Modulation of the Translation Efficiency of Heterologous mRNA and Target Protein Stability in a Plant System: The Case Study of Interferon-αA

• Published in: Plants (Basel) Vol. 11; no. 19; p. 2450
• Main Authors: Tyurin, Alexander A, Mustafaev, Orkhan, Suhorukova, Aleksandra V, Pavlenko, Olga S, Fridman, Viktoriia A, Demyanchuk, Ilya S, Goldenkova-Pavlova, Irina V
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01-09-2022; MDPI
• Subjects: 5' Untranslated Regions; Accumulation; Amino acids; Biological activity; Case studies; Efficiency; Enzymatic activity; Enzyme activity; Ethanol; Gene expression; Genetic aspects; Genomes; Interferon; interferon-αA; Lysates; Medical research; Messenger RNA; mRNA stability; Pharmaceuticals; Physiological aspects; Plant cells; plant farming; Plants; Polypeptides; Protein purification; protein-stabilizing partner; Proteins; Proteomes; Purification; Regulatory sequences; System effectiveness; thermostable lichenase; Vaccines; Russia
• ISSN: 2223-7747; 2223-7747
• DOI: 10.3390/plants11192450

A broad and amazingly intricate network of mechanisms underlying the decoding of a plant genome into the proteome forces the researcher to design new strategies to enhance both the accumulation of recombinant proteins and their purification from plants and to improve the available relevant strategies. In this paper, we propose new approaches to optimize a codon composition of target genes (case study of interferon-αA) and to search for regulatory sequences (case study of 5′UTR), and we demonstrated their effectiveness in increasing the synthesis of recombinant proteins in plant systems. In addition, we convincingly show that the approach utilizing stabilization of the protein product according to the N-end rule or a new protein-stabilizing partner (thermostable lichenase) is sufficiently effective and results in a significant increase in the protein yield manufactured in a plant system. Moreover, it is validly demonstrated that thermostable lichenase as a protein-stabilizing partner not only has no negative effect on the target protein activity (interferon-αA) integrated in its sequence, but rather enhances the accumulation of the target protein product in plant cells. In addition, the retention of lichenase enzyme activity and interferon biological activity after the incubation of plant protein lysates at 65 °C and precipitation of nontarget proteins with ethanol is applicable to a rapid and inexpensive purification of fusion proteins, thereby confirming the utility of thermostable lichenase as a protein-stabilizing partner for plant systems.