2006
DOI: 10.1002/chem.200600148
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Diels–Alder Ligation of Peptides and Proteins

Abstract: It is worth while, all,If the soul is not small.

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Cited by 84 publications
(53 citation statements)
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References 119 publications
(164 reference statements)
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“…The Diels-Alder reaction has been presented as an elegant chemoselective methodology to introduce fluorescent labels on proteins, [23][24][25][26][27][28][29][30][31] to prepare neo-glycoproteins, [32] or to chemically activated proteins. [33][34][35] Waldmann et al have applied the Diels-Alder cycloaddition as a new way to label proteins with fluorophores in vitro.…”
Section: Site-directed Chemical Modification Of Proteins By Diels-aldermentioning
confidence: 99%
See 1 more Smart Citation
“…The Diels-Alder reaction has been presented as an elegant chemoselective methodology to introduce fluorescent labels on proteins, [23][24][25][26][27][28][29][30][31] to prepare neo-glycoproteins, [32] or to chemically activated proteins. [33][34][35] Waldmann et al have applied the Diels-Alder cycloaddition as a new way to label proteins with fluorophores in vitro.…”
Section: Site-directed Chemical Modification Of Proteins By Diels-aldermentioning
confidence: 99%
“…[33][34][35] Waldmann et al have applied the Diels-Alder cycloaddition as a new way to label proteins with fluorophores in vitro. [23] Streptavidin -composed of four biotin-binding subunits -was acylated with a hexadienyl bifunctional linker 1 on a lysine side chain. The diene-modified protein 2 was Scheme 2. subjected to Diels-Alder ligation with three different fluorescent labeled maleimide compounds 3, 4 and 5, in water and room temperature respectively.…”
Section: Site-directed Chemical Modification Of Proteins By Diels-aldermentioning
confidence: 99%
“…Diels-Alder (DA) reactions have also been investigated for various biological applications due to their high yields, specific reaction (between a diene and a dienophile) that occurs in mild aqueous conditions. 226,227 No catalysts are required for the reaction and it produces no byproducts. Recently, a DA reaction-based bioconjugated HA hydrogel was characterized by Tan et al 228 Although the gels are biocompatible and degradable, the gels required over 20 min to set and reached a storage modulus under 20 Pa, which is very weak.…”
Section: Schiff Base-mediated Gelationmentioning
confidence: 99%
“…128 Furthermore, the nonspecific conjugation of cyclooctynes to the thiols of Cys containing proteins can be significant. 152,[155][156][157][158][159][160][161][162][163][164][166][167][168][169] The inverse electron-demand Diels-Alder reaction between a strained alkene like norbornene or trans-cyclooctyne and a tetrazine is also an alternative for bioconjugations. 126,166 The tetrazine dienophile of these cycloadditions is also…”
mentioning
confidence: 99%
“…[167][168][169] Furthermore, the complicated synthesis of tetrazine and trans-cyclooctyne reagents inhibits their widespread application in bioconjugations. 160,161,170 Since cholesterol can be applied as a protein membrane delivery vector, it suggests another application for introducing a bioorthogonal function to the plasma membrane of live cells.…”
mentioning
confidence: 99%