N-Terminal Proline Editing for the Synthesis of Peptides with Mercaptoproline and Selenoproline: Mechanistic Insights Lead to Greater Efficiency in Proline Native Chemical Ligation-Reference-Cited by-同舟云学术

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N-Terminal Proline Editing for the Synthesis of Peptides with Mercaptoproline and Selenoproline: Mechanistic Insights Lead to Greater Efficiency in Proline Native Chemical Ligation

Published:2024-02-07 Issue:2 Volume:19 Page:536-550
ISSN:1554-8929
Container-title:ACS Chemical Biology
language:en
Short-container-title:ACS Chem. Biol.

Author:

Ludwig Brice A.¹,Forbes Christina R.¹^ORCID,Zondlo Neal J.¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716, United States

Funder

Division of Chemistry

Division of Molecular and Cellular Biosciences

U.S. Department of Defense

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acschembio.3c00705

Reference94 articles.

1. Synthesis of Proteins by Native Chemical Ligation

2. Expressed protein ligation: A general method for protein engineering

3. Total chemical synthesis of proteins

4. Recent extensions to native chemical ligation for the chemical synthesis of peptides and proteins

5. Expanding the chemical toolbox for the synthesis of large and uniquely modified proteins

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pauli Exclusion by n→π* Interactions: Implications for Paleobiology;ACS Central Science;2024-09-04

2. Proline Analogues;Chemical Reviews;2024-06-28

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