Supported ionic liquid materials for L-asparaginase bioconjugation
Main Author: | |
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Publication Date: | 2021 |
Other Authors: | , , , , |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10773/32915 |
Summary: | Since the average life expectancy is increasing, several fatal diseases usually related to aging, such as cancer, heart and neurological diseases have become predominant. Biopharmaceuticals, namely nucleic-acid-based products, antibodies, recombinant proteins and enzymes are fundamental to overcome these age-related diseases. Actually, the gold standard enzyme for the treatment of acute chronic lymphoblastic leukemia (ALL) is L-asparaginase (ASNase). Hence, the reusability of this high-priced drug enables the cost reduction of treatments, which allows its routinely use by a widespread population. In this work, functionalized nanomaterials, namely supported ionic liquid materials (SILs) based on silica, formerly described in the literature for the separation of natural compounds from vegetable biomass, were studied as a cost effective support for ASNase immobilization and reuse. Commercial ASNase was used for preliminary tests. Several experimental immobilization conditions, such as pH, contact time, ASNase concentration and SILs recyclability were assessed and optimized, regarding the immobilized ASNase activity, assessed by Nessler reaction, which quantifies the amount of ammonium released after the enzymatic reaction with L-asparagine and immobilization yield. In fact, ASNase immobilization onto the SILs was successfully achieved with an immobilized ASNase activity ranging from 0.6 to 0.9 U of enzyme per mg of SILs under the optimum immobilization conditions. Moreover, all SILs allowed 5 cycles of reaction, while keeping more than 75% of initial ASNase activity. Through the envisioned immobilization strategy, process costs will be considerably reduced, which can lead to a wider use of ASNase in diverse fields of application. |
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Supported ionic liquid materials for L-asparaginase bioconjugationL-asparaginaseBioconjugationSupported ionic liquid materialsSince the average life expectancy is increasing, several fatal diseases usually related to aging, such as cancer, heart and neurological diseases have become predominant. Biopharmaceuticals, namely nucleic-acid-based products, antibodies, recombinant proteins and enzymes are fundamental to overcome these age-related diseases. Actually, the gold standard enzyme for the treatment of acute chronic lymphoblastic leukemia (ALL) is L-asparaginase (ASNase). Hence, the reusability of this high-priced drug enables the cost reduction of treatments, which allows its routinely use by a widespread population. In this work, functionalized nanomaterials, namely supported ionic liquid materials (SILs) based on silica, formerly described in the literature for the separation of natural compounds from vegetable biomass, were studied as a cost effective support for ASNase immobilization and reuse. Commercial ASNase was used for preliminary tests. Several experimental immobilization conditions, such as pH, contact time, ASNase concentration and SILs recyclability were assessed and optimized, regarding the immobilized ASNase activity, assessed by Nessler reaction, which quantifies the amount of ammonium released after the enzymatic reaction with L-asparagine and immobilization yield. In fact, ASNase immobilization onto the SILs was successfully achieved with an immobilized ASNase activity ranging from 0.6 to 0.9 U of enzyme per mg of SILs under the optimum immobilization conditions. Moreover, all SILs allowed 5 cycles of reaction, while keeping more than 75% of initial ASNase activity. Through the envisioned immobilization strategy, process costs will be considerably reduced, which can lead to a wider use of ASNase in diverse fields of application.Sociedade Portuguesa de Química2022-01-13T13:07:00Z2021-07-01T00:00:00Z2021-07conference objectinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10773/32915engNunes, João C. F.Almeida, Mafalda R.Santos-Ebinuma, Valéria C.Neves, Márcia C.Freire, Mara G.Tavares, Ana P. M.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-06T04:34:59Zoai:ria.ua.pt:10773/32915Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T14:13:14.628586Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Supported ionic liquid materials for L-asparaginase bioconjugation |
title |
Supported ionic liquid materials for L-asparaginase bioconjugation |
spellingShingle |
Supported ionic liquid materials for L-asparaginase bioconjugation Nunes, João C. F. L-asparaginase Bioconjugation Supported ionic liquid materials |
title_short |
Supported ionic liquid materials for L-asparaginase bioconjugation |
title_full |
Supported ionic liquid materials for L-asparaginase bioconjugation |
title_fullStr |
Supported ionic liquid materials for L-asparaginase bioconjugation |
title_full_unstemmed |
Supported ionic liquid materials for L-asparaginase bioconjugation |
title_sort |
Supported ionic liquid materials for L-asparaginase bioconjugation |
author |
Nunes, João C. F. |
author_facet |
Nunes, João C. F. Almeida, Mafalda R. Santos-Ebinuma, Valéria C. Neves, Márcia C. Freire, Mara G. Tavares, Ana P. M. |
author_role |
author |
author2 |
Almeida, Mafalda R. Santos-Ebinuma, Valéria C. Neves, Márcia C. Freire, Mara G. Tavares, Ana P. M. |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Nunes, João C. F. Almeida, Mafalda R. Santos-Ebinuma, Valéria C. Neves, Márcia C. Freire, Mara G. Tavares, Ana P. M. |
dc.subject.por.fl_str_mv |
L-asparaginase Bioconjugation Supported ionic liquid materials |
topic |
L-asparaginase Bioconjugation Supported ionic liquid materials |
description |
Since the average life expectancy is increasing, several fatal diseases usually related to aging, such as cancer, heart and neurological diseases have become predominant. Biopharmaceuticals, namely nucleic-acid-based products, antibodies, recombinant proteins and enzymes are fundamental to overcome these age-related diseases. Actually, the gold standard enzyme for the treatment of acute chronic lymphoblastic leukemia (ALL) is L-asparaginase (ASNase). Hence, the reusability of this high-priced drug enables the cost reduction of treatments, which allows its routinely use by a widespread population. In this work, functionalized nanomaterials, namely supported ionic liquid materials (SILs) based on silica, formerly described in the literature for the separation of natural compounds from vegetable biomass, were studied as a cost effective support for ASNase immobilization and reuse. Commercial ASNase was used for preliminary tests. Several experimental immobilization conditions, such as pH, contact time, ASNase concentration and SILs recyclability were assessed and optimized, regarding the immobilized ASNase activity, assessed by Nessler reaction, which quantifies the amount of ammonium released after the enzymatic reaction with L-asparagine and immobilization yield. In fact, ASNase immobilization onto the SILs was successfully achieved with an immobilized ASNase activity ranging from 0.6 to 0.9 U of enzyme per mg of SILs under the optimum immobilization conditions. Moreover, all SILs allowed 5 cycles of reaction, while keeping more than 75% of initial ASNase activity. Through the envisioned immobilization strategy, process costs will be considerably reduced, which can lead to a wider use of ASNase in diverse fields of application. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-07-01T00:00:00Z 2021-07 2022-01-13T13:07:00Z |
dc.type.driver.fl_str_mv |
conference object |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10773/32915 |
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http://hdl.handle.net/10773/32915 |
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eng |
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eng |
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application/pdf |
dc.publisher.none.fl_str_mv |
Sociedade Portuguesa de Química |
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Sociedade Portuguesa de Química |
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