IRG-II

SIMPLE ENGINEERED BIOLOGICAL MOTIFS FOR COMPLEX HYDROGEL FUNCTION


 


GOALS
This multidisciplinary team sits at the intersection of science and engineering, and seeks to establish the fundamental knowledge base needed to inspire cutting-edge practical applications of complex biological hydrogels. Such materials are abundantly used in nature, with properties that are unachieved by current synthetic materials. These include the ability to selectively filter complex solutions while retaining unique self-healing capabilities, to function as physical barriers that allow the penetration of bacteria while suppressing biofilm formation, and to maintain highly compressive states while providing a high level of lubrication. The goal of this IRG is to gain quantitative insight into, and predictive capability of, the molecular mechanisms that govern the unique structure and property combinations of complex biological hydrogels.

We will use this fundamental knowledge to guide the synthesis, fabrication and evaluation of next generation materials with potentially wide engineering implications, such as the design of self-healing filtration systems for water and food purification, new antimicrobial coatings for implants, or cartilage substitutes with high durability and lubrication capacity.

Current synthetic approaches are largely unable to recapitulate the sophisticated materials properties found in complex biological hydrogels. One reason for this is our lack of mechanistic understanding of the microscopic structures and chemistries that build and regulate natural hydrogels. This IRG will systematically analyze selected critical factors involved in complex biological hydrogel function, using an interdisciplinary set of tools that the investigators bring together, including the isolation and reconstitution of natural hydrogels, the chemical synthesis of bio-inspired polymers, molecular tools for controlling polymerization, and the state-of-the-art materials properties analysis, and molecular modeling. In particular, this IRG will focus on the study of three basic molecular elements that are found in complex biological hydrogels: a) conserved domains with repeating sequences, b) reversible/dynamic crosslinks, and c) variable glycosylation patterns.

 

PEOPLE

Katharina Ribbeck
(co-leader)
BioE
Bradley Olsen
(co-leader)
ChemE
Patrick Doyle
Chem E
Niels Holten-Andersen
DMSE
Jeremiah Johnson
Chemistry
Alan Grodzinsky
Bio E / EECS / Mech E
Paula Hammond
Chem E
Timothy Lu
EECS / Bio E
Gareth H. McKinley
MechE

 

HIGHLIGHTS
2018
How Mucus Keeps You Healthy

The Gels, Elastomers, and Networks Experience (GENE)
 

2017
Understanding Loops in Polymer Networks Results in an Improved Theory for Rubbery Materials

Using Light to Control the Viscoelastic Mechanical Properties of Gel-Like Materials

2016
Biochemical mechanisms to control gel crosslinking and permeability

2015
Bio-Inspired Gels show promise as self-healing materials with properties controlled by metal ions

 

PUBLICATIONS
2018
Bansil, R. and Turner, B.S.* "The biology of mucus: composition, synthesis and organization." Advanced Drug Delivery Reviews, 124: 3-15, January 2018. <DOI: 10.1016/j.addr.2017.09.023>

Sing, M.K., Burghardt, W.R., and Olsen, B.D. "Influence of end-block dynamics on deformation behavior of thermoresponsive elastin-like polypeptide hydrogels." Macromolecules, 51(8): 2951-2960, April 2018. <DOI:  10.1021/acs.macromol.8b00002>

 

2017
Wagner, C.E., Turner, B.S., Rubinstein, M., McKinley, G.H., and Ribbeck, K.  "A rheological study of the association and dynamics of MUC5AC gels." Biomacromolecules, 18(11): 3654-3664 SI, November 2017. DOI: 10.1021/acs.biomac.7b00809

Bajpayee, A.G., De la Vega, R.E., Scheu, M., Varady, N.H., Yannatos, I.A., Brown, L.A., Krishnan, Y., Fitzsimons, T.J., Bhattacharya, P., Frank, E.H., Grodzinsky, A.J., and Porter, R.M. “Sustained intra-cartilage delivery of low dose dexamethasone using a cationic carrier for treatment of post traumatic osteoarthritis.” European Cells & Materials, 34: 341-364, July-December 2017. DOI: 10.22203/eCM.v034a21

Cheng, L.C., Hsiao, L.C., and Doyle, P.S. “Multiple particle tracking study of thermally-gelling nanoemulsions.” Soft Matter, 13(37): 6606-6619, October 2017. DOI: 10.1039/c7sm01191a

Chen, L., Wang, K.X., and Doyle, P.S. “Effect of internal architecture on microgel deformation in microfluidic constrictions.” Soft Matter, 13(9): 1920-1928, 2017.DOI: 10.1039/c6sm02674e

Hsiao, L.C., Badruddoza, A.Z.M., Cheng, L.C., and Doyle, P.S. “3D printing of self-assembling thermoresponsive nanoemulsions into hierarchical mesostructured hydrogels.” Soft Matter, 13(5): 921-929, February 2017. DOI: 10.1039/c6sm02208

Kim, J.J., Bong, K.W., Reategui, E., Irimia, D., and Doyle, P.S. “Porous microwells for geometry-selective, large-scale microparticle arrays.” Nature Materials, 16(1): 139-146, January 2017. DOI: 10.1038/NMAT4747

Grindy, S.C. and Holten-Andersen, N. “Bio-inspired metal-coordinate hydrogels with Programmable viscoelastic material functions controlled by longwave UV light.” Soft Matter, 2017. DOI: 10.1039/c7sm00617a

Samad, T., Billings, N., Birjiniuk, A., Crouzier, T., Doyle, P.S. and Ribbeck, K. “Swimming bacteria promote dispersal of non-motile staphylococcal species.” International Society for Microbial Ecology Journal, 1-5: 1751-7362/17, April 2017. DOI: 10.1038/ismej.2017.23

Bajpayee, A.G., and Grodzinsky, A.J. “Cartilage-targeting drug delivery: Can electrostatic interactions help?” Nature Reviews Rheumatology, 13(3): 183-193, March 2017. DOI: 10.1038/nrrheum.2016.210

Grindy, S.C., Lenz, M., and Holten-Andersen, N. “Engineering elasticity and relaxation time in metal-coordinate cross-linked hydrogels.” Macromolecules, 49(21): 8306-8312, November 2016. DOI: 10.1021/acs.macromol.6b01523

Witten, J. and Ribbeck, K. “The particle in the spider's web: transport through biological hydrogels.” Nanoscale, 9(24): 8080-8095, June 2017. <DOI: 10.1039/c6nr09736g>

Samad, T., Billings, N., Birjiniuk, A., Crouzier, T., Doyle, P.S., and Ribbeck, K. “Swimming bacteria promote dispersal of non-motile staphylococcal species.” ISME Journal, 11(8): 1933-1937, August 2017. <DOI: 10.1038/ismej.2017.23>

 

Chen, W.G., Witten, J., Grindy, S.C., Holten-Andersen, N., and Ribbeck, K.  “Charge Influences Substrate Recognition and Self-Assembly of Hydrophobic FG Sequences.“ Biophysical Journal, 113(9): 2088-2099, November 2017. <DOI: 10.1016/j.bpj.2017.08.058>

 

2016
Mozhdehi, D., Neal, J.A., Grindy, S.C., Cordeau, Y., Ayala, S., Holten-Andersen, N., and Guan, Z.B. “Tuning dynamic mechanical response in metallopolymer networks through simultaneous control of structural and temporal properties of the networks.” Macromolecules, 49(17): 6310-6321, September 2016. DOI: 10.1021/acs.macromol.6b01626

Tang, S.C. and Olsen, B.D. “Relaxation processes in supramolecular metallogels based on histidine-nickel coordination bonds.” Macromolecules, 49(23): 9163-9175, December 2016. DOI: 10.1021/acs.macromol.6b01618

Chen, L. An, H.Z., Haghgooie, R., Shank, A.T., Martel, J.M., Toner, M., and Doyle, P.S. “Flexible octopus-shaped hydrogel particles for specific cell capture.” Small, 12(15): 2001-2008, April 2016. DOI: 10.1002/smll.201600163

Tang, S.C., Habicht, A., Li, S.L., Seiffert, S., and Olsen, B.D. “Self-diffusion of associating star-shaped polymers.” Macromolecules, 49(15): 5599-5608, August 2016. DOI: 10.1021/acs.macromol.6b00959

Zhong, M.J., Wang, R., Kawamoto, K., Olsen, B.D., and Johnson, J.A. “Quantifying the impact of molecular defects on polymer network elasticity.” Science, 353(6305): 1264-1268, September 2016. DOI: 10.1126/science.aag0184

?>