About | XPad: XJTLU Peptide and Drug Research Group

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Led by Dr. Shining Loo (Wisdom Lake Academy of Pharmacy) and Dr. Antony Kam (Department of Biological Sciences) at Xi'an JiaoTong Liverpool University), XPad (XJTLU Peptide and Drug) is a collaborative research group at the forefront of peptide-based technologies. We leverage our expertise in molecular pharmacology, synthetic biology, and chemical biology to develop innovative solutions.

 

 

Welcome to XPad: Where Peptides Meet Healthcare Innovation!

 

Led by Dr. Antony Kam (Department of Biosciences and Bioinformatics) and Dr. Shining Loo (Wisdom Lake Academy of Pharmacy) at Xi'an JiaoTong Liverpool University, XPad (XJTLU Peptide and Drug) is a collaborative research group at the forefront of peptide-based technologies. We leverage our expertise in molecular pharmacology, synthetic biology, and chemical biology to develop innovative solutions for:

 

  • Therapeutics: Designing next-generation drugs with targeted precision to combat various diseases.

  • Diagnostics: Creating highly accurate and personalized medical tests for early disease detection and personalized treatment.

  • Biomaterials: Engineering advanced materials for tissue regeneration and repair, promoting healing and improving lives.

  • Drug Delivery Systems: Revolutionizing how therapeutics are delivered safely and effectively, maximizing their impact.

What we do?

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XPad Technology Platform

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Our Heritage: From a Nobel Prize to Next-Generation Science

Our Heritage: From a Nobel Prize to Next-Generation Science

The scientific foundation of XPad is rooted in a distinguished history of excellence in peptide chemistry. Our lineage connects directly to Nobel Laureate Dr. Robert Bruce Merrifield at Rockefeller University, whose invention of solid-phase peptide synthesis revolutionized the field.

 

The Foundational Link: Professor James P. Tam

This prestigious connection comes through our mentor, the world-renowned chemist Professor James P. Tam. As a member and collaborator of Dr. Merrifield's group, Professor Tam collaborated with him for nearly 16 years, a period that included Dr. Merrifield's 1984 Nobel Prize in Chemistry. This formative experience ignited Professor Tam's own passion and shaped his pivotal contributions to the field.

A leading figure in his own right, Professor Tam's pioneering work in peptide dendrimers, chemoselective ligation methods, and the discovery of ultra-stable peptides has had a profound impact on chemical biology and drug discovery. His excellence is recognized by the highest honors in the field, including the Bruce Merrifield Award and the Ralph Hirschman Award.

 

The Next Chapter: The XPad Lab

As founders of XPad, we honed our expertise under Professor Tam's mentorship at Nanyang Technological University. Today, we carry that legacy forward. Our work stands at the intersection of groundbreaking history and modern application, driven by a passion for discovery passed down through generations of leading scientists.

 

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Professor James P. Tam is a distinguished Fellow of the Singapore National Academy of Science and a pioneering leader in chemical biology and drug discovery. Since 2001, he has held the prestigious Lee Wee Nam Professorship at the School of Biological Sciences, Nanyang Technological University (NTU), Singapore, where he leads the Herbalomics and Drug Discovery Laboratory. Since 2008, he has also served as Director of the Synzymes and Natural Products Center (SYNC). As a visionary academic leader, Professor Tam founded School of Biological Sciences, the Biological Research Center and the innovative Double-Degree Program in Biomedical Science and Chinese Medicine at NTU, bridging traditional and modern approaches to therapeutic discovery.

Professor Tam earned his Ph.D. from the University of Wisconsin, Madison, and subsequently held professorial appointments at three world-renowned institutions: The Rockefeller University, Vanderbilt University, and The Scripps Research Institute. His distinguished career trajectory reflects his exceptional contributions to the field and his recognition by leading academic institutions.

A defining moment in Professor Tam's career began in 1976 when he joined Bruce Merrifield's laboratory at The Rockefeller University. This collaboration, spanning nearly 16 years, coincided with Merrifield's groundbreaking work in solid-phase protein synthesis—research that would earn Merrifield the Nobel Prize in Chemistry in 1984. During this pivotal period, Professor Tam developed his passion for peptide synthesis and contributed significantly to advancing solid-phase synthesis techniques, laying the foundation for his own pioneering research contributions.

Professor Tam has established himself as a world leader in therapeutics, with particular expertise in the discovery and development of orally active biologics, immunologics, and anti-infectives. His research encompasses advanced peptide and protein chemistry, including selective chemoenzymatic ligation, as well as the synthesis and oxidative folding of cysteine-rich peptides. His innovative approach extends to developing therapeutic solutions derived from natural products, representing a unique integration of traditional and modern drug discovery methods.

His research portfolio encompasses several groundbreaking discoveries, including the invention of peptide dendrimers as synthetic vaccines and protein quaternary structure mimetics. He has pioneered chemoselective peptide ligation methods and discovered novel peptide ligases. Additionally, his work has led to the discovery of ultra-stable cysteine-rich peptides from medicinal plants with significant therapeutic potential, opening new avenues for drug development.

Professor Tam's research excellence is reflected in his impressive publication record of over 330 papers, with an H-index of 97 and more than 31,600 Google Scholar citations. His work has produced seminal publications that have profoundly impacted chemical biology and drug discovery. His exceptional contributions have earned him numerous prestigious international awards, including the Bruce Merrifield Award from the American Peptide Society, the Ralph Hirschman Award from the American Chemical Society, the Akabori Memorial Award from the Japanese Peptide Society, the Josef Rudinger Memorial Lecture Award from the European Peptide Society, and the Murray Goodman Scientific Excellence & Mentorship Award from the American Peptide Society.

Professor Tam's career exemplifies the intersection of fundamental scientific discovery and practical therapeutic innovation, making him one of the most influential figures in modern peptide science and drug discovery. His multifaceted contributions span from basic research in chemical synthesis to applied therapeutics, establishing him as a transformative leader in the field who continues to shape the future of drug discovery and development.

Alumni

Master students:

Ms Yueyi Jia [BIO]

 

FYP students:

Ms Yudi Liu, Ms Yue Yao, Mr Junqiang Niu, Mr Jiajun Lu, Mr Rui Hong

 

Summer Undergraduate Research Fellowship (SURF) students:

  • Group 2023-0071 [BIO] - Outstanding poster

            Mr Junqiang Niu, Ms Yifei Wang, Ms Yige Xu, Ms Yudi Liu, Ms Yue Yao, Mr Zhouxiang Gu

  • Group 2023-0072 [AoP] - Outstanding poster

           Mr Jingyu Jiang, Ms Shiqi Wang, Ms Ye Liu, Ms Yijia Yao, Ms Yunshan Tong, Ms Ziyu Yuan

  • Group 2024-0119 [BIO] - excellent poster

           Mr Haoyu Feng, Ms Yining Ren, Ms Shuqin Shen, Mr Linpei Xu, Ms Feiyang Xue, Mr Mingbai Zeng

  • Group 2024-0120 [AoP] - excellent poster

           Ms Yirong Bai, Ms Weijia Cai, Mr Wenbo Chen, Mr An Jiang, Ms Yiran Sun, Ms Songnan Wang

 

Overseas exchange students:

Mr Joe Munro (University of Liverpool, Department of Chemistry)

Ms Gui Jen Koh (Taylor's University)

Laboratory facilities and equipments

XPad Lab @ SB356 [BIO]

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Main benches

 

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Peptide synthesis 

 

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Cell culture 

 

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Solid Phase Extraction

 

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PCR/Bacteria hood

 

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Electrospinning and nanoparticle production device

 

XPad Lab @ P020 [AoP]

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Main benches

 

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In-house protein purification system

 

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In-house 5L bioreactor

 

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Temperature controlled bacterial expression

 

Core facilities @ BIO

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Flow cytometer

 

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Zeiss confocal microscope

 

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Oxford nanopore sequencing

 

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Microplate reader

 

Core facilities @ AoP

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Akta FPLC

 

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Agilent prep-HPLC

 

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Agilent Lc-qToF-MS/MS

 

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Thermofisher orbitrap ELITE

 

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Olympus spinning disk confocal microscope

 

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Peptide synthesizer

 

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Flash chromatography

 

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DLS

 

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HPLC

 

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Cytation 5

 

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Freeze drier

 

Core facilities @ CHEM

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Prep-HPLC

 

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HPLC

Created: 19 January 2024

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Group category: Research

  • 14 Members
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Group administrators: Antony Kam's profile picture Antony Kam Shining Loo's profile picture Shining Loo

Greetings

The XPad research group welcomes interested academic and industrial collaborations as well as students to join our group. Interested parties can contact via e-mail: shining.loo@xjtlu.edu.cn or antony.kam@xjtlu.edu.cn

 

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Current members

Principal investigators:

Dr Shining Loo [AoP]

https://scholar.xjtlu.edu.cn/en/persons/ShiningLoo

Dr Antony Kam [BIO]

https://scholar.xjtlu.edu.cn/en/persons/AntonyKam

 

Research technicians:

Ms Chunyue Du [BIO]

 

PhD students:

Mr Hongfei Wang [AOP]

 

Master students:

Ms Xiaoyun Liu [BIO]

Ms Yuxian Wang [BIO-JITRI]

Ms Xinge Li [AoP]

Ms Yani Gu [AoP]

Mr Shuhan Zhao [AoP]

Mr Liqiang Wei [AoP]

Mr Huaimu Jiang [AoP]

Mr Junqiang Niu [BIO]

Mr Jiajun Lu [BIO]

Ms Xiru Zhao [BIO]

Mr Qi Sun [AoP]

Ms Tianyun Xu [AoP]

Ms Xiaoyi Meng [AoP]

Ms Xinyang He [AoP]

Ms Yiran Wang [AoP]

Ms Yuewen Li [AoP]

 

Final year project students:

Mr Linpei Xu [BIO]

Ms Feiyang Xue [BIO]

Mr An Jiang [AOP]

Mr Lai Jiang [AOP]

Ms Yirong Bai [AOP]

Ms Jingyi Liu [AOP]

Ms Weijia Cai [AOP]

Mr Wenbo Chen [AOP]

Ms Mingyi Geng [AOP]

Mr Yiran Sun [AOP]

 

SURF students:

Mr Tianyi Ji (BIO)
Ms Songnan Wang (BIO)
Ms Yueyi Jiang (BIO)
Ms Wantong Li (BIO)
Ms Jingyi Cao (BIO)
Mr Pengyu Zhang (BIO)

Mr Jiang An (AOP)
Ms Jingyi Liu (AOP)
Mr Lai Jiang (AOP)
Ms Xumeng He (AOP)
Ms Mengyi Geng (AOP)
Ms Zimo Bai (AOP)

Chow Mun Hoe (Taylor's University)

Research publications RSS

Research publications

Proteomics in Systems Biology: Methods and Protocols

Skin-penetrating peptides (SKPs): Enhancing skin permeation for transdermal delivery of pharmaceuticals and cosmetic compounds

Muhammad, A.M., Ismail, A., Chong, P.P., Yap, W.H., Muhamad, A., Alitheen, N.B., Kam, A., Loo, S. and Lee, K.W., 2025. Skin-penetrating peptides (SKPs): Enhancing skin permeation for transdermal delivery of pharmaceuticals and cosmetic compounds. International Journal of Pharmaceutics, p.125339.

Cell-Permeable Microprotein from Panax Ginseng Protects Against Doxorubicin-Induced Oxidative Stress and Cardiotoxicity

Dutta, B., Loo, S., Kam, A., Wang, X., Wei, N., Luo, K.Q., Liu, C.F. and Tam, J.P., 2025. Cell-Permeable Microprotein from Panax Ginseng Protects Against Doxorubicin-Induced Oxidative Stress and Cardiotoxicity. Antioxidants, 14(4), p.493.

Ultrafast Biomimetic Oxidative Folding of Cysteine-rich Peptides and Microproteins in Organic Solvents,

Kam, A., Loo, S., Qiu, Y., Liu, C.F. and Tam, J.P., Ultrafast Biomimetic Oxidative Folding of Cysteine-rich Peptides and Microproteins in Organic Solvents, Angewandte Chemie. (Accepted)

https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.202317789

Ginsentide-like coffeetides isolated from coffee waste are cell-penetrating and metal-binding microproteins

Tam, J.P., Huang, J., Loo, S., Li, Y. and Kam, A., 2023. Ginsentide-like coffeetides isolated from coffee waste are cell-penetrating and metal-binding microproteins. Molecules28(18), p.6556.

https://www.mdpi.com/1420-3049/28/18/6556

Editorial on Special Issue “Natural Products for Drug Discovery and Development”

Kam, A., Loo, S. and Lee, S.M.Y., 2023. Editorial on Special Issue “Natural Products for Drug Discovery and Development”. Processes11(6), p.1784.

https://www.mdpi.com/2227-9717/11/6/1784

Ginsentide TP1 Protects Hypoxia-Induced Dysfunction and ER Stress-Linked Apoptosis

Dutta, B., Loo, S., Kam, A., Sze, S.K. and Tam, J.P., 2023. Ginsentide TP1 Protects Hypoxia-Induced Dysfunction and ER Stress-Linked Apoptosis. Cells12(10), p.1401.

https://www.mdpi.com/2073-4409/12/10/1401

Plant-derived cell-penetrating microprotein α-astratide aM1 targets Akt signaling and alleviates insulin resistance.

Dutta, B., Loo, S., Kam, A. and Tam, J.P., 2023. Plant-derived cell-penetrating microprotein α-astratide aM1 targets Akt signaling and alleviates insulin resistance. Cellular and Molecular Life Sciences80(10), p.293.

https://link.springer.com/article/10.1007/s00018-023-04937-y

Broad-spectrum ginsentides are principal bioactives in unraveling the cure-all effects of ginseng

Loo, S., Kam, A., Dutta, B., Zhang, X., Feng, N., Sze, S.K., Liu, C.F., Wang, X. and Tam, J.P., 2024. Broad-spectrum ginsentides are principal bioactives in unraveling the cure-all effects of ginseng. Acta Pharmaceutica Sinica B14(2), pp.653-666.

https://www.sciencedirect.com/science/article/pii/S2211383523004227 

9 entries
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Patents/Patent applications RSS

Patents/Patent applications

Cysteine-rich polypeptides and conjugates and methods of using the same

Cysteine-rich polypeptides and conjugates and methods of using the same

https://patents.google.com/patent/WO2018044234A1/en?inventor=Antony+KAM

Epidermal growth factor receptor (egfr) ligands

2 entries
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Past publications RSS

Past publications

Attenuation of methylglyoxal-induced glycation and cellular dysfunction in wound healing by Centella cordifolia.

Alqahtani, A. S., Li, K. M., Razmovski-Naumovski, V., Kam, A., Alam, P. and Li, G. Q. Attenuation of methylglyoxal-induced glycation and cellular dysfunction in wound healing by Centella cordifolia. Saudi J. Biol. Sci., 2021, 28(1), 813-824.

Chromatographic, Chemometric and Antioxidant Assessment of the Equivalence of Granules and Herbal Materials of Angelicae Sinensis Radix

Razmovski-Naumovski, V., Zhou, X., Wong, H.Y., Kam, A., Pearson, J. and Chan, K. Chromatographic, Chemometric and Antioxidant Assessment of the Equivalence of Granules and Herbal Materials of Angelicae Sinensis Radix. Medicines, 2020, 7(6), 35.

Synergistic study of a Danshen (Salvia Miltiorrhizae Radix et Rhizoma) and Sanqi (Notoginseng Radix et Rhizoma) combination on cell survival in EA. hy926 cells

Zhou, X., Razmovski-Naumovski, V., Kam, A., Chang, D., Li, C. G., Chan, K. and Bensoussan, A. Synergistic study of a Danshen (Salvia Miltiorrhizae Radix et Rhizoma) and Sanqi (Notoginseng Radix et Rhizoma) combination on cell survival in EA. hy926 cells. BMC Complement. Altern. Med., 2019, 19(1), 50.

Synergistic effects of Danshen (Salvia Miltiorrhizae Radix et Rhizoma) and Sanqi (Notoginseng Radix et Rhizoma) combination in angiogenesis behavior in EAhy 926 cells.

Zhou, X., Razmovski-Naumovski, V., Kam, A., Chang, D., Li, C., Bensoussan, A. and Chan, K. Synergistic effects of Danshen (Salvia Miltiorrhizae Radix et Rhizoma) and Sanqi (Notoginseng Radix et Rhizoma) combination in angiogenesis behavior in EAhy 926 cells. Medicines, 2017, 4(4), 85.

Synergistic effects of Danshen (Salvia Miltiorrhiza Radix et Rhizoma) and Sanqi (Notoginseng Radix et Rhizoma) combination in inhibiting inflammation mediators in RAW264. 7 cells

Zhou, X., Razmovski-Naumovski, V., Chang, D., Li, C., Kam, A., Low, M., Bensoussan, A. and Chan, K. Synergistic effects of Danshen (Salvia Miltiorrhiza Radix et Rhizoma) and Sanqi (Notoginseng Radix et Rhizoma) combination in inhibiting inflammation mediators in RAW264. 7 cells. Biomed Res. Int., 2016, 2016, 5758195.

27 entries
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