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Structured PEGs for manipulation of biological macromolecules
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Journal of Material Sciences & Engineering

ISSN: 2169-0022

Open Access

Structured PEGs for manipulation of biological macromolecules


2nd International Conference and Exhibition on Materials Science & Engineering

October 07-09, 2013 Hampton Inn Tropicana, Las Vegas, NV, USA

Kazushi Kinbara

Scientific Tracks Abstracts: J Material Sci

Abstract :

Polyethylene glycol (PEG) is one of the most popular water-soluble organic compounds, which has been widely used for biological and medicinal applications. We have been interested in structured PEGs, non-linear PEG analogues having specific two or three-dimensional molecular shapes, with the expectation that these molecules would have distinctive physical or chemical characteristics compared to the conventional linear PEGs. In order to develop structured PEGs having two- or three- dimensional molecular shapes, we have investigated synthetic methods to connect several tetraethylene glycol (TEGs) units with pentaerythritol. This molecular design strategy also enables to obtain PEG analogues in a monodisperse form, which can be a significant advantage over the intrinsically polydisperse conventional PEGs, to allow precise evaluation of their properties at a molecular level. As the first example of the structured PEG, we have developed macrocyclic triangle PEG (1) that consists of three TEG and pentaerythritol units, respectively. Interestingly, this triangle molecule exhibits hydrophilicity/hydrophobicity switching at lower temperature than the linear PEG with a comparable molecular weight. Furthermore, 1 effectively suppressed thermal aggregation of lysozyme even after 30-min heating at 90ºC, while lysozyme alone tends to denature around 80ºC to give precipitates. After the heating, lysozyme showed nearly 80% of the residual activity at 20ºC. CD and NMR spectroscopic studies revealed that, in the presence of 1, the higher-order structures of lysozyme are preserved at high temperatures, whereby the native conformation is recovered after cooling. In contrast, the linear PEGs have no such features.

Biography :

Kazushi Kinbara has completed his Ph.D. in 1996 from the University of Tokyo. In 2008, he was promoted to Professor of the Institute of Multidisciplinary Research for Advanced Materials, Tohoku University. His research interests include development of biomimetic molecules, supramolecular chemistry of macromolecules, and protein engineering.

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