal ions, particularly Ca(2+), have recently been repo
232 iments revealed that binding of one divalent metal ion per C2 domain results in loss of conformationa
233 rast agents as biosensors (in the sensing of metal ions, pH, enzymes, temperature, hypoxia, reactive
234 hat HIV reverse transcriptase binds only two metal ions prior to incorporation of a correct base pair
235  polymeric ligand coordinated with different metal ions produces elastomers with vastly different cha
236                          We observe that the metal ion profoundly influences the electrical conductiv
237 s, and additionally facilitates a regulatory metal ion-promoted interaction between the PrP(C) N- and
238 oring charge on the oxide and the transition metal ions, rather than on the transition metal alone(1-
239           This is the first example of using metal ion redox for the MR imaging of pathologic change
240 )](+).(H(2)O) (n) clusters indicate that the metal ion remains directly bound to the head group in a
241 discuss their field of application for heavy metal ion removal, as heavy metal ions are the most harm
242 tle direct spectroscopic confirmation of the metal ion's coordination details.
243 dent on the occupancy and orientation of the metal ion's d-orbitals and the resulting interaction bet
244 ther, our results indicate that upon partial metal ion saturation of the intra-loop region, Syt1 adop
245                        The interplay between metal ion sensing and metal-dependent expression of viru
246 ons of residues anchoring this non-catalytic metal ion severely impair DNA binding and cleavage.
247 the tighter 5(2) knot can bind two different metal ions simultaneously, the looser 3(1) isomer can bi
248 tion correlates with the occupancy of the C2 metal ion sites.
249  ions is verified by screening six different metal ion solutions containing potentially interfering i
250 s multiway junctions or pseudoknots in mixed metal ion solutions.
251  delineated for determining intraparticulate metal ion speciation, and for evaluating intrinsic chemi
252 the protein states with well-defined protein-metal ion stoichiometry.
253 n(II) with respect to trans-chelation with a metal ion such as Cu(II).
254 or H(+), Na(+), K(+), Ca(2+), and transition metal ions such as Cu(I), Zn(II), and Cd(II).
255 good selectivity toward Hg(2+) against other metal ions such as V(4+), Pb(2+), Cr(3+), Cd(2+), Cu(2+)
256 aches to limit the availability of key heavy metal ions such as zinc and iron.
257                   The effect of other alkali metal ions (such as Li and K) on the enantioselectivity
258                                   Transition metal ions, such as water-soluble iron (WS-Fe), are toxi
259 re we demonstrate that by using an anion and metal ion template, woven molecular 'tiles' can be tesse
260 ing effect for any other divalent transition metal ions tested, including Mn(2+), Fe(2+), Co(2+), Ni(
261 riations in the numbers and positions of the metal ions that perverted the active sites into off-path
262 esence of heterogeneous spatial sequences of metal ions that we describe, depending on the metal and
263 e or decompose in the presence of transition metal ions, the reactivity of this metastable species is
264 ensity redistribution from Fe-H bonds to the metal ions themselves enables N(2) to bind with concomit
265  M/COF-DB allows for the easy replacement of metal ions through a postsynthetic exchange.
266  conformational flipping of Glu89 allows one metal ion to be recruited from the bulk and promptly pos
267  order for a scissile phosphate to attract a metal ion to the A-site to catalyze cleavage, after whic
268        Manipulating symmetry environments of metal ions to control functional properties is a fundame
269 tures can serve as ligands and assemble with metal ions to form MOFs.
270                                   Binding of metal ions to library compounds and substrates is an und
271 secondary site, which both serves to attract metal ions to the ferroxidase center and acts as a flow-
272 ng of cellular levels of ligand and divalent metal ions to tightly control gene expression.
273 mulation using customized enzyme activators (metal ions) to directly construct metal-organic framewor
274  top of all these advantages, intermolecular metal-ion translocation is a well-known factor in biolog
275    CorA, a divalent-selective channel in the metal ion transport superfamily, is the major Mg(2+)-inf
276 se findings reveal that MavN is a transition-metal-ion transporter that plays a critical role in resp
277          In wild type plants, genes encoding metal ion transporters, such as copper, iron and zinc tr
278 trategies to maintain access to bioavailable metal ions under conditions of extreme restriction of tr
279 opyran-functionalized polymer and transition metal ions underwent reversible thermally triggered (lig
280                            We determine that metal ion uptake does not act as a rigidification elemen
281                                              Metal ions, usually bound by various amino-acid side cha
282 welve uncoordinated pyridyl units around its metal-ion vertices.
283 array of monovalent, divalent, and trivalent metal ions, we demonstrated that this metal binding site
284 ince serine proteases are often sensitive to metal ions, we investigated the influence of different d
285 030-5.0 ug L(-1) for determination of nickel metal ion were obtained.
286 ce-the extraction efficiencies of the listed metal ions were all greater than 99.2%, and the detectio
287                 The following representative metal ions were examined: Pb, Cd, Zn, Ce (III), Ba, Ni,
288 f fluorescence response to Fe(3+) over other metal ions which was attributed to a charge transfer mec
289 able to form coordination bonds with various metal ions, which can be reduced to metal nanoparticles
290 gand field splitting of first-row transition metal ions, which leads to efficient nonradiative deacti
291 ployed to recognize and sense phosphate with metal ions will be detailed, and their advantages and sh
292  exploited to detect various light and heavy metal ions with a breakthrough detection limit of 50 nM.
293 rdinate all mid-to-late first-row transition-metal ions with high affinity.
294 TOFs) up to 560 s(-1) and those that oxidize metal ions with low TOFs, ~1 s(-1) or less.
295 he contributions of specific interactions of metal ions with monomeric Abeta to their effects on bulk
296 ithin a self-assembled cage composed of four metal ions with six identical antiaromatic walls.
297 al selectivity for Gd(3+) over physiological metal ions with strong translational potential in facili
298 terspersing coordination sites for different metal ions within an artificial molecular strand enables
299                                 However, the metal ions within biolattices and the submicrometer dime
300 mer design because one ligand binds multiple metal ions, yielding bonds of different strengths.

 
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