Summary and Conclusion

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


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.


Aromatic Amino Acid Coiled Coil Protein Ligand Natural Amino Acid Antifungal Peptide 
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    Kohli RM, Walsh CT, Burkart MD et al (2002) Biomimetic synthesis and optimization of cyclic peptide antibiotics. Nature 418:658–661CrossRefGoogle Scholar
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    Srinivas N, Jetter P, Ueberbacher BJ et al (2010) Peptidominetic antibiotics target outer-membrane biogenesis in Pseudomonas aeruginose. Science 327:1010–1013CrossRefGoogle Scholar
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    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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