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Summary and Conclusion

  • Jianpeng WangEmail author
Chapter
Part of the Springer Theses book series (Springer Theses)

Abstract

During my graduate studies, I have been involved in three different but related areas: (1) structure–activity relationship of antimicrobial peptide defensin, (2) structure-guided design of protein ligands for quantum dots, and (3) structure-guided design of new bioconjugation reaction for cell imaging.

Keywords

Aromatic Amino Acid Coiled Coil Protein Ligand Natural Amino Acid Antifungal Peptide 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. 1.
    Kohli RM, Walsh CT, Burkart MD et al (2002) Biomimetic synthesis and optimization of cyclic peptide antibiotics. Nature 418:658–661CrossRefGoogle Scholar
  2. 2.
    Srinivas N, Jetter P, Ueberbacher BJ et al (2010) Peptidominetic antibiotics target outer-membrane biogenesis in Pseudomonas aeruginose. Science 327:1010–1013CrossRefGoogle Scholar
  3. 3.
    Chang CH, Rossi EA, Goldenberg DM et al (2007) The dock and lock method: a novel platform technology for building multivalent, multifunctional structures of defined composition with retained bioactivity. Clin Cancer Res 13:5586–5591CrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2016

Authors and Affiliations

  1. 1.Department of ChemistryThe Chinese University of Hong KongHong KongChina

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