Application of the All-Hydrocarbon Stapling Technique in the Design of Membrane-Active Peptides

The threats of drug resistance and new emerging pathogens have led to an urgent need to develop alternative treatment therapies. Recently, considerable research efforts have focused on membrane-active peptides (MAPs), a category of peptides in drug discovery with antimicrobial, anticancer, and cell...

Mô tả chi tiết

Lưu vào:
Hiển thị chi tiết
Tác giả chính: Huy Xuan, Luong, Hai Thi Phuong, Bui, Truong, Thanh Tung
Định dạng: Bài trích
Ngôn ngữ:English
Nhà xuất bản: ACS Publications 2022
Chủ đề:
Truy cập trực tuyến:https://pubs.acs.org/doi/10.1021/acs.jmedchem.1c01744
https://dlib.phenikaa-uni.edu.vn/handle/PNK/5873
https://doi.org/10.1021/acs.jmedchem.1c01744
Từ khóa: Thêm từ khóa
Không có từ khóa, Hãy là người đầu tiên đánh dấu biểu ghi này!
Mô tả
Tóm tắt:The threats of drug resistance and new emerging pathogens have led to an urgent need to develop alternative treatment therapies. Recently, considerable research efforts have focused on membrane-active peptides (MAPs), a category of peptides in drug discovery with antimicrobial, anticancer, and cell penetration activities that have demonstrated their potential to be multifunctional agents. Nonetheless, natural MAPs have encountered various disadvantages, which mainly include poor bioavailability, the lack of a secondary structure in short peptides, and high production costs for long peptide sequences. Hence, an “all-hydrocarbon stapling system” has been applied to these peptides and proven to effectively stabilize the helical conformations, improving proteolytic resistance and increasing both the potency and the cell permeability. In this review, we summarized and categorized the advances made using this powerful technique in the development of stapled MAPs. Furthermore, outstanding issues and suggestions for future design within each subcategory were thoroughly discussed.