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1 hat the nature of nfGNPs-VLPs interaction is non-covalent.
2  indicating that the dominant interaction is non-covalent.
3 s diverse field with a focus on covalent and non-covalent 2D polymers and frameworks, and self-assemb
4 horesis studies demonstrate the formation of non-covalent adducts with natural plasmids.
5 rmal properties, low chemical reactivity and non-covalent affinity to graphene enable transfer of wri
6 gonists, did not affect sensitisation by the non-covalent agonist carvacrol, which activates by bindi
7           Here, we report the discovery of a non-covalent agonist, GNE551, and determine a cryo-EM st
8                                          How non-covalent agonists activate the channel and whether c
9 ctivate the channel and whether covalent and non-covalent agonists elicit the same physiological resp
10  action of the agonist, because covalent and non-covalent agonists were equally effective, and is lon
11 77 nM, which places it among the most potent non-covalent AmpC inhibitors known.
12                   Supramolecular copolymers, non-covalent analogues of synthetic copolymers, constitu
13  In particular, this review analyzes various non-covalent and covalent interactions and chemistry app
14                    This review is focused on non-covalent and covalent interactions that are employed
15                           The interaction is non-covalent and extraction with octanol completely remo
16  meditope peptides could be used as specific non-covalent and paratope-independent handles in targete
17 d from a non-expert perspective, to identify non-covalent and pre-associative nucleic acid recognitio
18                                      Here, a non-covalent approach was used to conjugate PEG bearing
19     The use of ionic self-assembly, a facile non-covalent approach, to access non-conventional block
20 he supramolecular complexation behaviour and non-covalent approaches rather than on the proposed appl
21 e chemically modified, by either covalent or non-covalent approaches, in order to interface them with
22 ce of electronic properties not evidenced in non-covalent assemblies.
23 at a temperature (371 K) where the pristine, non-covalent assembly exists exclusively in a molecularl
24 nergy when compared to that recorded for the non-covalent assembly.
25                                           By non-covalent association after proteolytic cleavage, the
26 -specific chemisorption of MTFP and multiple non-covalent attractive interactions between the carbony
27 petition between electrostatic repulsion and non-covalent attractive interactions.
28                          Interestingly, when non-covalent backside ubiquitin binding cannot occur, th
29 caffold for molecular transport based on its non-covalent base pairing to assemble both stationary an
30 ompared to native beta-Lactoglobulin and the non-covalent beta-lactoglobulin/caffeic complex (betaLg/
31              Also, due to the ability of the non-covalent beta-sheet cross-links to reassemble, the h
32  antibodies and DNA, which undergo important non-covalent binding interactions, with the formation of
33 strategies to fortify their capsids, such as non-covalent binding of auxiliary 'decoration' (Dec) pro
34                                              Non-covalent binding of K63-Ubn to 2CARD induces its tet
35               The biological implications of non-covalent binding of polyphenols to BLG were investig
36 o design ADCs that self-assemble through the non-covalent binding of the antibody to a payload that w
37 ing sites for allicin, whereas the number of non-covalent binding sites increased for diallyl disulfi
38 d gas diffusion electrodes (GDEs) by using a non-covalent binding strategy.
39 terized by two key molecular properties: (1) non-covalent binding to an antibody-based therapeutic, a
40                       However, the effect of non-covalent binding to Nedd8 remains unknown.
41 1p and E3 components to the E2p core through non-covalent binding.
42 s a consequence of blocking the stimulatory, non-covalent, binding of ubiquitin to the backside of Ub
43     Thus, bPoNAs can serve as tools for both non-covalent bioconjugation and structure-function nucle
44 em prime candidates for in vitro and in vivo non-covalent bioconjugation, for imaging and delivery ap
45 tibody and the intermediate affinity of this non-covalent bond, fully assembled probes do not aggrega
46  achieved in dynamic reversible covalent and non-covalent bonding chemistries for self-healing polyme
47  Waals radii) and its ability to form strong non-covalent bonding interactions with pi-electron-rich
48 ployed to elucidate thermodynamic behaviors, non-covalent bonding of coacervates, and microstructure
49  the hydrophobicity of the protein such that non-covalent bonding within network was modified.
50              This tutorial review summarizes non-covalent bonding, reversible reactions and responsiv
51                                          The non-covalent bonds allow the extrusion of the inks into
52 rate shear forces that exceed the ability of non-covalent bonds to remain attached.
53                                              Non-covalent bonds, more likely salt bridge and ionic in
54               We also demonstrate how strong non-covalent bonds, which are versatile for controlled p
55                                          The non-covalent capture of olive pheromones inside the beta
56 s has been performed under both covalent and non-covalent catalysis, with diaryl prolinols, imidazoli
57 at phenolics may complex with starch through non-covalent CH-pai bonds along alpha-(1 -> 4) glycosidi
58  interactions contribute to the formation of non-covalent chainmail in BPP-1, unlike covalent inter-p
59         The idea I advocate here is that the non-covalent change in protein conformation itself might
60 ry and the emergence of dynamic covalent and non-covalent chemistries, novel perspectives have been o
61      While, initial recruiters have utilized non-covalent chemistry for protein binding, very recentl
62                 However, the contribution of non-covalent chromatin structure to the poised state is
63 tion in mesostructured soft solids involving non-covalent co-assembly has received little attention.
64 olution on how the monomer structure affects non-covalent COF layer stacking.
65                          The straightforward non-covalent combination of MSN and gold-protein cluster
66 , the intracellular delivery of avidin, as a non-covalent complex with a biotinylated Tat vector, is
67 ivery capabilities and function by forming a non-covalent complex with cargo, protecting it from nucl
68  and finally dynamic molecular motion within non-covalent complexes as unravelled by hydrogen-deuteri
69 that CB[7]6 is among the tightest monovalent non-covalent complexes ever reported in water with Ka =7
70                                          The non-covalent complexes formed between the peptide and ca
71                    Several new structures of non-covalent complexes of PGA with different substrates,
72 sociation and formation of covalent bonds in non-covalent complexes through the reactivity in the res
73                                Moreover, the non-covalent complexes were optimally detected at wavele
74 heir ability to specifically target and form non-covalent complexes with other proteins.
75                The array is fabricated using non-covalent conjugation of an aptamer-anchor polynucleo
76  tunable biohybrid hydrogels by covalent and non-covalent conjugation schemes, including both theory-
77                            Here we show that non-covalent contacts between the active molecular compo
78 tructures, we uncover a conserved network of non-covalent contacts that defines the GPCR fold.
79 ages as well as challenges relative to their non-covalent counterpart.
80 differences: the chains are kinked, enabling non-covalent cross-linking of fibrils and disfavoring fo
81 lf-assembling beta-sheet peptides to provide non-covalent cross-linking through beta-sheet assembly,
82 s with mucin forming a network structure via non-covalent cross-links between mucin chains.
83 d with a small-amount dynamic CB[8]-mediated non-covalent crosslinking (2.5 mol%), yields extremely s
84                                        These non-covalent crosslinking moieties are able to undergo a
85 oducing chemical moieties to promote dynamic non-covalent crosslinking of the conjugated polymers.
86                                     Specific non-covalent crosslinks involving domains/motifs lead to
87 s and / or domains that can form reversible, non-covalent crosslinks with one another.
88                                 However, the non-covalent Cu(II) coordination approach is vulnerable
89 main cysteines, retained the ability to form non-covalent dimers, and all of the BST-2 variants were
90 oluble and membrane-bound proteins exists as non-covalent dimers, trimers, and higher-order oligomers
91                             The formation of non-covalent directional interactions, such as hydrogen
92 (AH78 TriplatinNC) and 7 (AH78H), are potent non-covalent DNA binding agents where nucleic acid recog
93    There is a wide range of applications for non-covalent DNA binding ligands, and optimization of su
94 chanisms, we have successfully constructed a non-covalent DNA catalysis network that resembles an all
95 ctive is provided along with descriptions of non-covalent DNA recognition focusing on intercalation,
96                                     (b) Some non-covalent drug-protein complexes rely on rather affin
97              In the present communication, a non-covalent fenarimol-imprinted polymer was synthesized
98 e interactions by docking, both covalent and non-covalent, for 38 lipases with a large number of stru
99 to use supramolecular design to leverage the non-covalent forces between COF monomers and sheets to i
100 ecular polymers depending on the cooperative non-covalent forces driving their formation, with partic
101 ulsive steric and stabilizing intermolecular non-covalent forces in the stereodetermining hydride tra
102  of n-->pi* interactions in the inventory of non-covalent forces that contribute to protein stability
103 oups that may interact either by covalent or non-covalent forces with other molecules present in the
104  whereas octanal bound PPIs via covalent and non-covalent forces.
105 onds which are then stacked together through non-covalent forces.
106 t inhibitors through merging of covalent and non-covalent fragment hits; one series of low-reactivity
107 med a large-scale screen of electrophile and non-covalent fragments through a combined mass spectrome
108 nt synthetic approaches for the covalent and non-covalent functionalization and characterization of G
109                                          The non-covalent functionalization through pi-pi stacking in
110                                              Non-covalent functionalization with phospholipid-polyeth
111  into organophilic material via covalent and non-covalent grafting strategies.
112 rovide new insights into the role of unusual non-covalent halogen bonding interactions involved in th
113                              Contrary to the non-covalent heterogeneous dispersion of pure (unmodifie
114                                The resulting non-covalent heterotrimer was exported in a Tat-dependen
115 that the molecular self-assembly in water by non-covalent host-guest molecular recognition is suffici
116  successful supramolecular polymerization by non-covalent host-guest molecular recognition was confir
117 thylene glycol interact with heparin to form non-covalent hydrogels.
118  associations are stabilized and mediated by non-covalent hydrogen bonds that arise on the backbone o
119 chains into a short polymer block leading to non-covalent, hydrophobic interactions with the lipid bi
120  such selectivity is partially retained upon non-covalent (i.e. intercalation) mixture formed by nati
121 tion interface was fabricated via simple and non-covalent immobilization of antibody using lectin-med
122                                The method of non-covalent immobilization of DNA probes on an uncharge
123 /Au/GO nanocomposite was synthesized through non-covalent imprinting process in the presence of IMQ,
124 enetic or chemical modification, we report a non-covalent infusion technique that facilitates efficie
125                             K27 is a potent, non-covalent inhibitor of nucleotide exchange, showing c
126 ailed interactions between first generation, non-covalent inhibitors and GlgE, a variant Streptomyces
127 o generate potent, class-specific, bioactive non-covalent inhibitors for these enzymes are still limi
128 to advance the development of high affinity, non-covalent inhibitors of K-Ras oncogenic mutants.
129 ve cells using either covalent attachment or non-covalent insertion, while maintaining high cell viab
130 lographically observed structural motifs and non-covalent interaction acceptor-donor pairings.
131                       We found an unexpected non-covalent interaction between AbDsbA and the highly c
132 ELF domain of FANCL is required to mediate a non-covalent interaction between FANCL and ubiquitin.
133 vity and/or selectivity have been imputed to non-covalent interaction between the reaction partners.
134 ting evidence points to the emerging role of non-covalent interaction between ubiquitin and the targe
135 as been a growing interest in exploring this non-covalent interaction in nanoscale drug delivery syst
136 driver for assembly, the contribution of the non-covalent interaction is to direct the molecular-leve
137 nidine and arginine formed both covalent and non-covalent interaction products.
138 s occurs via an initial metal ion-dependent, non-covalent, interaction between TSG-6 and HCs that als
139  The pretargeting approach utilises specific non-covalent interactions (e.g. strept(avidin)/biotin) o
140 n of the major enantiomer through attractive non-covalent interactions (NCIs) rather than retarding t
141 ondary orbital interactions, are overcome by non-covalent interactions affording to the unusual exo a
142       In natural systems, highly synergistic non-covalent interactions among biomolecular components
143 d crystalline molecules are organized due to non-covalent interactions and due to delicate nature of
144  achieved a predictable control over various non-covalent interactions and have used these weak inter
145 r the rational manipulation of these complex non-covalent interactions and their direct incorporation
146 ly of low-molecular weight compounds by weak non-covalent interactions and thus, they may be easily d
147                                              Non-covalent interactions are thought to be involved in
148                     Nature uses the power of non-covalent interactions as the basis for many kinds of
149 s tools for the qualitative understanding of non-covalent interactions as well as energy decompositio
150 or two diverse catalytic systems with unique non-covalent interactions at the heart of each process.
151  adhesive materials that rely on a number of non-covalent interactions at the interfaces.
152 fers enormous potential, in which attractive non-covalent interactions between a chiral catalyst and
153 the channel protein through a combination of non-covalent interactions between adjacent helices and c
154 vantage of the cumulative effect of multiple non-covalent interactions between adjacent molecules.
155                                              Non-covalent interactions between beta-lactoglobulin (BL
156              The theoretical analysis of the non-covalent interactions between host and guest confirm
157 s that are loaded onto nanoparticles through non-covalent interactions between polyhistidine tags and
158       In this work, substituent effects tune non-covalent interactions between side-chain fluorinated
159 hat the amide E:Z equilibrium is affected by non-covalent interactions between the amide oxygen and a
160  of viral capsid self-assembly require weak, non-covalent interactions between the capsid subunits to
161                                              Non-covalent interactions between the cellulose crystals
162  be dedicated to catalytic systems for which non-covalent interactions between the partners of the re
163 standing of the synergy between covalent and non-covalent interactions can form the basis for any pre
164 ssembly of binary systems driven by specific non-covalent interactions can greatly expand the structu
165 ous assembly driven by coordination multiple non-covalent interactions can help explain the well-orde
166 and consolidated by the recruitment of other non-covalent interactions contributed by subsurface moie
167 nt proteins provide striking examples of how non-covalent interactions could be exploited for tuning
168 logy is validated by directly connecting the non-covalent interactions defined through empirical data
169                                     Stronger non-covalent interactions delayed pepsin and pancreatin
170 rotein analysis due to its ability to retain non-covalent interactions during measurements, making it
171                           The utilization of non-covalent interactions for the design of adhesives wi
172 w molecular weight gelators (LMWGs) based on non-covalent interactions has been proven to be a useful
173                   In this way, many types of non-covalent interactions have been characterized, from
174 re designed to interact with one another via non-covalent interactions in order to create function.
175 ative enzymes and their models, the roles of non-covalent interactions in promoting this activity are
176 s this, the significantly higher strength of non-covalent interactions in the absence of competing so
177                                  The role of non-covalent interactions in the formation of visco-elas
178 n-biotin interaction is one of the strongest non-covalent interactions in the nature.
179 results more from stabilizing intramolecular non-covalent interactions in the secondary coordination
180     These results indicate that manipulating non-covalent interactions in zein can alter and in some
181                                Commonly used non-covalent interactions include hydrogen bonding, pai-
182 unfolding interest in integrating unorthodox non-covalent interactions into functional systems.
183 racteristics underlying the most significant non-covalent interactions involved in fibrin polymerizat
184  binding and catalysis are often mediated by non-covalent interactions involving aromatic functional
185 lecular chemistry is overwhelmingly based on non-covalent interactions involving organic architecture
186  plasmon resonance (SPR) phenomenon to study non-covalent interactions not just between plasmonic par
187 ells can metabolize aroma compounds and that non-covalent interactions occur between aroma compounds
188 rb on graphitic nanomaterials (GNMs) through non-covalent interactions occurring at their interfaces.
189                                              Non-covalent interactions of EGCG with proteins contribu
190                                        Next, non-covalent interactions of peptides with other peptide
191 tuitive to use it to study the structure and non-covalent interactions of proteins that form in solut
192 pecific, directional, tunable and reversible non-covalent interactions offer unprecedented advantages
193                     They can be as labile as non-covalent interactions or as permanent as covalent bo
194 to their dynamic, stimuli-responsive nature, non-covalent interactions represent versatile design ele
195 terplay between polyvalent electrostatic and non-covalent interactions that work in unison to disrupt
196 iew eminent examples which take advantage of non-covalent interactions to achieve regiocontrol.
197 ry have previously been synthesized by using non-covalent interactions to assemble and entangle molec
198                Supramolecular chemistry uses non-covalent interactions to coax molecules into forming
199 ts a combination of attractive and repulsive non-covalent interactions to direct the enantio-determin
200             This strategy takes advantage of non-covalent interactions to template a topochemical pho
201 ms make simultaneous use of several types of non-covalent interactions together, one would expect the
202 esidue offset is lucrative, as it leaves the non-covalent interactions unsatisfied at the termini and
203 d subsequently quantify the strengths of the non-covalent interactions using Kohn-Sham density functi
204     By establishing conditions that preserve non-covalent interactions we exploit the surface to capt
205 ysis was performed on the complex network of non-covalent interactions which stabilize each cluster.
206 a viral RNA sensor, RIG-I, both covalent and non-covalent interactions with K63-linked ubiquitin chai
207                                              Non-covalent interactions with the -CF(3) groups, and hy
208 olated guest molecules demonstrates that the non-covalent interactions with the host hardly affect th
209 les are assembled into regular structures by non-covalent interactions, attract tremendous interests
210 re the nature of the covalent chemical bond, non-covalent interactions, bond formation, and exotic 3-
211      By using specific, dynamic, and tunable non-covalent interactions, engineered approaches to drug
212 c receptors which bind carbohydrates through non-covalent interactions, mimicking the strategies used
213                                 Furthermore, non-covalent interactions, such as electrostatics, pi-st
214                                              Non-covalent interactions, such as self-interaction and
215 ssociate with the resulting Np complexes via non-covalent interactions, which together decrease the e
216 We found that the structure is stabilized by non-covalent interactions, with dominant contributions f
217 n-2D materials that adhere primarily through non-covalent interactions.
218 ave renewed their interest in water-mediated non-covalent interactions.
219 eine was enclosed within the gel network via non-covalent interactions.
220 ucts and at the same time exhibiting various non-covalent interactions.
221 ing that protein network was mostly based on non-covalent interactions.
222 IP3 R1 remain associated, presumably through non-covalent interactions.
223 ng nanomaterial whose assembly is driven via non-covalent interactions.
224 action partners that can be held together by non-covalent interactions.
225 stic properties of zein arise as a result of non-covalent interactions.
226 plex transformations exploiting covalent and non-covalent interactions.
227 e excited state by employing confinement and non-covalent interactions.
228 nition phenomena are a direct consequence of non-covalent interactions.
229                     Self-assembly occurs via non-covalent interactions.
230 eric structures from small molecules through non-covalent interactions.
231 dapt to cell behavior as a result of dynamic non-covalent interactions.
232 e correlations is introduced for postulating non-covalent interactions.
233          Here we systematically investigated non-covalent interchain interactions for CH3 domains in
234                       Specifically, the weak non-covalent intermolecular interactions induced by the
235 trameric complex exhibits the involvement of non-covalent intermolecular interactions that are locali
236 otein nanostructures have been assembled via non-covalent intramolecular and intermolecular interacti
237 l of photo-activation, enabling the study of non-covalent kinetic intermediates and heterogeneous mix
238 es, the activities of which are regulated by non-covalent ligand binding, and that may provide a temp
239 xes and allows selections in the presence of non-covalent ligands.
240                        The p75(NTR) DD forms non-covalent, low-affinity symmetric dimers in solution.
241                     The kinetic stability of non-covalent macromolecular complexes controls many biol
242 ential benefit of using a serum protein in a non-covalent manner in conjunction with paclitaxel nanoc
243 s can coat the surfaces of Ad particles in a non-covalent manner to modify their transduction propert
244 stabilized by serum protein transferrin in a non-covalent manner.
245 e synthetic biology, nanodisc-technology and non-covalent mass spectrometry provides excellent synerg
246 e not held together by covalent bonds but by non-covalent mechanical interactions.
247 t NAAA in a potent and selective manner by a non-covalent mechanism are described.
248                             Microtubules are non-covalent mesoscale polymers central to the eukaryoti
249 ausible approach to the development of novel non-covalent methods of binding, retention, and release
250             These data demonstrated that our non-covalent modification was able to alter Ad's interac
251 were immobilized to the graphene surface via non-covalent modification.
252 actor governing recognition, particularly in non-covalent molecularly imprinted polymers.
253  compound exemplifies a second generation of non-covalent NAAA inhibitors that may be useful in the t
254  of dynamic features as a consequence of the non-covalent nature of their core interactions, but also
255 inically relevant setting, likely due to the non-covalent nature of their interaction with collagen m
256 both Smurf1 and its homologue Smurf2 carry a non-covalent Nedd8-binding site within its catalytic HEC
257        Responsive graphene oxide sheets form non-covalent networks with optimum rheological propertie
258         If a fusion protein assembles into a non-covalent oligomeric complex, exciting their GFP moie
259 k using pyrene carboxylic acid (PCA) through non-covalent pai-pai stacking interaction between PCA an
260                   We describe seven kinds of non-covalent-pai interactions between c-di-AMP and its r
261           This is the first demonstration of non-covalent PEGylation of acylated peptides, an importa
262 , phospholipids (dithranol, THAP, HABA), and non-covalent peptide-peptide and protein-peptide complex
263 advance for future structure-based design of non-covalent peptidomimetic inhibitors.
264                                              Non-covalent pi-pi interactions are central to chemical
265 ustering by enabling reversible, cooperative non-covalent (pi-pi, solvophobic, and hydrogen bonding)
266 MO-interacting motif favors formation of the non covalent PIAS1.SUMO.UBC9 ternary complex.
267                                            A non-covalent polymerization reaction between macromolecu
268                               In this study, non-covalent polymers from self-assembled boric acid wer
269                        Surface coating using non-covalent polymers from self-assembled boric acid wil
270                                              Non-covalent polymers have remarkable advantages over sy
271 l properties of formally substitution-inert "non-covalent" polynuclear platinum complexes (PPCs).
272 e of the polysaccharides by the formation of non-covalent polysaccharides-OE complexes.
273                               We introduce a non-covalent pore engineering approach to achieve except
274 uctural proteomics under the assumption that non-covalent protein complexes being transferred into th
275  moieties in these polymeric mimics improves non-covalent protein delivery, providing crucial design
276                          Rationally designed non-covalent protein nanocapsules incorporating copper-f
277                  In this tutorial review the non-covalent recognition of CWAs is considered from firs
278 shed a mechanism-of-action involving initial non-covalent recognition of inhibitors at the IspD bindi
279  for mediating targeted cell penetration and non-covalent self-assembly with therapeutic cargo, formi
280                                     Numerous non-covalent small-molecule Keap1-Nrf2 PPI inhibitors ha
281 ierarchical functional nanomaterials through non-covalent soft-chemical routes.
282 , supramolecular structures held together by non-covalent solvophobic and coordination interactions a
283 cond conformational change associated with a non-covalent step not previously reported for Pol beta.
284           The second part introduces various non-covalent strategies for achieving desired doping in
285 analysis suggested covalent (ester bond) and non-covalent (strong hydrogen-bonding, mostly) interacti
286 exity of the extracellular matrix (ECM) to a non-covalent structure with minimal chemically defined c
287 "strands"-connected together via covalent or non-covalent/supramolecular interactions, are arguably t
288 essing challenges in the prospering field of non-covalent surface functionalization.
289    The overall approach offers an efficient, non-covalent synthesis method for the solution-phase fab
290 des an attractive bottom-up approach for the non-covalent synthesis of nascent axial organic heterost
291 ning self-assembled structure in biology and non-covalent synthesis.
292 her differentiation in terms of covalent and non-covalent systems.
293  Finally, our results also indicate that the non-covalent ternary complex is required for the known t
294  as assembled into a previously unidentified non-covalent ternary complex with SUMO as evidenced by b
295                                         This non-covalent three-helix bundle domain is homologous in
296 either covalent arabinogalactan mycolates or non-covalent trehalose mycolates in live mycobacteria.
297 mology domain (THD) of human (h)4-1BBL forms non-covalent trimers, we found that m4-1BBL formed a cov
298                                              Non-covalent Ub binding to the backside of certain E2s p
299 nexpected synergism between the covalent and non-covalent ubiquitin interaction modes.
300                                              Non-covalent vdW interactions, however, are ubiquitous i

 
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