2015
DOI: 10.1002/bio.3012
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Fluorescence resonance energy transfer between bovine serum albumin and fluoresceinamine

Abstract: Physical binding-mediated organic dye direct-labelling of proteins could be a promising technology for bio-nanomedical applications. Upon binding, it was found that fluorescence resonance energy transfer (FRET) occurred between donor bovine serum albumin (BSA; an amphiphilic protein) and acceptor fluoresceinamine (FA; a hydrophobic fluorophore), which could explain fluorescence quenching found for BSA. FRET efficiency and the distance between FA and BSA tryptophan residues were determined to 17% and 2.29 nm, r… Show more

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Cited by 29 publications
(14 citation statements)
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References 36 publications
(42 reference statements)
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“…A slight blue shift of 1 nm in the fluorescence peak of BSA in presence of QDs as compared to the spectrum of BSA alone, is observed as the concentration of CdTe QDs gradually increases. This variation in the characteristic fluorescence peak of BSA indicates the interaction occurring between BSA and CdTe QDs …”
Section: Resultsmentioning
confidence: 97%
See 1 more Smart Citation
“…A slight blue shift of 1 nm in the fluorescence peak of BSA in presence of QDs as compared to the spectrum of BSA alone, is observed as the concentration of CdTe QDs gradually increases. This variation in the characteristic fluorescence peak of BSA indicates the interaction occurring between BSA and CdTe QDs …”
Section: Resultsmentioning
confidence: 97%
“…Within the family of serum albumins, BSA is used as a model in studying protein‐ligand binding and has 76% sequence homology with human serum albumin (HSA) . BSA has three intrinsic fluorophores–tryptophan (Trp), tyrosine (Tyr) and phenylalanine (Phe).…”
Section: Introductionmentioning
confidence: 99%
“…We then decided to exemplify this reaction to other aromatic amines, including a few that are included in compounds of biological interest. We have studied the reactivity of Boc‐Gly‐Bt 11 with both 7‐amino‐4‐methylcoumarin (AMC) 12 , and fluoresceinamine 13 , which are used for the synthesis of fluorescent probes (Scheme ) , . These syntheses are often quite complicate and generally led to the expected compounds in low yields , …”
Section: Resultsmentioning
confidence: 99%
“…The hydrogen bonds can be formed between the dense carboxylic groups on the backbone of the AP and most of amino groups on the surface of BSA proteins. For studying the conformational information of proteins, three dimensional fluorescence spectroscopy (3DFS) is a facile and powerful method to provide more detailed information about the conformational and micro-environmental changes of protein that combined with molecules [35,42].…”
Section: Study On the Binding Mechanism By Fluorescence Quenchingmentioning
confidence: 99%