Ph.D., University of Cologne, Germany and Massachusetts Institute of Technology (MIT), Cambridge, USA, 1990
M.Sc., Chemistry, University of Cologne, 1986
B.Sc., Chemistry, University of Cologne, Germany, 1983
B.Sc., Physics, University of Cologne, Germany,1980
Professor Hauser’s research interests align at the interfaces between chemistry, biomedicine, bioengineering and nanotechnology. Focus is on the development of platform technologies, using smart nanomaterials for regenerative, biomedical and environmental applications.
Her interest refers to the rational molecular design, synthesis and mechanistic understanding of novel supramolecular structures. Investigated systems include peptide-based nanostructures with an innate propensity to self-assemble to biomimetic architectures applicable for biomedical applications such as cell substrates, sensors and 3D tissue scaffolds for regenerative medicine. Bottom-up nanofabrication is a powerful tool for the development of functional tissue equivalents, organotypic tissues and devices. Moreover, these biomimetic supramolecular constructs will be used for the design and fabrication of novel organ-on-a-chip devices and disease models.
Furthermore, Professor Hauser is interested in 3D bioprinting, using supramolecular organotypic constructs to fabricate high-throughput platforms for drug screening, pathogen detection and other diagnostic purposes. Synthetic biology approaches are explored for the generation of functional biomaterial.
H. H. Susapto, D. M. Alhattab, S. A. Abdelrahman, K. M. Kahin, Z. Khan, S. Alshehri, R. Ge, M. Moretti, A.-H. Emwas, and C. A. E. Hauser, Ultrashort Peptide Bioinks Support Automated Printing of Large-Scale Constructs Assuring Long-Term Survival of Printed Tissue Constructs, Nano Letters (2021), doi.org/10.1021/acs.nanolett.0c04426
Y. Loo, Y. S. Chan, I. Szczerbinska, B. C. P. Tan, A. C. A. Wan, H. H. Ng, and C. A. E. Hauser, "A Chemically Well-Defined, Self-Assembling 3D Substrate for Long Term Culture of Human Pluripotent Stem Cells", ACS Applied Bio Materials 2,4 (2019) 1406-1412
K. H. Chan, W. H. Lee, M. Ni, Y. Loo and C. A. E. Hauser, "C-Terminal residue of Ultrashort Peptides Impacts on Molecular Self-assembly, Hydrogelation, and Interaction with Small-Molecule Drugs," Scientific Reports 8 (2018), 17127
K. H. Chan, B. Xue, R. C. Robinson and C. A. E. Hauser, " Systematic Moiety Variations of Ultrashort Peptides Produce Profound Effects on Self-Assembly, Nanostructure Formation, Hydrogelation, and Phase Transition," Scientific Reports 7 (2017), 12897
Cima, S. L. Kong, D. Sengupta, I. B. Tan, W. M. Phyo, D. Lee, M. Hu, C. Iliescu, I. Alexander, W. L. Goh, M. Rahmani, N.-A. M. Suhaimi, J. H. Vo, J. A. Tai, J. H. Tan, C. Chua, R. Ten, M. H. Chew, C. A.E. Hauser, R. M. van Dam, W.-Y. Lim, S. Prabhakar, B. Lim, P. K. Koh, P. Robson, J. Y. Ying, A. M. Hillmer, and M.-H. Tan, "Tumor-derived circulating endothelial cell clusters in colorectal cancer", Science Translational Medicine 8 (2016) 345ra89
W.Y. Seow, G. Salgado, E.B. Lane, and C.A.E. Hauser, "Transparent crosslinked ultrashort peptide hydrogels as a carrier dressing with high shape fidelity to accel-erate healing of full-thickness excision wounds," Scientific Reports 6 (2016), 32670
Y. Loo, A. Lakshmanan, M. Ni, L. L. Toh, S. Wang, and C. A.E. Hauser, "Peptide Bioink: Self-Assembling Nanofibrous Scaffolds for 3D Organotypic Cultures," Nano Letters 15 (2015) 6919-6925
J. Smadbeck, K. H. Chan, G. A. Khoury, B. Xue, R. C. Robinson, C. A. E. Hauser, and C. A. Floudas, "De Novo Design and Experimental Characterization of Ultrashort Self-Associating Peptides," PLOS Computational Biology 10  (2014) e1003718
M. R. Reithofer, A. Lakshmanan, A. T. K. Ping, J. M. Chin and C.A.E. Hauser, "In situ Synthesis of Size-Controlled, Stable Silver Nanoparticles within Ultrashort Peptide Hydrogels and their Anti-Bacterial Properties," Biomaterials, 35 (2014) 7535-7542
M. R. Reithofer, K.-H. Chan, A. Lakshmanan, D. H. Lam, A. Mishra, B. Gopalan, M. Joshi, S. Wang, and C. A. E. Hauser, "Ligation of Anti-Cancer Drugs to Self-Assembling Ultrashort Peptides by Click Chemistry for Localized Therapy," Chemical Science, 5 (2014) 625-630
Y. Loo, Y. C. Wong, E. Z. Cai, C. H. Ang, A. Raju, A. Lakshmanan, A. G. W. Koh, H. J. Zhou, T. C. Lim, S. M. Moochhala, and C. A.E. Hauser, "Ultrashort Peptide Nanofibrous Hydrogels for the Acceleration of Healing of Burn Wounds," Bio-materials, 35 (2014) 4805-14
W. Y. Seow and C. A. E. Hauser, "Tunable Mechanical Properties of Ultrasmall Peptide Hydrogels by Crosslinking and Functionalization to Achieve the 3D Distribution of Cells," Advanced Healthcare Materials, 2 (2013) 1219-1223
Lakshmanan, D. W. Cheong, A. Accardo, E. Di Fabrizio, C. Riekel, and C. A. E. Hauser, "Aliphatic Peptides Show Similar Self-Assembly to Amyloid Core Sequences, Challenging the Importance of Aromatic Interactions in Amyloidosis," PNAS, 110 (2013) 519-524
Mishra, Y. Loo, R. Deng, Y. J. Chuah, H. T. Hee, J. Y. Ying and C. A. E. Hauser, "Ultrasmall Natural Peptides Self-Assemble to Strong Temperature-Resistant Helical Fibers in Scaffolds Suitable for Tissue Engineering," NanoToday, 6 (2011) 232-239
C.A.E. Hauser, R. Deng, A. Mishra, Y. Loo, U. Khoe, F. Zhuang, D.W. Cheong, A. Accardo, M.B. Sullivan, C. Riekel, J.Y. Ying, and U.A. Hauser, "Natural Tri- to Hexapeptides Self-Assemble in Water to Amyloid β-type Fiber Aggregates by Unexpected α-Helical Intermediate Structures," PNAS, 108 (2011) 1361–1366