Boosting the in situ encapsulation of proteins with MIL-100(Fe): the role of strong Lewis acid centers

09 November 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Encapsulation of biomolecules using Metal-Organic Frameworks (MOFs) to form stable biocomposites has been demonstrated a valuable strategy for their preservation and controlled release, which has been however restricted to specific electrostatic surface conditions. We present a general in situ strategy that promotes the spontaneous MOF growth onto a broad variety of proteins, for the first time, regardless of their surface nature. We demonstrate that MOFs based on cations exhibiting considerable inherent acidity such as MIL-100(Fe) enable biomolecule encapsulation, including alkaline proteins previously inaccesible by the welldeveloped in situ encapsulation with azolate-based MOFs. In particular, MIL-100(Fe) scaffold permits effective encapsulation of proteins with very distinct surface nature, retaining their activity and allowing triggered release under biocompatible conditions. This general strategy will enable an ample use of biomolecules in desired biolotechnological applications.

Supplementary materials

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Title
Boosting the in situ encapsulation of proteins with MIL-100(Fe): the role of strong Lewis acid centers
Description
Contents S1. MATERIALS AND REAGENTS S2. SYNTHESIS OF MATERIALS S3. METHODS S4. PHYSICO-CHEMICAL CHARACTERIZATION CHARACTERIZATION OF Fe-BTC AND MIL-100(Fe) ANALYSIS OF PARTICLE SIZE FOURIER TRANSFORM INFRARED (FTIR) SPECTROSCOPY THERMOGRAVIMETRIC ANALYSIS (TGA) ELECTROSTATIC CHARACTERIZATION ENZYME RELEASE STUDIES ACTIVITY TESTS S5. BIBLIOGRAPHY
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