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A New Age for Biomedical Applications of Ribosome Inactivating Proteins (RIPs): from Bioconjugate to Nanoconstructs

Overview
Journal J Biomed Sci
Publisher Biomed Central
Specialty Biology
Date 2016 Jul 22
PMID 27439918
Citations 26
Authors
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Abstract

Ribosome-inactivating proteins (RIPs) are enzymes (3.2.2.22) that possess N-glycosilase activity that irreversibly inhibits protein synthesis. RIPs have been found in plants, fungi, algae, and bacteria; their biological role is still under investigation, even if it has been recognized their role in plant defence against predators and viruses. Nevertheless, several studies on these toxins have been performed to evaluate their applicability in the biomedical field making RIPs selectively toxic towards target cells. Indeed, these molecules are extensively used to produce chimeric biomolecules, such as immunotoxins or protein/peptides conjugates. However, to date, clinical use of most of these bioconiujates has been limited by toxicity and immunogenicity. More recently, material sciences have provided a wide range of nanomaterials to be used as excellent vehicles for toxin-delivery, since they are characterized by improved stability, solubility, and in vivo pharmacokinetics. This review discusses progresses in the development of RIPs bioconjugates, with particular attention to the recent use of nanomaterials, whose appropriate design opens up a broad range of different possibilities to the use of RIPs in novel therapeutic approaches in human diseases.

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References
1.
Tamburino R, Pizzo E, Sarcinelli C, Poerio E, Tedeschi F, Ficca A . Enhanced cytotoxic activity of a bifunctional chimeric protein containing a type 1 ribosome-inactivating protein and a serine protease inhibitor. Biochimie. 2012; 94(9):1990-6. DOI: 10.1016/j.biochi.2012.05.022. View

2.
Nielsen K, Boston R . RIBOSOME-INACTIVATING PROTEINS: A Plant Perspective. Annu Rev Plant Physiol Plant Mol Biol. 2001; 52:785-816. DOI: 10.1146/annurev.arplant.52.1.785. View

3.
Wicaksono P, Name S, Martien R, Ismail H . Formulation and Cytotoxicity of Ribosome-Inactivating Protein Mirabilis Jalapa L. Nanoparticles Using Alginate-Low Viscosity Chitosan Conjugated with Anti-Epcam Antibodies in the T47D Breast Cancer Cell Line. Asian Pac J Cancer Prev. 2016; 17(4):2277-84. DOI: 10.7314/apjcp.2016.17.4.2277. View

4.
Lyu M, Cao Y, Mohamedali K, Rosenblum M . Cell-targeting fusion constructs containing recombinant gelonin. Methods Enzymol. 2012; 502:167-214. DOI: 10.1016/B978-0-12-416039-2.00008-2. View

5.
Di Maro A, Valbonesi P, Bolognesi A, Stirpe F, De Luca P, Siniscalco Gigliano G . Isolation and characterization of four type-1 ribosome-inactivating proteins, with polynucleotide:adenosine glycosidase activity, from leaves of Phytolacca dioica L. Planta. 1999; 208(1):125-31. DOI: 10.1007/s004250050542. View