An improved fluorescent substrate for assaying soluble and membrane-associated ADAM family member activities

  • Marcia L. Moss
  • , Dmitriy Minond
  • , Toshie Yoneyama
  • , Hinrich P. Hansen
  • , Nikola Vujanovic
  • , Fred H. Rasmussen

Research output: Contribution to journalArticlepeer-review

Abstract

A fluorescent resonance energy transfer substrate with improved sensitivity for ADAM17, -10, and -9 (where ADAM represents a disintegrin and metalloproteinase) has been designed. The new substrate, Dabcyl-Pro-Arg-Ala-Ala-Ala-Homophe-Thr-Ser-Pro-Lys(FAM)-NH2, has specificity constants of 6.3 (±0.3) × 104 M-1 s-1 and 2.4 (±0.3) × 103 M-1 s-1 for ADAM17 and ADAM10, respectively. The substrate is more sensitive than widely used peptides based on the precursor tumor necrosis factor-alpha (TNF-alpha) cleavage site, PEPDAB010 or Dabcyl-Ser-Pro-Leu-Ala-Gln-Ala-Val-Arg-Ser-Ser-Lys(FAM)-NH2 and Mca-Pro-Leu-Ala-Gln-Ala-Val-Dpa-Arg-Ser-Ser-Arg-NH2. ADAM9 also processes the new peptide more than 18-fold better than the TNF-alpha-based substrates. The new substrate has a unique selectivity profile because it is processed less efficiently by ADAM8 and MMP1, -2, -3, -8, -9, -12, and -14. This substrate provides a unique tool in which to assess ADAM17, -10, and -9 activities.

Original languageEnglish
Pages (from-to)13-17
Number of pages5
JournalAnalytical Biochemistry
Volume507
DOIs
StatePublished - Aug 15 2016
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2016 Elsevier Inc.

ASJC Scopus Subject Areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

Keywords

  • ADAM10
  • ADAM17
  • ADAM9
  • Assay
  • Extracellular vesicles
  • Fluorescent substrate

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