Skip Navigation


Journal of Biochemistry Advance Access originally published online on May 7, 2008
Journal of Biochemistry 2008 144(2):207-213; doi:10.1093/jb/mvn060
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
144/2/207    most recent
mvn060v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Tan, H.
Right arrow Articles by Wang, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tan, H.
Right arrow Articles by Wang, F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2008 The Japanese Biochemical Society

Characterization and Secondary Structure Analysis of Endostatin Covalently Modified by Polyethylene Glycol and Low Molecular Weight Heparin

Haining Tan1,2, Shenglin Yang1, You Feng1, Chunhui Liu1,2, Jichao Cao1, Guoying Mu3 and Fengshan Wang1,2,*

1Institute of Biochemical and Biotechnological Drug, School of Pharmaceutical Science, Shandong University; 2National Glycoengineering Research Center, Shandong University; and 3Jinan Central Hospital and Clinical Medical College of Shandong University, Jinan, China

*To whom correspondence should be addressed. Tel: 86-531-88380288, Fax: 86-531-88382548, E-mail: fswang{at}sdu.edu.cn

Received March 4, 2008; Accepted April 15, 2008


   Abstract

Endostatin (ES), as an angiogenesis inhibitor, has been approved by the State Food and Drug Administration (SFDA) in China for the treatment of patients with non-small-cell lung cancer. However, as a protein drug, there are a lot of obstacles on its clinical application, such as need of high dose to maintain its efficacy, expensive and poor stability, etc and limits its clinical use. In order to overcome these shortcomings, we chemically modified ES by polyethylene glycol and low molecular weight heparin (LMWH), respectively. The changes of the secondary structure of the modified products were studied by Fourier transform infrared spectroscopy and Circular dichroism spectra to obtain better ES derivatives. Our study demonstrated that the modified products have a better heat tolerance than ES towards. The result of secondary structure analysis suggests the percentage of β-turn in whole protein is an important factor on the activity and heat stability and ES modified by LMWH can maintain higher activity and its secondary structure.

Key Words: chemical modification, endostatin, low molecular weight heparin, polyethylene glycol, stability, structure

Abbreviations: ATR-FTIR, attenuated total reflectance Fourier transform infrared; ES, endostatin; FTIR, Fourier transform infrared spectroscopy; HUVEC, human umbilical vein endothelial cell; KRS-5, thallium bromoiodide; LMWH, low molecular weight heparin; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazoliumbromide; PEG, polyethylene glycol; TNBS, 2,4,6-trinitrobenzene sulphonic acid


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.