In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin Substrate

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Hai Yu Hu
  • Divya Vats
  • Matej Vizovisek
  • Lovro Kramer
  • Catherine Germanier
  • K. Ulrich Wendt
  • Markus Rudin
  • Boris Turk
  • Oliver Plettenburg
  • Carsten Schultz

Externe Organisationen

  • Universität Zürich (UZH)
  • Institut "Jožef Stefan" (IJS)
  • Centre of Excellence for Integrated Approaches in Chemistry and Biology of Proteins (CIPKeBiP)
  • University of Ljubljana
  • Jožef Stefan International Postgraduate School (IPS)
  • European Molecular Biology Laboratory (EMBL)
  • Sanofi-Aventis Deutschland GmbH
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)7669-7673
Seitenumfang5
FachzeitschriftAngewandte Chemie - International Edition
Jahrgang53
Ausgabenummer29
Frühes Online-Datum30 Mai 2014
PublikationsstatusVeröffentlicht - 14 Juli 2014
Extern publiziertJa

Abstract

The synthesis and evaluation of two cathepsin S-specific probes is described. For long-term retention of the probe at the target site and a high signal-to-noise ratio, we introduced a lipidation approach via the simple attachment of palmitoic acid to the reporter. After cathepsin S-specific cleavage in cultured cells and in a grafted tumor mouse model, fluorescence increased owing to dequenching and we observed an intracellular accumulation of the fluorescence in the target tissue. The lipidated probe provided a prolonged and strongly fluorescent signal in tumors when compared to the very similar non-lipidated probe, demonstrating that non-invasive tumor identification is feasable. The homing principle by probe lipidation might also work for selective administration of cytotoxic compounds to specifically reduce tumor mass.

ASJC Scopus Sachgebiete

Zitieren

In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin Substrate. / Hu, Hai Yu; Vats, Divya; Vizovisek, Matej et al.
in: Angewandte Chemie - International Edition, Jahrgang 53, Nr. 29, 14.07.2014, S. 7669-7673.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Hu, HY, Vats, D, Vizovisek, M, Kramer, L, Germanier, C, Wendt, KU, Rudin, M, Turk, B, Plettenburg, O & Schultz, C 2014, 'In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin Substrate', Angewandte Chemie - International Edition, Jg. 53, Nr. 29, S. 7669-7673. https://doi.org/10.1002/anie.201310979
Hu, H. Y., Vats, D., Vizovisek, M., Kramer, L., Germanier, C., Wendt, K. U., Rudin, M., Turk, B., Plettenburg, O., & Schultz, C. (2014). In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin Substrate. Angewandte Chemie - International Edition, 53(29), 7669-7673. https://doi.org/10.1002/anie.201310979
Hu HY, Vats D, Vizovisek M, Kramer L, Germanier C, Wendt KU et al. In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin Substrate. Angewandte Chemie - International Edition. 2014 Jul 14;53(29):7669-7673. Epub 2014 Mai 30. doi: 10.1002/anie.201310979
Hu, Hai Yu ; Vats, Divya ; Vizovisek, Matej et al. / In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin Substrate. in: Angewandte Chemie - International Edition. 2014 ; Jahrgang 53, Nr. 29. S. 7669-7673.
Download
@article{fab14aa3c00a4796b51f35c1cdcd415a,
title = "In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin Substrate",
abstract = "The synthesis and evaluation of two cathepsin S-specific probes is described. For long-term retention of the probe at the target site and a high signal-to-noise ratio, we introduced a lipidation approach via the simple attachment of palmitoic acid to the reporter. After cathepsin S-specific cleavage in cultured cells and in a grafted tumor mouse model, fluorescence increased owing to dequenching and we observed an intracellular accumulation of the fluorescence in the target tissue. The lipidated probe provided a prolonged and strongly fluorescent signal in tumors when compared to the very similar non-lipidated probe, demonstrating that non-invasive tumor identification is feasable. The homing principle by probe lipidation might also work for selective administration of cytotoxic compounds to specifically reduce tumor mass.",
keywords = "fluorescence probes, FRET, homing, lipidation, tumor diagnosis",
author = "Hu, {Hai Yu} and Divya Vats and Matej Vizovisek and Lovro Kramer and Catherine Germanier and Wendt, {K. Ulrich} and Markus Rudin and Boris Turk and Oliver Plettenburg and Carsten Schultz",
year = "2014",
month = jul,
day = "14",
doi = "10.1002/anie.201310979",
language = "English",
volume = "53",
pages = "7669--7673",
journal = "Angewandte Chemie - International Edition",
issn = "1433-7851",
publisher = "John Wiley and Sons Ltd",
number = "29",

}

Download

TY - JOUR

T1 - In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin Substrate

AU - Hu, Hai Yu

AU - Vats, Divya

AU - Vizovisek, Matej

AU - Kramer, Lovro

AU - Germanier, Catherine

AU - Wendt, K. Ulrich

AU - Rudin, Markus

AU - Turk, Boris

AU - Plettenburg, Oliver

AU - Schultz, Carsten

PY - 2014/7/14

Y1 - 2014/7/14

N2 - The synthesis and evaluation of two cathepsin S-specific probes is described. For long-term retention of the probe at the target site and a high signal-to-noise ratio, we introduced a lipidation approach via the simple attachment of palmitoic acid to the reporter. After cathepsin S-specific cleavage in cultured cells and in a grafted tumor mouse model, fluorescence increased owing to dequenching and we observed an intracellular accumulation of the fluorescence in the target tissue. The lipidated probe provided a prolonged and strongly fluorescent signal in tumors when compared to the very similar non-lipidated probe, demonstrating that non-invasive tumor identification is feasable. The homing principle by probe lipidation might also work for selective administration of cytotoxic compounds to specifically reduce tumor mass.

AB - The synthesis and evaluation of two cathepsin S-specific probes is described. For long-term retention of the probe at the target site and a high signal-to-noise ratio, we introduced a lipidation approach via the simple attachment of palmitoic acid to the reporter. After cathepsin S-specific cleavage in cultured cells and in a grafted tumor mouse model, fluorescence increased owing to dequenching and we observed an intracellular accumulation of the fluorescence in the target tissue. The lipidated probe provided a prolonged and strongly fluorescent signal in tumors when compared to the very similar non-lipidated probe, demonstrating that non-invasive tumor identification is feasable. The homing principle by probe lipidation might also work for selective administration of cytotoxic compounds to specifically reduce tumor mass.

KW - fluorescence probes

KW - FRET

KW - homing

KW - lipidation

KW - tumor diagnosis

UR - http://www.scopus.com/inward/record.url?scp=84904438282&partnerID=8YFLogxK

U2 - 10.1002/anie.201310979

DO - 10.1002/anie.201310979

M3 - Article

C2 - 24888522

AN - SCOPUS:84904438282

VL - 53

SP - 7669

EP - 7673

JO - Angewandte Chemie - International Edition

JF - Angewandte Chemie - International Edition

SN - 1433-7851

IS - 29

ER -

Von denselben Autoren