2019
DOI: 10.1016/j.procbio.2019.05.009
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The effect of the chelator characteristics on insulin adsorption in immobilized metal affinity chromatography

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Cited by 32 publications
(14 citation statements)
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“…High specificity [12] Powerful tool for analyzing membrane proteins, histidine-tagged proteins, and phosphorylated proteins by using single-step purification [12] procedures [12] easy preparation [13] high adsorption capacity [13], high stability [13] Combined with MALDI-TOF MS detection, high sensitivity detection is achieved [14] The coordination can be reversed by separating the bound proteins using competing ligands (eg imidazole) [15] Glycopeptides and phosphopeptides can be captured simultaneously, by combining with other mechanisms such as HILIC, MOAC [9] No biospecific interaction [16] Many proteins do not have metal affinity [16] Destabilization of purified protein solution due to metal ions [16] Care should be taken when using chelating agents such as EDTA, as it can strip metal ions off the surface [17] Metal oxide affinity chromatography (MOAC)…”
Section: Techniquesmentioning
confidence: 99%
See 1 more Smart Citation
“…High specificity [12] Powerful tool for analyzing membrane proteins, histidine-tagged proteins, and phosphorylated proteins by using single-step purification [12] procedures [12] easy preparation [13] high adsorption capacity [13], high stability [13] Combined with MALDI-TOF MS detection, high sensitivity detection is achieved [14] The coordination can be reversed by separating the bound proteins using competing ligands (eg imidazole) [15] Glycopeptides and phosphopeptides can be captured simultaneously, by combining with other mechanisms such as HILIC, MOAC [9] No biospecific interaction [16] Many proteins do not have metal affinity [16] Destabilization of purified protein solution due to metal ions [16] Care should be taken when using chelating agents such as EDTA, as it can strip metal ions off the surface [17] Metal oxide affinity chromatography (MOAC)…”
Section: Techniquesmentioning
confidence: 99%
“…Here, the basic interactions between the target biomolecule and the affinity sorbent are also listed for each chromatographic method. The most common advantages and disadvantages of these methods are comparatively documented in Table 1 [9,12–41]. The information presented in Figure 2 and Table 1 can be used as a starting point for the selection of an appropriate chromatographic method for a certain biomolecule that is isolated or enriched from a complex biological sample.…”
Section: Bioaffinity Chromatography Techniquesmentioning
confidence: 99%
“…Langmuir model specifically describes the homogeneous and monolayer adsorption on fixed adsorption sites (Kireç et al 2021). Freundlich model assumes the heterogeneous multilayer adsorption on different surface energies (Erol et al 2019a(Erol et al , 2019b Meanwhile, Temkin isotherm model describes that the heat of adsorption decreases with the adsorption coverage due to the adsorbent-adsorbate interactions (Bahrudin et al 2019). The non-linear expressions of Langmuir (Langmuir 1918), Freundlich (Freundlich 1906), and Temkin (Temkin 1940) isotherms are given in Equations ( 7)-( 9), respectively as follows:…”
Section: Isotherm Modelingmentioning
confidence: 99%
“…Magnitude of the magnetic field and the temperature of the material produce diverse spin orientations. The g factor, the spectroscopic cleavage, is calculated according to the following equation [41].…”
Section: Characterization Of the Adsorbentsmentioning
confidence: 99%