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

Research output: Journal article publicationJournal articleAcademic researchpeer-review

5 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
JournalSmall Methods
Volume8
Issue number11
DOIs
Publication statusPublished - 9 Apr 2024

Keywords

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

ASJC Scopus subject areas

  • General Chemistry
  • General Materials Science

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