HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Hybrid peptide dendrimers for imaging of chemokine receptor 4 (CXCR4) expression.

Abstract
The chemokine receptor 4 (CXCR4), which is overexpressed in many types of cancer, is an emerging target in the field of molecular imaging and therapeutics. The CXCR4 binding of several peptides, including the cyclic Ac-TZ14011, has already been validated. In this study mono-, di- and tetrameric Ac-TZ14011-containing dendrimers were prepared and functionalized with a multimodal (hybrid) label, consisting of a Cy5.5-like fluorophore and a DTPA chelate. Confocal microscopy revealed that all three dendrimers were membrane bound at 4 °C, consistent with CXCR4 binding in vitro. The unlabeled dimer and tetramer had a somewhat lower affinity for CXCR4 than the unlabeled monomer. However, when labeled with the multimodal label the CXCR4 affinity of the dimer and tetramer was considerably higher compared to that of the labeled monomer. On top of that, biodistribution studies revealed that the additional peptides in the dimer and tetramer reduced nonspecific muscle uptake. Thus, multimerization of the cyclic Ac-TZ14011 peptide reduces the negative influence of the multimodal label on the receptor affinity and the biodistribution.
AuthorsJoeri Kuil, Tessa Buckle, Joppe Oldenburg, Hushan Yuan, Alexander D Borowsky, Lee Josephson, Fijs W B van Leeuwen
JournalMolecular pharmaceutics (Mol Pharm) Vol. 8 Issue 6 Pg. 2444-53 (Dec 05 2011) ISSN: 1543-8392 [Electronic] United States
PMID22085282 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Dendrimers
  • Fluorescent Dyes
  • Peptides
  • Receptors, CXCR4
Topics
  • Cell Line, Tumor
  • Cell Survival
  • Dendrimers (chemistry, metabolism)
  • Diagnostic Imaging
  • Dimerization
  • Fluorescent Dyes (chemistry)
  • Gene Expression Profiling (methods)
  • Gene Expression Regulation
  • Humans
  • Microscopy, Confocal
  • Models, Molecular
  • Molecular Structure
  • Peptides (chemistry, metabolism)
  • Receptors, CXCR4 (chemistry, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: