2014
DOI: 10.1016/j.bmcl.2014.04.096
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Design of a binuclear Ni(II)–iminodiacetic acid (IDA) complex for selective recognition and covalent labeling of His-tag fused proteins

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Cited by 17 publications
(12 citation statements)
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“…3A). If the C-terminal 6×His-tag of the connector is facing the trans-chamber, the electron donor groups on histidine imidazole rings will readily form coordinate bonds with the Ni-NTA complex on nanogold (K D of 390 nM) [37; 38]. …”
Section: Resultsmentioning
confidence: 99%
“…3A). If the C-terminal 6×His-tag of the connector is facing the trans-chamber, the electron donor groups on histidine imidazole rings will readily form coordinate bonds with the Ni-NTA complex on nanogold (K D of 390 nM) [37; 38]. …”
Section: Resultsmentioning
confidence: 99%
“…You and co-workers also studied portions of brain tissue (hypothalamus, hippocampus, cortex, and amygdala). They found that the ratio of 31 P/ 66 Zn decreased beyond tumor limits, indicating that variations in this ratio can be used to distinguish healthy vs. cancerous tissue [14].…”
Section: Significance Development and Challenges In The Detection Omentioning
confidence: 99%
“…Aside from these interferences, the sensing results were influenced by the other factors such as the environment of the system including solvent used, type and pH of the buffer, the concentration of Zn 2+ ions present compared to the other ions, solubility properties, and of course, the characteristic and behavior of the probe itself. They are so many receptors used as fluorophore as binding sites such as di-2picolylamine (DPA) [55,56] quinoline [57,58], bipyridine [59][60][61][62], acyclic and cyclic polyamines [63,64], iminodiacetic acid [65,66], triazole [67][68][69], and Schiff-base receptors [70] ( Figure 1). However, it is necessary to notice that few compounds fluoresce by itself or fluoresce after the interaction with the target.…”
Section: Quinoline and Derivatives For Zn 2+ Fluorophoresmentioning
confidence: 99%
“…Immobilized metal ion affinity chromatography (IMAC) is an ideal technique for immobilizing and purifying proteins with poly-histidine tags. [9][10][11] IMAC immobilized transition-metal ions (Cu 2+ , Ni 2+ , Co 2+ , Zn 2+ ) via ligands such as one tridentate iminodiacetic acid (IDA), [12][13][14] two tetradentates nitrilotriacetic acid (NTA), [15][16][17] carboxymethylated aspartic acid (CM-Asp), 18,19 pentadentate tris (carboxymethyl) ethylenediamine (TED). 20,21 Specic interactions between transition-metal ions and polyhistidine tags (his-tags) on the N-or C-terminals of proteins facilitate protein separation and purication under different ionic strength and pH of solutions.…”
Section: Introductionmentioning
confidence: 99%