Evaluation of Efficient Non-reducing Enzymatic and Chemical Ligation Strategies for Complex Disulfide-Rich Peptides-Reference-Cited by-同舟云学术

Evaluation of Efficient Non-reducing Enzymatic and Chemical Ligation Strategies for Complex Disulfide-Rich Peptides

Published:2021-11-09 Issue:11 Volume:32 Page:2407-2419
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Tran Hue N. T.¹^ORCID,Tran Poanna¹,Deuis Jennifer R.¹,McMahon Kirsten L.¹,Yap Kuok¹^ORCID,Craik David J.¹^ORCID,Vetter Irina¹²^ORCID,Schroeder Christina I.¹³^ORCID

Affiliation:

1. Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland 4072, Australia

2. School of Pharmacy, The University of Queensland, Woolloongabba, Queensland 4102, Australia

3. Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States

Funder

National Health and Medical Research Council

Australian Research Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.bioconjchem.1c00452

Reference74 articles.

1. A Bivalent Tarantula Toxin Activates the Capsaicin Receptor, TRPV1, by Targeting the Outer Pore Domain

2. Potent neuroprotection after stroke afforded by a double-knot spider-venom peptide that inhibits acid-sensing ion channel 1a

3. Novel Class of Spider Toxin

4. TRPV1 structures in nanodiscs reveal mechanisms of ligand and lipid action

5. Structural insights into the mechanism of activation of the TRPV1 channel by a membrane-bound tarantula toxin

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