Facile Peptide Macrocyclization and Multifunctionalization via Cyclen Installation

Tsz Lam Cheung, Leo K.B. Tam, Wing Sze Tam, Leilei Zhang, Hei Yui Kai, Waygen Thor, Yue Wu, Pak Lun Lam, Yik Hoi Yeung, Chen Xie, Ho Fai Chau, Wai Sum Lo, Tao Zhang*, Ka Leung Wong*

*Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

3 Citations (Scopus)

Abstract

Cyclen-peptide bioconjugates are usually prepared in multiple steps that require individual preparation and purification of the cyclic peptide and hydrophilic cyclen derivatives. An efficient strategy is discovered for peptide cyclization and functionalization toward lanthanide probe via three components intermolecular crosslinking on solid-phase peptide synthesis with high conversion yield. Multifunctionality can be conferred by introducing different modular parts or/and metal ions on the cyclen-embedded cyclopeptide. As a proof-of-concept, a luminescent Eu3+ complex and a Gd3+-based contrasting agent for in vitro optical imaging and in vivo magnetic resonance imaging, respectively, are demonstrated through utilizing this preparation of cyclen-embedded cyclic arginylglycylaspartic acid (RGD) peptide.

Original languageEnglish
Article number2400006
Number of pages7
JournalSmall Methods
Volume8
Issue number11
Early online date9 Apr 2024
DOIs
Publication statusPublished - 20 Nov 2024

Scopus Subject Areas

  • General Chemistry
  • General Materials Science

User-Defined Keywords

  • cyclen-peptide conjugates
  • lanthanides
  • luminescence
  • solid phase peptide synthesis
  • αβ integrin

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