Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Backbone N-methylation is a pivotal peptide modification that enhances lipophilicity, metabolic stability, and binding affinity or specificity, thereby improving bioactive peptides' bioavailability. Substitution of a backbone amide hydrogen with a methyl group is a three-step procedure which is fully integrated with solid-phase peptide synthesis strategy and usually takes about 4 h. We have revolutionized this process by optimizing the method and slashing the total N-methylation procedure time from 4 h to just 40 min. Moreover, we demonstrate that N-methylation can be equally efficient regardless of the laboratory equipment used, such as a standard laboratory shaker, microwave synthesizer, or common ultrasonic bath. Our study not only results in acceleration of the N-methylation process during solid-phase peptide synthesis but also offers a flexible choice of laboratory equipment, making peptide modifications more efficient and achievable.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12150311PMC
http://dx.doi.org/10.1021/acs.joc.5c00083DOI Listing

Publication Analysis

Top Keywords

solid-phase peptide
8
peptide synthesis
8
laboratory equipment
8
time-reduced n-methylation
4
n-methylation exploring
4
exploring faster
4
faster synthesis
4
synthesis technique
4
technique backbone
4
n-methylation
4

Similar Publications

Hydrophobic Tag-Assisted Liquid-Phase Synthesis of Tirzepatide.

Org Lett

September 2025

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

The synthesis of tirzepatide relies heavily on solid phase peptide synthesis (SPPS), a process that is both costly and time-consuming. In this paper, a novel soluble liquid-phase assisted (LPPS) strategy for the efficient synthesis of tirzepatide is presented. The efficacy of the method is based on the distinct solubility properties of the soluble tag, which enables high yield synthesis while significantly reducing wastage of amino acids and solvents.

View Article and Find Full Text PDF

Incorporating non-natural amino acids (NNAAs) into peptides enhances therapeutic properties, including binding affinity, metabolic stability, and half-life time. The pursuit of novel NNAAs for improved peptide designs faces the challenge of effective synthesis of these building blocks as well as the entire peptide itself. Solid-Phase Peptide Synthesis (SPPS) is an essential technology for the automated assembly of peptides with NNAAs, necessitating careful protection for effective coupling of amino acids in the peptide chain.

View Article and Find Full Text PDF

Photocatalytic C-X Bond Cleavage Facilitates Peptide Synthesis.

J Am Chem Soc

September 2025

Center for Chemical Glycobiology, Shanghai Key Laboratory for Antibody-Drug Conjugates with Innovative Target, State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.

The ability to selectively cleave C-heteroatom bonds is critically important in chemical science, from peptide and protein synthesis to biomolecule manipulation. For example, C-heteroatom bond cleavage is widely used in fluorenylmethyloxycarbonyl/-butyl (Fmoc/Bu)-based solid-phase peptide synthesis (SPPS). Despite its usefulness, it has inextricable limitations, such as issues with hydrophobicity and side reactions, owing to the need for the use of a strong trifluoroacetic acid (TFA, a pervasive forever chemical) as the cleavage reagent.

View Article and Find Full Text PDF

Lithobates palmipes is a frog species whose skin secretions contain peptides belonging to the ranatuerin, brevinin, and temporin families. In this study, the peptide ranatuerin-2PMe was isolated and evaluated for its antimicrobial, hemolytic, antiproliferative, and chemotactic activities. Ranatuerin-2PMe (2933.

View Article and Find Full Text PDF