成核
生物分子
傅里叶变换红外光谱
纳米材料
蛋白质结晶
圆二色性
结晶
化学
透射电子显微镜
扫描电子显微镜
荧光光谱法
材料科学
化学工程
红外光谱学
粉末衍射
结晶学
荧光
纳米技术
有机化学
工程类
物理
复合材料
量子力学
作者
Brooke P. Carpenter,A. Rain Talosig,Justin T. Mulvey,Jovany G. Merham,Jamie Esquivel,Ben Rose,Alana F. Ogata,Dmitry A. Fishman,Joseph P. Patterson
标识
DOI:10.1021/acs.chemmater.2c01903
摘要
Metal-organic frameworks (MOFs) are a class of porous nanomaterials that have been extensively studied as enzyme immobilization substrates. During in situ immobilization, MOF nucleation is driven by biomolecules with low isoelectric points. Investigation of how biomolecules control MOF self-assembly mechanisms on the molecular level is key to designing nanomaterials with desired physical and chemical properties. Here, we demonstrate how molecular modifications of bovine serum albumin (BSA) with fluorescein isothiocyanate (FITC) can affect MOF crystal size, morphology, and encapsulation efficiency. Final crystal properties are characterized using scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), fluorescent microscopy, and fluorescence spectroscopy. To probe MOF self-assembly, in situ experiments were performed using cryogenic transmission electron microscopy (cryo-TEM) and X-ray diffraction (XRD). Biophysical characterization of BSA and FITC-BSA was performed using ζ potential, mass spectrometry, circular dichroism studies, fluorescence spectroscopy, and Fourier transform infrared (FTIR) spectroscopy. The combined data reveal that protein folding and stability within amorphous precursors are contributing factors in the rate, extent, and mechanism of crystallization. Thus, our results suggest molecular modifications as promising methods for fine-tuning protein@MOFs' nucleation and growth.
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