Lingyun Liu     Ph.D.

Assistant Professor 

Chemical and Biomolecular Engineering

 

Office: Whitby 406

Phone: (330)972-6187

Fax:      (330)972-5856

Email: lliu@uakron.edu

 

Mailing address:

200 E. Buchtel Commons

Chemical and Biomolecular Engineering

University of Akron, Akron, OH 44325-3906

 

 

 
 


           

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Ph.D. (2007)    Bioengineering, University of Washington

MS (2000)       Biomedical Engineering, Southeast University

BS (1998)        Biomedical Engineering, Southeast University

 

Research interests:

Biointerfaces

Biosensors

Biomaterials

Tissue Engineering

 

Complete Publications

Representative Publications

§         Lingyun Liu, Gang Cheng, Timothy Chao, Buddy D. Ratner, E. Helene Sage and Shaoyi Jiang, Reduced foreign body reaction to implanted biomaterials by surface treatment with oriented osteopontin, Journal of Biomaterials-Polymer Edition, In press, 2008.

§         Lingyun Liu, Buddy D. Ratner, E. Helene Sage and Shaoyi Jiang, Endothelial cell migration on surface-density gradients of fibronectin, VEGF, or both proteins, Langmuir, 2007; 23: 11168-11173.

§         Lingyun Liu, Chunlin Qin, William T. Butler, Buddy D. Ratner and Shaoyi Jiang, Controlling the orientation of bone osteopontin to modulate osteoblast adhesion via its specific binding with collagen I, Journal of Biomedical Materials Research A, 2007; 80A: 102-110.

§         Lingyun Liu, Joy G. Ghosh, John I. Clark and Shaoyi Jiang, Studies of aB crystallin subunit dynamics by surface plasmon resonance, Analytical Biochemistry, 2006; 350(2): 186-195.

§         Shenfu Chen, Lingyun Liu, Shaoyi Jiang, Strong resistance of oligo(phosphorylcholine) self-assembled monolayers to protein adsorption, Langmuir, 2006; 22(6): 2418-2421.

§         Lingyun Liu, Shengfu Chen, Cecilia M. Giachelli, Buddy D. Ratner and Shaoyi Jiang, Controlling osteopontin orientation on surfaces to modulate endothelial cell adhesion, Journal of Biomedical Materials Research A, 2005; 74A(1): 23-31.

§         Victoria Lockhart, Lingyun Liu and Shaoyi Jiang, Interactions between secreted protein, acidic and rich in cysteine (SPARC), and type I collagen identified by surface plasmon resonance biosensor, Journal of Undergraduate Research in Bioengineering, 2004; 4(2): 69-74.

§         Shengfu Chen, Lingyun Liu, Jian Zhou and Shaoyi Jiang, Controlling antibody orientation on charged self-assembled monolayers, Langmuir, 2003; 19(7): 2859-2864.

§         Jianhua Gu, Junfu Liu, Hua Lv, Yiwen Chen, Lingyun Liu, Peng Wang, Jianming Ma and Zuhong Lu, Enhancement of the sensitivity of surface plasmon resonance biosensor with colloidal gold labeling technique, Supramolecular Science, 1998; 5: 695-698.

 

Current Research Activities

The major research interests of our lab are in the areas of biomolecular interfaces, biomaterials, and biosensors. Biomolecular interfaces drive most biological processes both in vitro and in vivo. For example, they will determine the fate of implanted biomaterials and the limit of surface-based detections. The research in the lab focuses on (a) understanding and controlling interfacial phenomena and properties of biological and chemical systems at the molecular level and (b) developing and applying new biomaterials and biosensor techniques for biomedical and engineering applications.

 

 

                  (1) Molecular engineering of surfaces for SPR sensing and detection

SPR sensor, which allows for fast, real-time, quantitative and label-free detection, has been extensively used as a platform for biosensor development. Surface chemistry for the immobilization of biomolecular recognition elements is the key to the success of a sensor. The major challenges in sensing and detection are the ability of a sensor to achieve the low detection limit (i.e., high sensitivity) and to avoid false alarms (i.e., high specificity). Our lab is exploring several novel surface functionalization approaches to realize both high sensitivity and high specificity, by controlling the orientation/conformation of the ligands immobilized on a super-nonfouling background. The newly developed platforms will be used for various applications, such as food safety monitoring and early disease diagnostics.

(2) Study the behavior of cells on well-controlled engineered surfaces

The research focuses on controlling protein orientation, conformation and distribution to modulate cell behavior for biomaterials and tissue engineering applications, in which surface modification and characterization, protein-surface interactions, protein-protein interactions and protein-cell interactions are involved. To achieve biomaterials that promote normal wound healing, biomaterial surfaces must be developed that control the orientation and conformation of proteins with precision so that the body will specifically recognize them. We are exploring different approaches to control the orientation and conformation of functional proteins on various surfaces. In the preferred orientation and conformation, the functional domains of protein molecules will be presented to cells to the greatest extent and promote healing. Protein distribution, or gradient, plays an important role in cell migration. Cell migration is essential in many physiological processes such as angiogenesis, wound healing, and tumor metastasis. Particularly, angiogenesis is critical to wound healing (since the newly formed blood vessels provide nutrition and oxygen to growing tissues) and thus is critical to the success of implanted biomaterials and tissue-engineered constructs. We are studying how the gradients of extracellular matrix proteins and growth factors affect the migration of endothelial cells. Findings from this project will provide useful information for directing cell migration into tissue-engineered constructs and can be potentially used for those applications where cell migration is critical, such as angiogenesis.

 (3) Develop non-fouling surfaces/materials for biomedical applications

The development of nonfouling materials and surfaces is critical to many biomedical applications, such as biomaterials, tissue scaffolds, drug delivery carriers and biosensors. For example, a very low amount, at the scale of 1 ng/cm2, of protein adsorption to the synthetic blood vessel could lead to the platelet adhesion and accumulation, thrombosis, and therefore failure of the device. The lab is exploring several newly developed non-fouling materials, including mixed charged or zwitterionic self-assembled monolayers (SAMs) and polymers, for their resistance to protein adsorption and cell adhesion. Long-term goal of this project is on the development of drug delivery carriers and tissue scaffolds based on the novel nonfouling materials.

 

Positions Available

Several PhD student positions are available immediately in the group. Researches in the lab mainly focus on engineering biointerfaces (e.g., controlling the cell-protein-surface interactions) for biosensor, biomaterial and tissue engineering applications (e.g., disease detection, and biocompatibility enhancement). Students with Chemical Engineering degree and bio-related research experiences are preferred while those with Bioengineering / Biomedical Engineering/ Material / Polymer degree will also be considered. Research experience in one or more of the following areas is a plus: organic synthesis, SPR biosensor, surface engineering, biomaterials and tissue engineering. Assistantship will be provided. Interested applicants please email the CV, transcripts, TOEFL and GRE scores to Dr. Liu at lliu@uakron.edu.

 

Last updated: April 10, 2008