Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 96

1.

Convergent chemical synthesis of [lysine(24,38,83)] human erythropoietin.

Liu S, Pentelute BL, Kent SB.

Angew Chem Int Ed Engl. 2012 Jan 23;51(4):993-9. doi: 10.1002/anie.201106060. Epub 2011 Dec 16. No abstract available.

2.

At last: erythropoietin as a single glycoform.

Wang P, Dong S, Brailsford JA, Iyer K, Townsend SD, Zhang Q, Hendrickson RC, Shieh J, Moore MA, Danishefsky SJ.

Angew Chem Int Ed Engl. 2012 Nov 12;51(46):11576-84. doi: 10.1002/anie.201206090. Epub 2012 Sep 25. No abstract available.

3.

Diaminodiacid-based solid-phase synthesis of peptide disulfide bond mimics.

Cui HK, Guo Y, He Y, Wang FL, Chang HN, Wang YJ, Wu FM, Tian CL, Liu L.

Angew Chem Int Ed Engl. 2013 Sep 2;52(36):9558-62. doi: 10.1002/anie.201302197. Epub 2013 Jun 26. No abstract available.

PMID:
23804284
4.

Chemical synthesis of an erythropoietin glycoform containing a complex-type disialyloligosaccharide.

Murakami M, Okamoto R, Izumi M, Kajihara Y.

Angew Chem Int Ed Engl. 2012 Apr 10;51(15):3567-72. doi: 10.1002/anie.201109034. Epub 2012 Feb 3. No abstract available.

PMID:
22307754
5.

Probing the stability of nonglycosylated wild-type erythropoietin protein via reiterative alanine ligations.

Brailsford JA, Danishefsky SJ.

Proc Natl Acad Sci U S A. 2012 May 8;109(19):7196-201. doi: 10.1073/pnas.1202762109. Epub 2012 Apr 12.

6.

Synthesis and circular dichroism study of the human salivary proline-rich protein IB7.

Simon C, Pianet I, Dufourc EJ.

J Pept Sci. 2003 Feb;9(2):125-31.

PMID:
12630698
7.
8.

A convenient preparation of N (ε)-methyl-L-lysine derivatives and its application to the synthesis of histone tail peptides.

Chi H, Islam MS, Nsiama TK, Kato T, Nishino N.

Amino Acids. 2014 May;46(5):1305-11. doi: 10.1007/s00726-014-1690-6. Epub 2014 Feb 23.

PMID:
24562477
9.

Chemical synthesis of erythropoietin glycoforms for insights into the relationship between glycosylation pattern and bioactivity.

Murakami M, Kiuchi T, Nishihara M, Tezuka K, Okamoto R, Izumi M, Kajihara Y.

Sci Adv. 2016 Jan 15;2(1):e1500678. doi: 10.1126/sciadv.1500678. eCollection 2016 Jan 15.

10.

Peptide dendrimers based on polyproline helices.

Crespo L, Sanclimens G, Montaner B, Pérez-Tomás R, Royo M, Pons M, Albericio F, Giralt E.

J Am Chem Soc. 2002 Jul 31;124(30):8876-83.

PMID:
12137542
11.

The winding pathway to erythropoietin along the chemistry-biology frontier: a success at last.

Wilson RM, Dong S, Wang P, Danishefsky SJ.

Angew Chem Int Ed Engl. 2013 Jul 22;52(30):7646-65. doi: 10.1002/anie.201301666. Epub 2013 Jun 17. Review.

12.

Development of orthogonally protected hypusine for solid-phase peptide synthesis.

Song A, Tom J, Yu Z, Pham V, Tan D, Zhang D, Fang G, Yu T, Deshayes K.

J Org Chem. 2015 Apr 3;80(7):3677-81. doi: 10.1021/acs.joc.5b00110. Epub 2015 Mar 24.

PMID:
25769022
13.

Rapid total synthesis of DARPin pE59 and barnase.

Mong SK, Vinogradov AA, Simon MD, Pentelute BL.

Chembiochem. 2014 Mar 21;15(5):721-33. doi: 10.1002/cbic.201300797. Epub 2014 Mar 11.

14.

Mapping tertiary interactions in protein folding reactions: a novel mass spectrometry- and chemical synthesis-based approach.

Moss JA, Silinski P, Fitzgerald MC.

Fresenius J Anal Chem. 2001 Feb;369(3-4):252-7.

PMID:
11293701
16.

Optimisation of chemical protein cleavage for erythropoietin semi-synthesis using native chemical ligation.

Richardson JP, Macmillan D.

Org Biomol Chem. 2008 Nov 7;6(21):3977-82. doi: 10.1039/b811501j. Epub 2008 Sep 5.

18.

Effects of a polar amino acid substitution on helix formation and aggregate size along the detergent-induced peptide folding pathway.

Alvares RD, Tulumello DV, Macdonald PM, Deber CM, Prosser RS.

Biochim Biophys Acta. 2013 Feb;1828(2):373-81. doi: 10.1016/j.bbamem.2012.09.024. Epub 2012 Sep 29.

19.

Synthesis and folding of native collagen III model peptides.

Henkel W, Vogl T, Echner H, Voelter W, Urbanke C, Schleuder D, Rauterberg J.

Biochemistry. 1999 Oct 12;38(41):13610-22.

PMID:
10521268
20.

A universal strategy for preparing protected C-terminal peptides on the solid phase through an intramolecular click chemistry-based handle.

Góngora-Benítez M, Cristau M, Giraud M, Tulla-Puche J, Albericio F.

Chem Commun (Camb). 2012 Feb 25;48(17):2313-5. doi: 10.1039/c2cc17222d. Epub 2012 Jan 19.

PMID:
22262473

Supplemental Content

Support Center