WeightNameValue
1000 Titel
  • Extra- and Intracellular Imaging of Human Matrix Metalloprotease 11 (hMMP-11) with a Cell-penetrating FRET Substrate
1000 Autor/in
  1. Meyer, B. Sina |
  2. Rademann, Jörg |
1000 Erscheinungsjahr 2012
1000 LeibnizOpen
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2012-08-27
1000 Erschienen in
1000 Quellenangabe
  • 287: 37857-37867
1000 FRL-Sammlung
1000 Verlagsversion
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488058/ |
  • http://doi.org/10.1074/jbc.M112.371500 |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Matrix metalloprotease 11 (MMP-11), a protease associated with invasion and aggressiveness of cancerous tissue, was postulated as a prognostic marker for pancreatic, breast, and colon cancer patients. Expression analysis, however, did not reveal localization and regulation of this protease. Thus, cellular tools for the visualization of MMP-11 are highly desirable to monitor presence and activity and to elucidate the functional role of MMP-11. Therefore, fluorescein-Dabcyl-labeled Foerster resonance energy transfer (FRET) substrates were developed. The design focused on enhanced peptide binding to human MMP-11, employing an unusual amino acid for the specificity pocket P1′. The addition of several arginines resulted in a cell-permeable FRET substrate SM-P124 (Ac-GRRRK(Dabcyl)-GGAANC(MeOBn)RMGG-fluorescein). In vitro evaluation of SM-P124 with human MMP-11 showed a 25-fold increase of affinity (kcat/Km = 9.16 × 103 M−1 s−1, Km = 8 μM) compared with previously published substrates. Incubation of pancreatic adenocarcinoma cell line MIA PaCa-2 and mamma adenocarcinoma cell line MCF-7 with the substrate SM-P124 (5 μM) indicated intra- and extracellular MMP-11 activity. A negative control cell line (Jurkat) showed no fluorescent signal either intra- or extracellularly. Negative control FRET substrate SM-P123 produced only insignificant extracellular fluorescence without any intracellular fluorescence. SM-P124 therefore enabled intra- and extracellular tracking of MMP-11-overexpressing cancers such as pancreatic and breast adenocarcinoma and might contribute to the understanding of the activation pathways leading to MMP-11-mediated invasive processes.
  • CAPSULE: BACKGROUND: Matrix metalloprotease 11 induces tumorigenesis and promotes invasive tissue behavior. Its function is hardly understood. RESULTS: MMP-11 activatable cell-permeable FRET substrates were developed and tested in vitro, visualizing MMP-11 activity. CONCLUSION: Rational design of FRET substrates yielded new imaging tools for MMP-11. SIGNIFICANCE: MMP-11 imaging can assist functional studies, investigating native substrates, or interaction partners of MMP-11.
1000 Sacherschließung
lokal Extracellular Matrix Proteins
lokal Cell Penetrating Peptides
lokal Cell Invasion
lokal Matrix Metalloproteinase (MMP)
lokal Fluorescence Resonance Energy Transfer (FRET)
lokal Imaging
lokal Enzyme Substrate Design
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/creator/TWV5ZXIsIEIuIFNpbmE=|http://orcid.org/0000-0001-6678-3165
1000 Label
1000 Förderer
  1. MolDiag-PaCa |
  2. EU |
1000 Fördernummer
  1. -
  2. LSH.2004-1.2.2.1
1000 Förderprogramm
  1. -
  2. Sixth Framework Programme Priority Grant
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer MolDiag-PaCa |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer EU |
    1000 Förderprogramm Sixth Framework Programme Priority Grant
    1000 Fördernummer LSH.2004-1.2.2.1
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6403557.rdf
1000 Erstellt am 2017-07-24T09:58:42.267+0200
1000 Erstellt von 25
1000 beschreibt frl:6403557
1000 Bearbeitet von 288
1000 Zuletzt bearbeitet 2022-08-18T07:55:24.114+0200
1000 Objekt bearb. Wed Mar 31 09:09:42 CEST 2021
1000 Vgl. frl:6403557
1000 Oai Id
  1. oai:frl.publisso.de:frl:6403557 |
1000 Sichtbarkeit Metadaten public
1000 Sichtbarkeit Daten public
1000 Gegenstand von

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