The proposal is aimed to improve the pharmacological effects of low-molecular weight heparins (LMWH). This project is a collaborative effort of four research groups, including Dr. Jian Liu (University of North Carolina) Dr. Robert Linhardt (Rensselaer Polytechnic Institute), Dr. Edward Harris (University of Nebraska, Lincoln) and Dr. Jawed Fareed (Loyola University Medical Center). LWMH is a widely used anticoagulant drug to treat thrombotic disorders. The currently marketed LMWH drugs are a mixture of sulfated poly-/oligo-saccharides, which are vulnerable to contamination and batch-to-batch variability. We plan to synthesize structurally homogeneous LMWH to eliminate the structural heterogeneity. The new LMWH constructs should display consistent anticoagulant activity, improved sensitivity to protamine neutralization, and controlled metabolic pathway. The synthesis of homogeneous LMWH will be completed using a chemo enzymatic approach. The pharmacological effects of the products will be evaluated in mouse and primate models. The success of this project will optimize the structures of heparin-based drugs with improved safety and efficacy.

Public Health Relevance

Low-molecular weight heparin is a commonly used anticoagulant drug. Currently, low-molecular weight heparin is prepared from the degradation of heparin that is isolated from animal tissues. It has been known that animal-sourced heparin is vulnerable to contamination. This project is aimed to design and synthesize structurally homogeneous low-molecular weight heparins to improve its pharmacological effects as well as eliminate the need for animal-sourced heparin.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL094463-06
Application #
8711536
Study Section
Synthetic and Biological Chemistry A Study Section (SBCA)
Program Officer
Sarkar, Rita
Project Start
2009-02-13
Project End
2017-05-31
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
6
Fiscal Year
2014
Total Cost
$374,845
Indirect Cost
$66,825
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Pharmacy
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Pellock, Samuel J; Walton, William G; Biernat, Kristen A et al. (2018) Three structurally and functionally distinct ?-glucuronidases from the human gut microbe Bacteroides uniformis. J Biol Chem 293:18559-18573
Xu, Ding; Arnold, Katelyn; Liu, Jian (2018) Using structurally defined oligosaccharides to understand the interactions between proteins and heparan sulfate. Curr Opin Struct Biol 50:155-161
Stancanelli, Eduardo; Elli, Stefano; Hsieh, Po-Hung et al. (2018) Recognition and Conformational Properties of an Alternative Antithrombin Binding Sequence Obtained by Chemoenzymatic Synthesis. Chembiochem :
Xiao, Yiming; Li, Miaomiao; Larocque, Rinzhi et al. (2018) Dimerization interface of osteoprotegerin revealed by hydrogen-deuterium exchange mass spectrometry. J Biol Chem 293:17523-17535
Nam, Eon Jeong; Hayashida, Kazutaka; Aquino, Rafael S et al. (2017) Syndecan-1 limits the progression of liver injury and promotes liver repair in acetaminophen-induced liver injury in mice. Hepatology 66:1601-1615
Wang, Haisheng; He, Wenqin; Jiang, Peixia et al. (2017) Construction and functional characterization of truncated versions of recombinant keratanase II from Bacillus circulans. Glycoconj J 34:643-649
Pollet, Rebecca M; D'Agostino, Emma H; Walton, William G et al. (2017) An Atlas of ?-Glucuronidases in the Human Intestinal Microbiome. Structure 25:967-977.e5
Zhao, Jing; Liu, Xinyue; Malhotra, Anju et al. (2017) Novel method for measurement of heparin anticoagulant activity using SPR. Anal Biochem 526:39-42
Zhang, Xing; Pagadala, Vijayakanth; Jester, Hannah M et al. (2017) Chemoenzymatic synthesis of heparan sulfate and heparin oligosaccharides and NMR analysis: paving the way to a diverse library for glycobiologists. Chem Sci 8:7932-7940
Li, Jine; Su, Guowei; Liu, Jian (2017) Enzymatic Synthesis of Homogeneous Chondroitin Sulfate Oligosaccharides. Angew Chem Int Ed Engl 56:11784-11787

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