Check our Youtube Channel
https://www.youtube.com/channel/UCTtoWa4_sYRVAJ_v-qQpE6g
![Mark omaha PA nanofiber (1).jpg](https://static.wixstatic.com/media/e249ce_6974b7d8c14b4a59b345e5fd4161b32f~mv2.jpg/v1/crop/x_46,y_79,w_978,h_611/fill/w_351,h_218,al_c,q_80,usm_0.66_1.00_0.01,enc_avif,quality_auto/Mark%20omaha%20PA%20nanofiber%20(1).jpg)
![nanofiber PEG3b.jpg](https://static.wixstatic.com/media/e249ce_4881ed7f555a428999c2f85e221c330a~mv2.jpg/v1/crop/x_118,y_12,w_906,h_729/fill/w_338,h_270,al_c,q_80,usm_0.66_1.00_0.01,enc_avif,quality_auto/nanofiber%20PEG3b.jpg)
Biomaterials​
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Our work in biomaterials revolves around the peptide amphiphiles (PAs), self-assembling molecules that form nanostructures in water. The current projects are described below.
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1) Antibacterial nanostructures. We have recently found the morphology of PA-based nanostructures is a key parameter in the antimicrobial action of these systems (DOI: 10.1021/acsami.8b17808). The mechanism of action of the nanostructures is related to their ability to disrupt the bacterial membrane. We are currently fine-tuning parameters such as size, hydrophobic ratio, and zeta potential to find a potent nanostructure with low toxicity. In addition, we try to incorporate know antibiotics within the structure of the PAs to develop hybrid systems with synergistic potential.
https://pubs.acs.org/doi/abs/10.1021/acsami.8b17808
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2) New self-assembling systems. We are exploring the effect that various solubilizing groups such as polyamines, sugars, and DNA-base pairs have in the self-assembling properties. We recently published a paper detailing the effect that various amines have in the morphology, cell toxicity, and chemical and metabolic stability of peptide-based systems. Our collaborators, Dr. Mario Tagliazucchi and his group, are developing theoretical tools to understand the behavior of these new systems.
https://onlinelibrary.wiley.com/doi/abs/10.1002/mabi.201700096
https://pubs.rsc.org/en/content/articlelanding/2018/sm/c8sm00096d/unauth#!divAbstract
https://pubs.acs.org/doi/abs/10.1021/acs.jpcc.9b04280
https://pubs.acs.org/doi/abs/10.1021/acs.jpcb.0c01301
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3) Cancer-targeting nanostructures. We are developing nanostructures of various morphologies to detect and treat colon and prostate cancer (therasnostic systems).
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![Flow.png](https://static.wixstatic.com/media/e249ce_c591bb2b27be4852861409239c0b98b3~mv2_d_1470_1264_s_2.png/v1/crop/x_221,y_194,w_964,h_650/fill/w_288,h_194,al_c,q_85,usm_0.66_1.00_0.01,enc_avif,quality_auto/Flow.png)
![phosphine in tail sphere.jpg](https://static.wixstatic.com/media/e249ce_a79813bfba8249ec80aead6d6ec43a2d~mv2.jpg/v1/crop/x_113,y_4,w_817,h_764/fill/w_217,h_203,al_c,q_80,usm_0.66_1.00_0.01,enc_avif,quality_auto/phosphine%20in%20tail%20sphere.jpg)
![linker bioactivity necks slice3.jpg](https://static.wixstatic.com/media/e249ce_38591caa1f9548889cfaceb4b402d19d~mv2.jpg/v1/fill/w_366,h_273,al_c,q_80,usm_0.66_1.00_0.01,enc_avif,quality_auto/linker%20bioactivity%20necks%20slice3.jpg)
Flow cytometry analysis. Cell membrane disruption of S. aureus JE2 MRSA treated with PA 4 (C18K5) and PA 7 (C18K-K5) at MIC was determined by an increase in fluorescent intensity of PI. Negative control - No PA; PA 4 at 8 μg/mL; PA 7 at 8 μg/mL and PA 12 (C18R5) at 16 μg/mL. Treatment with EtOH 70% was used as positive control.