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2016 Fiscal Year Final Research Report

Development of structured PEGs and applications to protein stabilization

Research Project

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Project/Area Number 26410170
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Bio-related chemistry
Research InstitutionTokyo Institute of Technology (2015-2016)
Tohoku University (2014)

Principal Investigator

Muraoka Takahiro  東京工業大学, 生命理工学院, 助教 (70509132)

Project Period (FY) 2014-04-01 – 2017-03-31
Keywordsポリエチレングリコール / 凝集抑制効果 / 熱応答性 / 両親媒性分子 / 大環状分子
Outline of Final Research Achievements

As a series of polyethylene glycol (PEG) analogues with structured macrocyclic morphology, PEGs with digonal to hexagonal structures were synthesized and their properties were evaluated. At room temperature, the macrocyclic PEG analogues showed higher hydrophobicity than the corresponding linear PEGs, and the hydrophobicity continuously increased with the ring size. At 70 °C, on the other hand, a topological effect was observed in the relationship between the molecular structure and hydrophobicity.
Amphiphilic PEGs bearing phenyl group at the end of PEG with different chain length were also developed. Phenyl octaethylene glycol showed higher protein aggregation suppression effect than phenyl tetraethylene glycol.

Free Research Field

生体関連化学

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Published: 2018-03-22  

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