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 | Biography
Shuguang Zhang is the Associate Director of the Center for Biomedical
Engineering at Massachusetts Institute of Technology. He received his
Ph.D. in Biochemistry and Molecular Biology from University of California
at Santa Barbara. He received his B.S. from Sichuan University in China.
He was a past American Cancer Society Fellow at MIT. He is a Visiting
Professor at Tsinghua (Qinghua) University in Beijing and at Sichuan
University in Chengdu, China. He is a consultant for Acorda Therapeutics
in New York; and a Scientific Advisor for Mitsubishi Chemical Corporation
Research Center in Yokohama, Japan. He is members of AAAS, American
Society of Biochemistry and molecular Biology (ASBMB), The Human Genome
Organization Americas (HUGO), the Protein Society, New York Academy of
Sciences, The International Society for the Study of Origin of Life (ISSOL)
and the honorary society of Sigma Xi. |
 | Research Interests
Biological self-assembly systems lie at the interface between molecular
biology, chemistry, materials science and engineering. The key elements in
molecular self-assembly are chemical complementarity and structural
compatibility. Several distinctive types of peptides have been developed.
Type I peptides undergo intermolecular self-assembly to form a gel matrix
that can be used for as a scaffold tissue engineering. Type II peptides
undergo structural transformations for intermolecular and intramolecular
self-assembly. Analysis of the molecular switch will provide us insight
into the onset of protein conformational diseases. Type III peptides
undergo self-assembly on to surfaces to form molecular hook and molecular
Volcro that interact with other molecules and to control cell patterns.
Type IV peptides undergo assembly with nucleic acids to promote gene
delivery. The self-assembling peptide systems are simple, versatile and
easy to produce. These systems represent a significant advancement in the
molecular engineering of protein fragments for diverse technological
innovations. |
 | Selected Publications
1. Zhang, S., Holmes, T., Lockshin, C. & Rich, A (1993), Spontaneous
assembly of a self-complementary oligopeptide to form a stable macroscopic
membrane. Proc. Natl. Acad. Sci. USA 90, 3334-3338.
2. Shuguang Zhang and Martin Egli (1995) A proposed complementary
pairing mode between single-stranded nucleic acids and b-stranded peptides:
A possible pathway for generating complex biological molecules. Complexity
1, 49-56.
3. Zhang, S., Holmes, T., DiPersio, M., Hynes, R. O., Su, X., & Rich,
A (1995) Self-complementary oligopeptide matrices support mammalian cell
attachment. Biomaterials 16, 1385-1393.
4. Zhang, S & Rich, A. (1997) Direct conversion of an oligopeptide
from a b-sheet to an a-helix: A Model for amyloid formation. Proc. Natl.
Acad. Sci. USA 94, 23-28.
5. Zhang, S., Yan, L. Altman, M., Lassle, M., Nugent, H., Frankel, F.,
Lauffenburger, D., Whitesides, G. W. & Rich, A. (1999) Biological surface
engineering: A simple system for cell pattern formation. Biomaterials (In
press). |
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