优化类肽合成的现场指南

IF 4.7 Q1 POLYMER SCIENCE
Abigail Mae Clapperton, Jon Babi and Helen Tran*, 
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引用次数: 6

摘要

n -取代甘氨酸(类肽)是一类拟肽分子,被用作健康、环境和药物递送材料。自动化固相合成是制备多肽最广泛使用的方法,有一系列已发表的方案和对选定合成靶点的修改。同时,新兴的溶液相合成被用来克服固相合成的局限性,获得高分子量的多肽。本展望旨在概述固相和溶液相合成的优化策略,为机器人合成器提供技术考虑,并对合成方法的进展进行展望。固相合成部分探讨了协议优化,访问复杂侧链和适应机器人合成器的步骤;溶液相合成的部分涵盖了引发剂的选择,侧链相容性,以及控制聚合效率和规模的策略。本文作为一个“现场指南”的研究人员旨在利用灵活性和适应性的肽类在他们的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Field Guide to Optimizing Peptoid Synthesis

A Field Guide to Optimizing Peptoid Synthesis

N-Substituted glycines (peptoids) are a class of peptidomimetic molecules used as materials for health, environmental, and drug delivery applications. Automated solid-phase synthesis is the most widely used approach for preparing polypeptoids, with a range of published protocols and modifications for selected synthetic targets. Simultaneously, emerging solution-phase syntheses are being leveraged to overcome limitations in solid-phase synthesis and access high-molecular weight polypeptoids. This Perspective aims to outline strategies for the optimization of both solid- and solution-phase synthesis, provide technical considerations for robotic synthesizers, and offer an outlook on advances in synthetic methodologies. The solid-phase synthesis sections explore steps for protocol optimization, accessing complex side chains, and adaptation to robotic synthesizers; the sections on solution-phase synthesis cover the selection of initiators, side chain compatibility, and strategies for controlling polymerization efficiency and scale. This text acts as a “field guide” for researchers aiming to leverage the flexibility and adaptability of peptoids in their research.

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