Research Article
Microwave-Assisted Green Solid-Phase Peptide Synthesis Using γ-Valerolactone (GVL) as Solvent
Ashish Kumar†‡, Yahya E. Jad‡, Jonathan M. Collins§, Fernando Albericio*†∥⊥ , and Beatriz G. de la Torre*#
† School of Chemistry and Physics, University of KwaZulu-Natal , University Road, Westville, Durban 4001 , South Africa
‡ Catalysis and Peptide Research Unit, School of Health Sciences, University of KwaZulu-Natal, University Road, Westville, Durban 4001 , South Africa
§ CEM Corporation, 3100 Smith Farm Road, Matthews , North Carolina 28104 , United States
∥ Department of Organic Chemistry, University of Barcelona, Martí i Franqués 1-11, Barcelona 08028 , Spain
⊥ CIBER-BBN, Networking Centre on Bioengineering, Biomaterials and Nanomedicine, Barcelona Science Park, Baldiri Reixac 10, Barcelona 08028 , Spain
# KRISP, College of Health Sciences, University of KwaZulu-Natal, Durban 4001 , South Africa
ACS Sustainable Chem. Eng., 2018, 6 (6), pp 8034–8039
DOI: 10.1021/acssuschemeng.8b01531
Publication Date (Web): April 29, 2018
Copyright © 2018 American Chemical Society
*E-mail: albericio@ukzn.ac.za., *E-mail: garciadelatorreb@ukzn.ac.za.
Synopsis
A combination of nature and technology, helping to make greener the synthesis of peptides, is reported.
Abstract
The increasing demand for synthetic peptides in various research fields raises a challenge, namely, the development of greener methods for their preparation. Here we report on an ecofriendly solid-phase peptide synthesis (SPPS) methodology. Substitution of the hazardous solvent DMF by the biomass-derived organic solvent γ-valerolactone (GVL), together with the application of microwave-assisted automated SPPS, allowed the synthesis of peptides with a wide range of lengths and high purity using polystyrene- and polyethylene-glycol-based resins. The yields achieved were comparable to those obtained with standard methodologies. To date, this is the greenest approach reported in terms of the solvent used, waste generated, and energy efficiency.
The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acssuschemeng.8b01531.
- HPLC and MS data of the synthesized peptides (PDF)
- Green Solid-Phase Peptide Synthesis (GSPPS) 3. Green Solvents for Fmoc Removal in Peptide ChemistryOrganic Process Research & DevelopmentJad, Govender, Kruger, El-Faham, de la Torre, and Albericio2017 21 (3), pp 365–369Abstract: DMF (N,N-dimethylformamide) is the most widely used solvent for Fmoc-SPPS, which is the conventional method of choice for peptide synthesis. It is usually employed for coupling, washing, and Fmoc-removal steps. We have recently reported greener solvents ...
- Green Solid-Phase Peptide Synthesis 2. 2-Methyltetrahydrofuran and Ethyl Acetate for Solid-Phase Peptide Synthesis under Green ConditionsACS Sustainable Chemistry & EngineeringJad, Acosta, Govender, Kruger, El-Faham, de la Torre, and Albericio2016 4 (12), pp 6809–6814Abstract: N,N-Dimethylformamide (DMF), N-methyl-2-pyrrolidone, and dichloromethane (DCM) are the most widely used solvents for Fmoc solid-phase peptide synthesis (SPPS). These solvents are considered hazardous chemicals and are normally used in large amounts for ...The hazardous solvents dimethylformamide and dichloromethane were substituted with greener alternatives 2-methyltetrahydrofuran and ethyl acetate for green solid-phase peptide synthesis.
- Amino Acid-Protecting GroupsChemical ReviewsIsidro-Llobet, Álvarez and Albericio2009 109 (6), pp 2455–2504
- N-Butylpyrrolidinone as Alternative Solvent for Solid-Phase Peptide SynthesisOrganic Process Research & DevelopmentLopez, Pletscher, Aemissegger, Bucher, and Gallou2018 22 (4), pp 494–503Abstract: By means of a systematic approach, several green solvent candidates were tested for their feasibility to replace the reprotoxic dimethylformamide (DMF) as a solvent used in solid-phase peptide synthesis (SPPS). According to the results presented in this ...
- Choosing the Right Coupling Reagent for Peptides: A Twenty-Five-Year JourneyOrganic Process Research & DevelopmentAlbericio, and El-Faham2018 22 (7), pp 760–772Abstract: This work is not a typical review that is trying to cover all coupling reagents in-depth. This is a personal account—it is written in the first person—seeking to summarize the 25 years of collaboration that has brought the release of several products onto ...
- Solid Phase Peptide Synthesis. I. The Synthesis of a TetrapeptideJournal of the American Chemical SocietyMerrifield1963 85 (14), pp 2149–2154
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Article Views: 204 Times
Received 4 April 2018
Published online 29 April 2018
Published in print 4 June 2018
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