Literature DB >> 26086408

Methods, setup and safe handling for anhydrous hydrogen fluoride cleavage in Boc solid-phase peptide synthesis.

Markus Muttenthaler1, Fernando Albericio2, Philip E Dawson3.   

Abstract

Solid-phase peptide synthesis (SPPS) using tert-butyloxycarbonyl (Boc)/benzyl (Bzl) chemistry is an indispensable technique in many laboratories around the globe, and it provides peptides to the pharmaceutical industry and to thousands of scientists working in basic research. The Boc/Bzl strategy has several advantages, including reliability in the synthesis of long and difficult polypeptides, alternative orthogonality regarding protecting groups and ease of producing C-terminal thioesters for native chemical ligation applications. In this process, anhydrous hydrogen fluoride (HF) is used to remove the side chain protecting groups of the assembled peptide and to release the peptide from the resin, a process typically described as 'HF cleavage'. This protocol describes the general methodology, apparatus setup and safe handling of HF, with the aim of providing comprehensive information on the safe use of this valuable, well-studied and validated cleavage technique. We explain the cleavage mechanism, the physicochemical properties and risks of HF, first aid measures and the correct use of the apparatus. In addition, we provide advice on scavenger selection, as well as a troubleshooting section and video material illustrating key steps of the procedure. The protocol comprises precleavage sample preparation (30 min-2.5 h), complete HF cleavage procedure (2 h) and reaction workup (30 min).

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Year:  2015        PMID: 26086408     DOI: 10.1038/nprot.2015.061

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  15 in total

1.  Click-Based Libraries of SFTI-1 Peptides: New Methods Using Reversed-Phase Silica.

Authors:  Philip A Cistrone; Philip E Dawson
Journal:  ACS Comb Sci       Date:  2016-03-03       Impact factor: 3.784

2.  Anhydrous Hydrogen Fluoride Cleavage in Boc Solid Phase Peptide Synthesis.

Authors:  Kirtikumar B Jadhav; Katrina J Woolcock; Markus Muttenthaler
Journal:  Methods Mol Biol       Date:  2020

3.  Bifluoride-catalysed sulfur(VI) fluoride exchange reaction for the synthesis of polysulfates and polysulfonates.

Authors:  Bing Gao; Linda Zhang; Qinheng Zheng; Feng Zhou; Liana M Klivansky; Jianmei Lu; Yi Liu; Jiajia Dong; Peng Wu; K Barry Sharpless
Journal:  Nat Chem       Date:  2017-06-19       Impact factor: 24.427

4.  A Facile N-Mercaptoethoxyglycinamide (MEGA) Linker Approach to Peptide Thioesterification and Cyclization.

Authors:  Patrick M M Shelton; Caroline E Weller; Champak Chatterjee
Journal:  J Am Chem Soc       Date:  2017-03-09       Impact factor: 15.419

5.  Fmoc Solid Phase Peptide Synthesis of Oxytocin and Analogues.

Authors:  Thomas Kremsmayr; Markus Muttenthaler
Journal:  Methods Mol Biol       Date:  2022

6.  Leveraging the Knorr Pyrazole Synthesis for the Facile Generation of Thioester Surrogates for use in Native Chemical Ligation.

Authors:  Dillon T Flood; Jordi C J Hintzen; Michael J Bird; Philip A Cistrone; Jason S Chen; Philip E Dawson
Journal:  Angew Chem Int Ed Engl       Date:  2018-08-10       Impact factor: 15.336

7.  On-resin strategy to label α-conotoxins: Cy5-RgIA, a potent α9α10 nicotinic acetylcholine receptor imaging probe.

Authors:  Markus Muttenthaler; Simon T Nevin; Marco Inserra; Richard J Lewis; David J Adams; Paul Alewood
Journal:  Aust J Chem       Date:  2019-12-03       Impact factor: 1.321

8.  Chemical synthesis of human trefoil factor 1 (TFF1) and its homodimer provides novel insights into their mechanisms of action.

Authors:  Nayara Braga Emidio; Hayeon Baik; David Lee; René Stürmer; Jörn Heuer; Alysha G Elliott; Mark A T Blaskovich; Katharina Haupenthal; Nicole Tegtmeyer; Werner Hoffmann; Christina I Schroeder; Markus Muttenthaler
Journal:  Chem Commun (Camb)       Date:  2020-05-11       Impact factor: 6.222

9.  Improving the Gastrointestinal Stability of Linaclotide.

Authors:  Nayara Braga Emidio; Hue N T Tran; Asa Andersson; Philip E Dawson; Fernando Albericio; Irina Vetter; Markus Muttenthaler
Journal:  J Med Chem       Date:  2021-05-12       Impact factor: 7.446

10.  Subtle modifications to oxytocin produce ligands that retain potency and improved selectivity across species.

Authors:  Markus Muttenthaler; Åsa Andersson; Irina Vetter; Rohit Menon; Marta Busnelli; Lotten Ragnarsson; Christian Bergmayr; Sarah Arrowsmith; Jennifer R Deuis; Han Sheng Chiu; Nathan J Palpant; Margaret O'Brien; Terry J Smith; Susan Wray; Inga D Neumann; Christian W Gruber; Richard J Lewis; Paul F Alewood
Journal:  Sci Signal       Date:  2017-12-05       Impact factor: 8.192

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