Design and Synthesis of a Peptidyl-FRET Substrate for Tumor Marker Enzyme human Matrix Metalloprotease-2 (hMMP-2)-Reference-Cited by-同舟云学术

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Design and Synthesis of a Peptidyl-FRET Substrate for Tumor Marker Enzyme human Matrix Metalloprotease-2 (hMMP-2)

Published:2012-03-11 Issue:3 Volume:18 Page:207-215
ISSN:1573-3149
Container-title:International Journal of Peptide Research and Therapeutics
language:en
Short-container-title:Int J Pept Res Ther

Author:

Alam Mehtab,Ali Syed Abid,Abbasi Atiya,Kalbacher Hubert,Voelter Wolfgang

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Molecular Medicine,Biochemistry,Bioengineering,Analytical Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s10989-012-9293-0.pdf

Reference46 articles.

1. Beekman B, Wouter J, Bloemhoff W, Ronday K, Tak PP, te Koppele JM (1996) Convenient fluorometric assay for matrix metalloproteinase activity and its application in biological media. FEBS Lett 390:221–225

2. Bickett DM, Green MD, Berman J, Dezube M, Howe AS, Brown PJ, Roth JT, McGeehan GM (1993) A high throughput fluorogenic substrate for interstitial collagenase (MMP-1) and gelatinase (MMP-9). Anal Biochem 212:58–64

3. Buchardt J, Ferreras M, Krog-Jensen C, Delaisse JM, Foged NT, Meldal M (1999) Phosphinic peptide matrix metalloproteinase-9 inhibitors by solid-phase synthesis using a building block approach. Chem Eur J 5:2877–2884

4. Buchardt J, Schiodt CB, Krog-Jensen C, Delaissé JM, Foged NT, Meldal M (2000) Solid phase combinatorial library of phosphinic peptides for discovery of matrix metalloproteinase inhibitors. J Comb Chem 2:624–638

5. Chen X, Kalbacher H, Gründer S (2005) The tarantula toxin psalmotoxin 1 inhibits acid-sensing ion channel (ASIC) 1a by increasing its apparent H+ affinity. J Gen Physiol 126:71–79

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