Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139 (USA).
Chembiochem. 2014 Mar 21;15(5):713-20. doi: 10.1002/cbic.201300796. Epub 2014 Mar 11.
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.
描述了一种基于流量的固相肽合成方法,该方法可在自动控制下每 1.8 分钟或在手动控制下每 3 分钟掺入一个氨基酸残基。这是通过将试剂流通过热交换器进入小体积、低背压反应容器,并通过 UV 检测器来实现的。这些特点能够以高流速连续向固体载体输送加热的溶剂和试剂,从而保持反应容器中试剂的最大浓度,快速交换试剂,并消除在将试剂添加到容器后快速加热试剂的需要。UV 检测器能够连续监测该过程。为了证明该方法的广泛适用性和可靠性,将其用于小蛋白的全合成以及数十种肽的合成。用该方法获得的材料的质量与传统分批方法相当,并且在所有情况下,所需的材料都可以通过 RP-HPLC 轻松纯化。该方法在芽孢杆菌解淀粉芽孢杆菌 RNase 的 113 个残基和 DARPin pE59 的 130 个残基的合成中的应用在随附的手稿中进行了描述。