Kaycie M. Deyle

发表

Cyclic peptide therapeutics: past, present and future.

C. Heinis, Christian Heinis, K. Deyle, 2017, Current opinion in chemical biology.

Development of Protein-Catalyzed Capture (PCC) Agents with Application to the Specific Targeting of the E17K Point Mutation of Akt1

Kaycie Marie Deyle, Kaycie M. Deyle, 2014 .

Cyclization of peptides with two chemical bridges affords large scaffold diversities

X. Kong, C. Heinis, K. Deyle, 2018, Nature Chemistry.

Correction to A Chemically Synthesized Capture Agent Enables the Selective, Sensitive, and Robust Electrochemical Detection of Anthrax Protective Antigen.

Amethist S. Finch, Matthew B. Coppock, Dimitra N. Stratis-Cullum, 2018, ACS nano.

Epitope targeting of tertiary protein structure enables target-guided synthesis of a potent in-cell inhibitor of botulinum neurotoxin.

J. Heath, Heather D Agnew, B. Lai, 2015, Angewandte Chemie.

De novo development of proteolytically resistant therapeutic peptides for oral administration

F. Pojer, L. Abriata, X. Kong, 2020, Nature Biomedical Engineering.

Acylated heptapeptide binds albumin with high affinity and application as tag furnishes long-acting peptides

C. Heinis, K. Deyle, Alessandro Zorzi, 2017, Nature Communications.

Phage Selection of Cyclic Peptides for Application in Research and Drug Development.

X. Kong, C. Heinis, Kaycie M. Deyle, 2017, Accounts of chemical research.

A Cocktail of Thermally Stable, Chemically Synthesized Capture Agents for the Efficient Detection of Anti-Gp41 Antibodies from Human Sera

Jocelyn T. Kim, J. Heath, B. Lai, 2013, PloS one.

De novo development of proteolytically resistant therapeutic peptides for oral administration

F. Pojer, L. Abriata, X. Kong, 2020, Nature Biomedical Engineering.

De novo evolution of target-specific peptides that survive oral administration

F. Pojer, L. Abriata, X. Kong, 2020 .

A chemically synthesized capture agent enables the selective, sensitive, and robust electrochemical detection of anthrax protective antigen.

Amethist S. Finch, Matthew B. Coppock, Dimitra N. Stratis-Cullum, 2013, ACS nano.

Iterative in situ click chemistry assembles a branched capture agent and allosteric inhibitor for Akt1.

Su Seong Lee, K. Sharpless, Jaehong Lim, 2011, Journal of the American Chemical Society.

Engineered peptide macrocycles can inhibit matrix metalloproteinases with high selectivity.

X. Kong, C. Heinis, M. Sabisz, 2019, Angewandte Chemie.

Cyclic peptide FXII inhibitor provides safe anticoagulation in a thrombosis model and in artificial lungs

R. Rieben, C. Lamers, X. Kong, 2020, Nature Communications.

Thiol-to-amine cyclization reaction enables screening of large libraries of macrocyclic compounds and the generation of sub-kilodalton ligands

M. G. Kumar, Manh V. Pham, G. Turcatti, 2019, Science Advances.

Protein-targeting strategy used to develop a selective inhibitor of the E17K point mutation in the PH Domain of Akt1

J. Heath, B. Lai, K. Deyle, 2015, Nature chemistry.

A chemical epitope-targeting strategy for protein capture agents: the serine 474 epitope of the kinase Akt2.

J. Heath, K. Deyle, S. Millward, 2013, Angewandte Chemie.