Liquid-cell transmission electron microscopy for imaging of thermosensitive recombinant polymers

被引:7
作者
Isaacson, Kyle J. [1 ,2 ]
Van Devener, Brian R. [3 ]
Steinhauff, Douglas B. [1 ,2 ]
Jensen, M. Martin [1 ,2 ]
Cappello, Joseph [4 ]
Ghandehari, Hamidreza [1 ,2 ,4 ]
机构
[1] Univ Utah, Utah Ctr Nanomed, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Biomed Engn, Salt Lake City, UT 84112 USA
[3] Univ Utah, Utah Nanofab Nano Scale Imaging & Surface Anal La, Salt Lake City, UT 84112 USA
[4] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
关键词
Elastinlike polypeptide; Recombinant protein; Polymer; Liquid-cell transmission electron microscopy; Silk-elastinlike protein; Temperature-sensitive polymer; CRITICAL SOLUTION TEMPERATURE; PROTEIN POLYMER; LCST BEHAVIOR; DYNAMICS;
D O I
10.1016/j.jconrel.2022.02.019
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Various polymers used in controlled release applications exhibit solution-based thermal responses. Unfortunately, very few characterization and imaging techniques permit resolution of individual polymers during their thermally-triggered phase transitions. Here, we demonstrate the use of temperature-ramp liquid-cell transmission electron microscopy (LCTEM) for real-time evaluation of the solution and interfacial behavior of elastinlike polypeptides (ELPs) and their self-assembled nanostructures over a temperature range incorporating their intrinsic lower critical solution temperatures (LCSTs). Individual polymers and supramolecular assemblies were discriminated dependent upon solubility states. The recombinant polymers were shown to adsorb to the silicon nitride chip window from the buffered saline solution and desorb in a temperature-dependent manner. Silkelastinlike protein block copolymers (SELPs) (composed of repeat peptide motifs of silk and elastin) differed from ELPs in thermal behavior. While both polymers were shown to cluster, only SELPs formed robust amyloidlike fibers upon heating.
引用
收藏
页码:39 / 49
页数:11
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