Unknown

Dataset Information

0

Novel Nanozeolitic Imidazolate Framework (ZIF-8)-Luciferase Biocomposite for Nanosensing Applications.


ABSTRACT: The identification of new strategies to improve the stability of proteins is of utmost importance for a number of applications, from biosensing to biocatalysis. Metal-organic frameworks (MOFs) have been shown as a versatile host platform for the immobilization of proteins, with the potential to protect proteins in harsh conditions. In this work, a new thermostable luciferase mutant has been selected as a bioluminescent protein model to investigate the suitability of MOFs to improve its stability and prompt its applications in real-world applications, for example, ATP detection in portable systems. The luciferase has been immobilized onto zeolitic imidazolate framework-8 (ZIF-8) to obtain a bioluminescent biocomposite with enhanced performance. The biocomposite ZIF-8@luc has been characterized in harsh conditions (e.g., high temperature, non-native pH, etc.). Bioluminescence properties confirmed that MOF enhanced the luciferase stability at acidic pH, in the presence of organic solvents, and at -20 °C. To assess the feasibility of this approach, the recyclability, storage stability, precision, and Michaelis-Menten constants (Km) for ATP and d-luciferin have been also evaluated. As a proof of principle, the suitability for ATP detection was investigated and the biocomposite outperformed the free enzyme in the same experimental conditions, achieving a limit of detection for ATP down to 0.2 fmol.

SUBMITTER: Martinez-Perez-Cejuela H 

PROVIDER: S-EPMC9893222 | biostudies-literature | 2023 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Novel Nanozeolitic Imidazolate Framework (ZIF-8)-Luciferase Biocomposite for Nanosensing Applications.

Martínez-Pérez-Cejuela Héctor H   Gregucci Denise D   Calabretta Maria Maddalena MM   Simó-Alfonso Ernesto Francisco EF   Herrero-Martínez José Manuel JM   Michelini Elisa E  

Analytical chemistry 20221206 4


The identification of new strategies to improve the stability of proteins is of utmost importance for a number of applications, from biosensing to biocatalysis. Metal-organic frameworks (MOFs) have been shown as a versatile host platform for the immobilization of proteins, with the potential to protect proteins in harsh conditions. In this work, a new thermostable luciferase mutant has been selected as a bioluminescent protein model to investigate the suitability of MOFs to improve its stability  ...[more]

Similar Datasets

| S-EPMC4736437 | biostudies-literature
| S-EPMC8362128 | biostudies-literature
| S-EPMC6088371 | biostudies-literature
| S-EPMC8730619 | biostudies-literature
| S-EPMC9030954 | biostudies-literature
| S-EPMC9458003 | biostudies-literature
| S-EPMC10532010 | biostudies-literature
| S-EPMC8159372 | biostudies-literature
| S-EPMC5907525 | biostudies-literature
| S-EPMC8655944 | biostudies-literature