Rapid Flow-Based Peptide Synthesis

Patrick L. Heider(Massachusetts Institute of Technology), Andrea Adamo(Massachusetts Institute of Technology), Alexander A. Vinogradov(Massachusetts Institute of Technology), Xiyuan Li(Massachusetts Institute of Technology), Tatiana Berger(Massachusetts Institute of Technology), Rocco L. Policarpo(Massachusetts Institute of Technology), Chi Zhang(Massachusetts Institute of Technology), Yekui Zou(Massachusetts Institute of Technology), Xiaoli Liao(Massachusetts Institute of Technology), Alexander M. Spokoyny(Massachusetts Institute of Technology), Klavs F. Jensen(Massachusetts Institute of Technology), Bradley L. Pentelute(Massachusetts Institute of Technology), Mark D. Simon(Massachusetts Institute of Technology), Surin K. Mong(Massachusetts Institute of Technology)
DSpace@MIT (Massachusetts Institute of Technology)
December 1, 2013
Cited by 177Open Access
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Abstract

A flow-based solid-phase peptide synthesis methodology that enables the incorporation of an amino acid residue every 1.8 min under automatic control or every 3 min under manual control is described. This is accomplished by passing a stream of reagent through a heat exchanger into a low volume, low backpressure reaction vessel, and through a UV detector. These features enable continuous delivery of heated solvents and reagents to the solid support at high flow rate, thereby maintaining maximal concentration of reagents in the reaction vessel, quickly exchanging reagents, and eliminating the need to rapidly heat reagents after they have been added to the vessel. The UV detector enables continuous monitoring of the process. To demonstrate the broad applicability and reliability of this method, it was employed in the total synthesis of a small protein, as well as dozens of peptides. The quality of the material obtained with this method is comparable to that for traditional batch methods, and, in all cases, the desired material was readily purifiable by RP-HPLC. The application of this method to the synthesis of the 113-residue Bacillus amyloliquefaciens RNase and the 130-residue DARPin pE59 is described in the accompanying manuscript.


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