Facile Cu(ii)-mediated conjugation of thioesters and thioacids to peptides and proteins under mild conditions-Reference-Cited by-同舟云学术

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Facile Cu(ii)-mediated conjugation of thioesters and thioacids to peptides and proteins under mild conditions

Published:2018 Issue:19 Volume:16 Page:3610-3614
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Sun Yao¹²³⁴⁵^ORCID,Lyu Zhenbin⁶⁷⁸⁹¹⁰,Wang Zhiqiang⁶⁷⁸⁹¹⁰,Zeng Xiaodong⁶⁷⁸⁹¹⁰,Zhou Hui⁶⁷⁸⁹¹⁰^ORCID,Xu Fuchun¹¹¹²¹³¹⁰,Chen Ziyang⁶⁷⁸⁹¹⁰,Xu Yuling¹²³⁴⁵,Xu Ping¹⁴¹⁵¹⁶¹⁷¹⁰,Hong Xuechuan⁶⁷⁸⁹¹⁰^ORCID

Affiliation:

1. Key Laboratory of Pesticides and Chemical Biology

2. Ministry of Education

3. Hubei International Scientific and Technological Cooperation Base of Pesticide and Green Synthesis

4. Chemical Biology Center

5. College of Chemistry

6. State Key Laboratory of Virology

7. Zhongnan Hospital of Wuhan University

8. Wuhan University School of Pharmaceutical Sciences

9. Wuhan 430071

10. China

11. Medical College

12. Tibet University

13. Lasa

14. State Key Laboratory of Proteomics

15. National Center for Protein Sciences Beijing

16. Beijing Institute of Radiation Medicine

17. Beijing 102206

Abstract

The bioconjugation of peptide derivatives such as polypeptides, peptide-based probes and proteins is a vibrant area in many scientific fields.

Funder

National Natural Science Foundation of China

Ministry of Education of the People's Republic of China

Central China Normal University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB00536B

Reference37 articles.

1. One-step site-specific modification of native proteins with 2-pyridinecarboxyaldehydes

2. Development of New Thioester Equivalents for Protein Chemical Synthesis

3. Bioconjugation – using selective chemistry to enhance the properties of proteins and peptides as therapeutics and carriers

4. UPAR targeted molecular imaging of cancers with small molecule-based probes

5. Bioorthogonal cyclization-mediated in situ self-assembly of small-molecule probes for imaging caspase activity in vivo

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