Literature DB >> 22034431

Chemoenzymatic synthesis of homogeneous ultralow molecular weight heparins.

Yongmei Xu1, Sayaka Masuko, Majde Takieddin, Haoming Xu, Renpeng Liu, Juliana Jing, Shaker A Mousa, Robert J Linhardt, Jian Liu.   

Abstract

Ultralow molecular weight (ULMW) heparins are sulfated glycans that are clinically used to treat thrombotic disorders. ULMW heparins range from 1500 to 3000 daltons, corresponding from 5 to 10 saccharide units. The commercial drug Arixtra (fondaparinux sodium) is a structurally homogeneous ULMW heparin pentasaccharide that is synthesized through a lengthy chemical process. Here, we report 10- and 12-step chemoenzymatic syntheses of two structurally homogeneous ULMW heparins (MW = 1778.5 and 1816.5) in 45 and 37% overall yield, respectively, starting from a simple disaccharide. These ULMW heparins display excellent in vitro anticoagulant activity and comparable pharmacokinetic properties to Arixtra, as demonstrated in a rabbit model. The chemoenzymatic approach is scalable and shows promise for a more efficient route to synthesize this important class of medicinal agent.

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Year:  2011        PMID: 22034431      PMCID: PMC3425363          DOI: 10.1126/science.1207478

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  28 in total

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Journal:  Circulation       Date:  2007-07-31       Impact factor: 29.690

2.  Oversulfated chondroitin sulfate is a contaminant in heparin associated with adverse clinical events.

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Journal:  Nat Biotechnol       Date:  2008-04-23       Impact factor: 54.908

3.  Determination of the substrate specificities of N-acetyl-d-glucosaminyltransferase.

Authors:  Miao Chen; Arlene Bridges; Jian Liu
Journal:  Biochemistry       Date:  2006-10-10       Impact factor: 3.162

Review 4.  Beyond heparin and warfarin: the new generation of anticoagulants.

Authors:  Jeffrey I Weitz; Lori-Ann Linkins
Journal:  Expert Opin Investig Drugs       Date:  2007-03       Impact factor: 6.206

5.  Enzymatic redesigning of biologically active heparan sulfate.

Authors:  Jinghua Chen; Fikri Y Avci; Eva M Muñoz; Lynda M McDowell; Miao Chen; Lars C Pedersen; Lijuan Zhang; Robert J Linhardt; Jian Liu
Journal:  J Biol Chem       Date:  2005-10-31       Impact factor: 5.157

Review 6.  Triggers, targets and treatments for thrombosis.

Authors:  Nigel Mackman
Journal:  Nature       Date:  2008-02-21       Impact factor: 49.962

7.  Solution structures of chemoenzymatically synthesized heparin and its precursors.

Authors:  Zhenqing Zhang; Scott A McCallum; Jin Xie; Lidia Nieto; Francisco Corzana; Jesús Jiménez-Barbero; Miao Chen; Jian Liu; Robert J Linhardt
Journal:  J Am Chem Soc       Date:  2008-09-04       Impact factor: 15.419

8.  Using an enzymatic combinatorial approach to identify anticoagulant heparan sulfate structures.

Authors:  Jinghua Chen; Courtney L Jones; Jian Liu
Journal:  Chem Biol       Date:  2007-09

9.  Engineering sulfotransferases to modify heparan sulfate.

Authors:  Ding Xu; Andrea F Moon; Danyin Song; Lars C Pedersen; Jian Liu
Journal:  Nat Chem Biol       Date:  2008-01-27       Impact factor: 15.040

10.  Chemoenzymatic synthesis with distinct Pasteurella heparosan synthases: monodisperse polymers and unnatural structures.

Authors:  Alison E Sismey-Ragatz; Dixy E Green; Nigel J Otto; Martin Rejzek; Robert A Field; Paul L DeAngelis
Journal:  J Biol Chem       Date:  2007-07-11       Impact factor: 5.157

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  122 in total

1.  Directing the biological activities of heparan sulfate oligosaccharides using a chemoenzymatic approach.

Authors:  Yongmei Xu; Zhen Wang; Renpeng Liu; Arlene S Bridges; Xuefei Huang; Jian Liu
Journal:  Glycobiology       Date:  2011-08-11       Impact factor: 4.313

2.  Potent direct inhibitors of factor Xa based on the tetrahydroisoquinoline scaffold.

Authors:  Rami A Al-Horani; Akul Y Mehta; Umesh R Desai
Journal:  Eur J Med Chem       Date:  2012-06-23       Impact factor: 6.514

3.  Chemoenzymatic synthesis of heparin oligosaccharides with both anti-factor Xa and anti-factor IIa activities.

Authors:  Yongmei Xu; Elizabeth H Pempe; Jian Liu
Journal:  J Biol Chem       Date:  2012-07-06       Impact factor: 5.157

4.  Controlled Chemoenzymatic Synthesis of Heparan Sulfate Oligosaccharides.

Authors:  Weigang Lu; Chengli Zong; Pradeep Chopra; Lauren E Pepi; Yongmei Xu; I Jonathan Amster; Jian Liu; Geert-Jan Boons
Journal:  Angew Chem Int Ed Engl       Date:  2018-03-30       Impact factor: 15.336

5.  FGF-FGFR signaling mediated through glycosaminoglycans in microtiter plate and cell-based microarray platforms.

Authors:  Eric Sterner; Luciana Meli; Seok-Joon Kwon; Jonathan S Dordick; Robert J Linhardt
Journal:  Biochemistry       Date:  2013-12-06       Impact factor: 3.162

Review 6.  Expedient Synthesis of Core Disaccharide Building Blocks from Natural Polysaccharides for Heparan Sulfate Oligosaccharide Assembly.

Authors:  Nitin J Pawar; Lei Wang; Takuya Higo; Chandrabali Bhattacharya; Pavan K Kancharla; Fuming Zhang; Kedar Baryal; Chang-Xin Huo; Jian Liu; Robert J Linhardt; Xuefei Huang; Linda C Hsieh-Wilson
Journal:  Angew Chem Int Ed Engl       Date:  2019-11-06       Impact factor: 15.336

7.  3-O sulfation of heparin leads to hepatotropism and longer circulatory half-life.

Authors:  Colton M Miller; Yongmei Xu; Katrina M Kudrna; Blake E Hass; Brianna M Kellar; Andrew W Egger; Jian Liu; Edward N Harris
Journal:  Thromb Res       Date:  2018-05-17       Impact factor: 3.944

8.  Chemoenzymatic synthesis and structural characterization of 2-O-sulfated glucuronic acid-containing heparan sulfate hexasaccharides.

Authors:  Po-Hung Hsieh; Yongmei Xu; David A Keire; Jian Liu
Journal:  Glycobiology       Date:  2014-04-25       Impact factor: 4.313

Review 9.  Understanding the substrate specificity of the heparan sulfate sulfotransferases by an integrated biosynthetic and crystallographic approach.

Authors:  Jian Liu; Andrea F Moon; Juzheng Sheng; Lars C Pedersen
Journal:  Curr Opin Struct Biol       Date:  2012-07-26       Impact factor: 6.809

10.  Molecular mechanism of substrate specificity for heparan sulfate 2-O-sulfotransferase.

Authors:  Chunhui Liu; Juzheng Sheng; Juno M Krahn; Lalith Perera; Yongmei Xu; Po-Hung Hsieh; Wenfang Dou; Jian Liu; Lars C Pedersen
Journal:  J Biol Chem       Date:  2014-03-20       Impact factor: 5.157

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