2007
DOI: 10.1002/anie.200702399
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Cleavage Agents for Soluble Oligomers of Amyloid β Peptides

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Cited by 111 publications
(89 citation statements)
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“…It seems that the future applications of metal assisted peptide bond hydrolysis in biotechnology belong to the latter two approaches, if their weak points will be overcome. There is also some promise in the cyclen complexes, especially in their most recent applications for amyloid digestion [134][135][136][137].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…It seems that the future applications of metal assisted peptide bond hydrolysis in biotechnology belong to the latter two approaches, if their weak points will be overcome. There is also some promise in the cyclen complexes, especially in their most recent applications for amyloid digestion [134][135][136][137].…”
Section: Discussionmentioning
confidence: 99%
“…In another development of the work on cyclen complexes by Suh and coworkers several libraries of Co(III) complexes were designed, synthesized, and derivatized on the cyclen frame [134][135][136]. Several complexes were active against soluble oligomers of human amyloidogenic peptides: the Alzheimer's Disease A␤(1-42) peptide, human islet amyloid polypeptide (h-IAPP) related to type 2 diabetes and ␣-synuclein, related to Parkinson's Disease.…”
Section: Practical Applications Of Metal-assisted Peptide Bond Hydrolmentioning
confidence: 99%
“…13 The Co(III) complexes of A and B were prepared according to the method reported previously. 7,[9][10][11]15 The substrate proteins were obtained from Sigma. Rate measurements carried out as reported previously.…”
Section: Methodsmentioning
confidence: 99%
“…[2][3][4][5][6][7][8][9][10][11] Proteolytic activity of the Cu(II) complex (Cu(II)cyclen) of cyclen was greatly enhanced on attachment to polystyrene backbone apparently due to the hydrophobic microenvironment.…”
mentioning
confidence: 99%
“…4 As a new therapeutic option for amyloidoses, we have proposed reduction of the level of the pathogenic oligomers of AmPs through peptide cleavage. 1,2,7 As shown in Figure 1 where the cleavage agent is indicated as (R)-(LCo III ), cleavage of an AmP included in a target oligomer reduces the concentration of the target oligomer, leading to decreases in the concentrations of other oligomers which readily transform into the target oligomer.…”
mentioning
confidence: 99%