| Literature DB >> 19177172 |
Erik C B Johnson1, Stephen B H Kent.
Abstract
Modification of a peptide-(α)thioester with a sequence of six arginines on the thioester leaving group can render soluble all peptides derived from a polytopic integral membrane protein. This strategy greatly simplifies the synthesis of peptide-(α)thioester building blocks for the total chemical synthesis of integral membrane proteins by native chemical ligation.Entities:
Year: 2007 PMID: 19177172 PMCID: PMC2631171 DOI: 10.1016/j.tetlet.2007.01.030
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.415