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2026

Journal Article

Progress and Challenges in the Biosynthesis and Chemical Synthesis of Lasso Peptides

Khatri, Bhavesh, Lay, Travis and Craik, David J. (2026). Progress and Challenges in the Biosynthesis and Chemical Synthesis of Lasso Peptides. Journal of the American Chemical Society, 148 (5) jacs.5c10593, 4777-4790. doi: 10.1021/jacs.5c10593

Progress and Challenges in the Biosynthesis and Chemical Synthesis of Lasso Peptides

2026

Journal Article

uPA-mediated remodeling of CCL21 gradients regulates lymphatic migration of dendritic cells

Collado-Diaz, Victor, Christakopoulou, Maria-Nefeli, Schineis, Philipp, Blatter, Katharina, Laubender, David, Trzebanski, Sébastien, Thoma, Marina, Gadient, Yves, Tatliadim, Hazal, Gkelis, Konstantinos, Friess, Mona C., Purvanov, Vladimir, Samson, Guerric P.B., Artinger, Marc, Bisoendial, Radjesh, Yepes, Manuel, de Veer, Simon J., Craik, David, Behrendt, Niels, Silina, Karina, Legler, Daniel F. and Halin, Cornelia (2026). uPA-mediated remodeling of CCL21 gradients regulates lymphatic migration of dendritic cells. Journal of Cell Biology, 225 (3) e202412190. doi: 10.1083/jcb.202412190

uPA-mediated remodeling of CCL21 gradients regulates lymphatic migration of dendritic cells

2026

Journal Article

Recent advances in structural and functional diversities of cancer lncRNA-encoded peptides: current opportunities and challenges for enhancing cancer diagnosis and treatment

Guo, Aimin, Wang, Shanshan, Huang, Linan, He, Yanping, Xi, Qing, Craik, David J. and Zhang, Jun (2026). Recent advances in structural and functional diversities of cancer lncRNA-encoded peptides: current opportunities and challenges for enhancing cancer diagnosis and treatment. Cancer Cell International, 26 (1) 67. doi: 10.1186/s12935-025-04158-2

Recent advances in structural and functional diversities of cancer lncRNA-encoded peptides: current opportunities and challenges for enhancing cancer diagnosis and treatment

2025

Journal Article

Deep learning-driven discovery and mechanism of action study of a minimalist conopeptide targeting α7 nicotinic acetylcholine receptor

Zhang, Jinghui, Yin, Zhengji, Li, Yue, Ge, Cheng, Zhang, Zixuan, Yuan, Pu, Jiang, Tao, Craik, David J., Zhao, Yan and Yu, Rilei (2025). Deep learning-driven discovery and mechanism of action study of a minimalist conopeptide targeting α7 nicotinic acetylcholine receptor. Acta Pharmaceutica Sinica B. doi: 10.1016/j.apsb.2025.12.035

Deep learning-driven discovery and mechanism of action study of a minimalist conopeptide targeting α7 nicotinic acetylcholine receptor

2025

Journal Article

Discovery of insecticidal cyclotides from the African plants Allexis batangae and Allexis obanensis

Khatibi, Negin, Eteme, Olivier Ndogo, Wang, Conan K., Gilding, Edward K., Zondegoumba, Ernestine Nkwengoua, Colgrave, Michelle L., Huang, Yen-Hua and Craik, David J. (2025). Discovery of insecticidal cyclotides from the African plants Allexis batangae and Allexis obanensis. Industrial Crops and Products, 237 122073, 1-9. doi: 10.1016/j.indcrop.2025.122073

Discovery of insecticidal cyclotides from the African plants Allexis batangae and Allexis obanensis

2025

Journal Article

Nickel-catalyzed cascade C-H alkynylation/hydroamination of free benzylamines for the synthesis of substituted 1H-isoindoles using a transient directing group strategy

Cai, Xinghao, Lu, Wei, Ma, Chen, Kang, Ying, Ren, Yuqiang, Meng, Xue, Craik, David J., Fan, Shiming, Chan, Lai Yue and Liu, Shouxin (2025). Nickel-catalyzed cascade C-H alkynylation/hydroamination of free benzylamines for the synthesis of substituted 1H-isoindoles using a transient directing group strategy. Chinese Journal of Chemistry, 43 (23) cjoc.70222, 3171-3177. doi: 10.1002/cjoc.70222

Nickel-catalyzed cascade C-H alkynylation/hydroamination of free benzylamines for the synthesis of substituted 1H-isoindoles using a transient directing group strategy

2025

Journal Article

Combining bioactive cell-penetrating peptides and vemurafenib to produce peptide-drug conjugates with activity against drug-resistant melanoma cells

Palombi, Isabella R., White, Andrew M., Koda, Yasuko, Craik, David J., Troeira Henriques, Sónia, Lawrence, Nicole and Malins, Lara R. (2025). Combining bioactive cell-penetrating peptides and vemurafenib to produce peptide-drug conjugates with activity against drug-resistant melanoma cells. Journal of Medicinal Chemistry, 68 (21), 23459-23471. doi: 10.1021/acs.jmedchem.5c02367

Combining bioactive cell-penetrating peptides and vemurafenib to produce peptide-drug conjugates with activity against drug-resistant melanoma cells

2025

Conference Publication

Recombinant production of an antimalarial peptide in Nicotiana benthamiana

Nguyen, Linh T.T., Harding, Maxim D., Healy, Wing L., Thanthrige, Nipuni P., Ninh, Thao T., Jackson, Mark A., Gilding, Edward K., Lawrence, Nicole and Craik, David (2025). Recombinant production of an antimalarial peptide in Nicotiana benthamiana. The 16th Australian Peptide Conference, Launceston, TAS, Australia, 12-17 October 2025.

Recombinant production of an antimalarial peptide in Nicotiana benthamiana

2025

Journal Article

Design of Bicyclic peptide tandems mimicking the homodimeric GDF15 protein to inhibit GDF15–GFRaL–RET complex cell signaling

Noisier, Anaïs F. M., Sandmark, Jenny, Edfeldt, Fredrik, Backmark, Anna, Broddefalk, Johan, Wandzik, Joanna, Jurva, Ulrik, Ek, Margareta, Johansson, Carina A., Barlind, Louise, Gunnarsson, Jenny, Bigalke, Janna M., Xue, Yafeng, Frolov, Andrey I., Kankkonen, Cecilia, Roth, Robert G., Fritsch, Maria, Watcham, Sophie, van Rietschoten, Katerine, Mudd, Gemma E., Harrison, Helen, Chen, Liuhong, Skynner, Michael J., Craik, David J., Chankeshwara, Sunay V. and Lemurell, Malin (2025). Design of Bicyclic peptide tandems mimicking the homodimeric GDF15 protein to inhibit GDF15–GFRaL–RET complex cell signaling. Journal of Medicinal Chemistry, 68 (20), 21441-21457. doi: 10.1021/acs.jmedchem.5c01378

Design of Bicyclic peptide tandems mimicking the homodimeric GDF15 protein to inhibit GDF15–GFRaL–RET complex cell signaling

2025

Journal Article

Where have you been? Backtracking microplastic to its source using the biomolecular composition of the ecocorona

Dawson, Amanda L., Bose, Utpal, Escobar-Correas, Sophia, Yap, Kuok, Craik, David J. and Pegg, Cassandra L. (2025). Where have you been? Backtracking microplastic to its source using the biomolecular composition of the ecocorona. Environmental Science and Technology, 59 (41), 22227-22238. doi: 10.1021/acs.est.5c09277

Where have you been? Backtracking microplastic to its source using the biomolecular composition of the ecocorona

2025

Journal Article

AEP-mediated backbone cyclization of cyclotides—a chemoenzymatic method for cyclotide production

Zhou, Yan, de Veer, Simon J., Durek, Thomas and Craik, David J. (2025). AEP-mediated backbone cyclization of cyclotides—a chemoenzymatic method for cyclotide production. Methods in Enzymology, 723, 71-90. doi: 10.1016/bs.mie.2025.09.001

AEP-mediated backbone cyclization of cyclotides—a chemoenzymatic method for cyclotide production

2025

Journal Article

Mixed-chirality prohibitin peptide: D-(RLARLAR)2 enhances stability and in vivo effects on obesity

Chan, Lai Yue, Weger, Benjamin D., Weger, Meltem, Du, Junqiao, Lawrence, Nicole, Cardoso, Marlon H., de Rezende, Samilla B., Muller, Jéssica A.I., Yap, Kuok, Tse, Brian W−C., Sokolowski, Kamil A., Sullivan, Robert K.P., Gunter, Jennifer, Franco, Octávio L., Gachon, Frédéric and Craik, David J. (2025). Mixed-chirality prohibitin peptide: D-(RLARLAR)2 enhances stability and in vivo effects on obesity. Journal of the American Chemical Society, 147 (28), 24628-24642. doi: 10.1021/jacs.5c05536

Mixed-chirality prohibitin peptide: D-(RLARLAR)2 enhances stability and in vivo effects on obesity

2025

Journal Article

Asparaginyl ligases with engineered substrate specificity for controlled, sequential transpeptidation reactions

Zhou, Yan, de Veer, Simon J., Tyler, Tristan J., Chen, Yufei, Durek, Thomas, Craik, David J. and Rehm, Fabian B. H. (2025). Asparaginyl ligases with engineered substrate specificity for controlled, sequential transpeptidation reactions. Journal of the American Chemical Society, 147 (25), 21824-21831. doi: 10.1021/jacs.5c04693

Asparaginyl ligases with engineered substrate specificity for controlled, sequential transpeptidation reactions

2025

Journal Article

High-throughput enrichment of functional disulfide-rich peptides by droplet microfluidics

Xie, Jing, Yap, Kuok, de Veer, Simon J., Edwardraja, Selvakumar, Durek, Thomas, Trau, Matt, Craik, David J. and Wang, Conan K. (2025). High-throughput enrichment of functional disulfide-rich peptides by droplet microfluidics. Lab on a Chip, 25 (14), 3525-3536. doi: 10.1039/d5lc00261c

High-throughput enrichment of functional disulfide-rich peptides by droplet microfluidics

2025

Journal Article

Exploring use of a protein cage system for producing bioactive peptides in Escherichia coli

Harding, Maxim D., Jackson, Mark A., Gilding, Edward K., Yap, Kuok, Craik, David J., Sainsbury, Frank and Lawrence, Nicole (2025). Exploring use of a protein cage system for producing bioactive peptides in Escherichia coli. Microbial Biotechnology, 18 (6) e70158, 1-14. doi: 10.1111/1751-7915.70158

Exploring use of a protein cage system for producing bioactive peptides in Escherichia coli

2025

Journal Article

Cyclization of the analgesic α‐Conotoxin Vc1.1 with a non‐natural linker: effects on structure, stability, and bioactivity

Zhang, Yuhui, Tae, Han Shen, Adams, David J., Durek, Thomas and Craik, David J. (2025). Cyclization of the analgesic α‐Conotoxin Vc1.1 with a non‐natural linker: effects on structure, stability, and bioactivity. Journal of Peptide Science, 31 (6) e70017, 1-10. doi: 10.1002/psc.70017

Cyclization of the analgesic α‐Conotoxin Vc1.1 with a non‐natural linker: effects on structure, stability, and bioactivity

2025

Journal Article

An orthogonal protection strategy for the synthesis of conotoxins containing three disulfide bonds

Zhang, Hengyu, Chan, Lai Yue, Zhang, Huanhuan, Jiang, Tao, Craik, David J., Cai, Wenqing and Yu, Rilei (2025). An orthogonal protection strategy for the synthesis of conotoxins containing three disulfide bonds. Marine Drugs, 23 (4) 168, 1-11. doi: 10.3390/md23040168

An orthogonal protection strategy for the synthesis of conotoxins containing three disulfide bonds

2025

Journal Article

Anticoagulation during Extracorporeal Membrane Oxygenation (ECMO): A Selective Inhibitor of Activated Factor XII Compared to Heparin in an Ex Vivo Model

Gandini, Lucia, de Veer, Simon J., Chan, Chris H. H., Passmore, Margaret R., Liu, Keibun, Lundon, Brooke, Rachakonda, Reema, White, Nicole, Rhodes, Madeleine, Shanahan, Emma, Yap, Kuok, See Hoe, Louise E., Semenzin, Clayton, Li Bassi, Gianluigi, Fraser, John F., Craik, David J. and Suen, Jacky Y. (2025). Anticoagulation during Extracorporeal Membrane Oxygenation (ECMO): A Selective Inhibitor of Activated Factor XII Compared to Heparin in an Ex Vivo Model. ACS Pharmacology & Translational Science, 8 (5), 1260-1269. doi: 10.1021/acsptsci.4c00352

Anticoagulation during Extracorporeal Membrane Oxygenation (ECMO): A Selective Inhibitor of Activated Factor XII Compared to Heparin in an Ex Vivo Model

2025

Journal Article

Selective inhibition of Rat α7 nicotinic acetylcholine receptors by LvID, a newly characterized α4/7-conotoxin from Conus lividus

Guo, Man, Zhu, Xiaopeng, Ma, Tao, Xu, Chenxing, Zhangsun, Dongting, Yu, Jinpeng, Kaas, Quentin, Harvey, Peta J., McIntosh, J. Michael, Craik, David J. and Luo, Sulan (2025). Selective inhibition of Rat α7 nicotinic acetylcholine receptors by LvID, a newly characterized α4/7-conotoxin from Conus lividus. Journal of Medicinal Chemistry, 68 (8), 8163-8173. doi: 10.1021/acs.jmedchem.4c02810

Selective inhibition of Rat α7 nicotinic acetylcholine receptors by LvID, a newly characterized α4/7-conotoxin from Conus lividus

2025

Journal Article

Cell-penetrating cyclic and disulfide-rich peptides are privileged molecular scaffolds for intracellular targeting

Troeira Henriques, Sónia, Lawrence, Nicole, Kan, Meng-Wei, Malins, Lara R. and Craik, David J. (2025). Cell-penetrating cyclic and disulfide-rich peptides are privileged molecular scaffolds for intracellular targeting. Biochemistry, 64 (7), 1437-1449. doi: 10.1021/acs.biochem.4c00845

Cell-penetrating cyclic and disulfide-rich peptides are privileged molecular scaffolds for intracellular targeting