4.4 Review

Cyclic Peptides as Therapeutic Agents and Biochemical Tools

Journal

BIOMOLECULES & THERAPEUTICS
Volume 20, Issue 1, Pages 19-26

Publisher

KOREAN SOC APPLIED PHARMACOLOGY
DOI: 10.4062/biomolther.2012.20.1.019

Keywords

Cyclic peptides; Split-and-pool synthesis; On-bead screening; Drug lead

Funding

  1. National Research Foundation of Korea (NRF)
  2. Korea government (MEST) [2010-0003008]
  3. Catholic University of Daegu
  4. National Research Foundation of Korea [2010-0003008] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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There are many cyclic peptides with diverse biological activities, such as antibacterial activity, immunosuppressive activity, and anti-tumor activity, and so on. Encouraged by natural cyclic peptides with biological activity, efforts have been made to develop cyclic peptides with both genetic and synthetic methods. The genetic methods include phage display, intein-based cyclic peptides, and mRNA display. The synthetic methods involve individual synthesis, parallel synthesis, as well as split-and-pool synthesis. Recent development of cyclic peptide library based on split-and-pool synthesis allows on-bead screening, in-solution screening, and nnicroarray screening of cyclic peptides for biological activity. Cyclic peptides will be useful as receptor agonist/antagonist, RNA binding molecule, enzyme inhibitor and so on, and more cyclic peptides will emerge as therapeutic agents and biochemical tools.

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