2022
DOI: 10.1039/d1cp04307b
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Binding of toluidine blue-myristic acid derivative to cucurbit[7]uril and human serum albumin: computational and biophysical insights towards a biosupramolecular assembly

Abstract: A new toluidine blue-myristic acid photosensitizer derivate (TBOMyr) was investigated as a design molecule to bind simultaneously to cucurbit[7]uril (CB[7]) and human serum albumin (HSA) with the aim of constructing...

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Cited by 3 publications
(1 citation statement)
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“…The nature of molecular docking between a biological receptor and a specific substrate involves a molecular recognition process [11][12][13][14][15][16] that is primarily driven by the specific structural and chemical properties of biological receptors: (a) the biological receptor typically has a cavity shape, providing an ideal environment for substrate binding and (b) amino acid residues [17][18][19] within the biological receptor cavity efficiently interact with functional groups of the substrate through non-covalent interactions such as hydrogen bonding [20][21][22] . Inspired by biological receptors, numerous supramolecular macrocycles were studied through conventional molecular docking by using computational and simulation methods [23][24][25][26][27] . Prominent examples of such supramolecular macrocycles include cucurbiturils [28][29][30][31][32][33] and pillar[n]arenes [34][35][36][37][38][39] , which exhibit exceptional host-guest binding capabilities due to their well-defined and complementary structures that can effectively encapsulate and interact with specific guest molecules.…”
mentioning
confidence: 99%
“…The nature of molecular docking between a biological receptor and a specific substrate involves a molecular recognition process [11][12][13][14][15][16] that is primarily driven by the specific structural and chemical properties of biological receptors: (a) the biological receptor typically has a cavity shape, providing an ideal environment for substrate binding and (b) amino acid residues [17][18][19] within the biological receptor cavity efficiently interact with functional groups of the substrate through non-covalent interactions such as hydrogen bonding [20][21][22] . Inspired by biological receptors, numerous supramolecular macrocycles were studied through conventional molecular docking by using computational and simulation methods [23][24][25][26][27] . Prominent examples of such supramolecular macrocycles include cucurbiturils [28][29][30][31][32][33] and pillar[n]arenes [34][35][36][37][38][39] , which exhibit exceptional host-guest binding capabilities due to their well-defined and complementary structures that can effectively encapsulate and interact with specific guest molecules.…”
mentioning
confidence: 99%