Optical biosensors based on Surface Plasmon Resonance (SPR), such as the BiacoreTM X100, are widely used to study in real-time and in label-free mode bio-molecular interactions, including those allowing the identification of single point mutations responsible of genetic diseases, such as thalassemia and cystic fibrosis. The aim of this study was to verify whether the BiacoreTM X100 can be proposed for the real-time detection of four mutations of the human gamma-globin gene causing beta-thalassemia, a genetic blood disorder associated with absence (beta0) or reduction (beta+) of adult hemoglobin and severe anemia. In particular we analyzed the most frequent thalassemia point mutations present in the Mediterranean area (beta039, beta0IVSI-1, beta+IVSI-110 and beta+IVSI-6) using a novel SPR-based interaction format where two oligonucleotide probes (one complementary to the normal sequence and the other to the mutated one) were immobilized on sensor chips and asymmetric PCR targets obtained from genomic DNA of analyzed subjects were injected. For the development of the diagnostic approach, genomic DNAs of different genotypes for each mutation were obtained from blood samples or salivary swabs of 71 subjects, including healthy individuals, heterozygous β-thalassemia carriers and homozygous β-thalassemia patients. The results obtained allow proposing a new non-invasive diagnostic SPR-based protocol for thalassemia single point mutations using blood samples and salivary swabs as a source of genomic DNA.

A novel and efficient protocol for Surface Plasmon Resonance based detection of four β-thalassemia point mutations in blood samples and salivary swabs

Breveglieri, Giulia
Primo
Investigation
;
D'Aversa, Elisabetta
Secondo
Methodology
;
Gallo, Tiziana Eleonora
Methodology
;
Pellegatti, Patrizia
Resources
;
Guerra, Giovanni
Resources
;
Cosenza, Lucia Carmela
Methodology
;
Finotti, Alessia
Membro del Collaboration Group
;
Gambari, Roberto
Penultimo
Writing – Review & Editing
;
Borgatti, Monica
Ultimo
Writing – Original Draft Preparation
2018

Abstract

Optical biosensors based on Surface Plasmon Resonance (SPR), such as the BiacoreTM X100, are widely used to study in real-time and in label-free mode bio-molecular interactions, including those allowing the identification of single point mutations responsible of genetic diseases, such as thalassemia and cystic fibrosis. The aim of this study was to verify whether the BiacoreTM X100 can be proposed for the real-time detection of four mutations of the human gamma-globin gene causing beta-thalassemia, a genetic blood disorder associated with absence (beta0) or reduction (beta+) of adult hemoglobin and severe anemia. In particular we analyzed the most frequent thalassemia point mutations present in the Mediterranean area (beta039, beta0IVSI-1, beta+IVSI-110 and beta+IVSI-6) using a novel SPR-based interaction format where two oligonucleotide probes (one complementary to the normal sequence and the other to the mutated one) were immobilized on sensor chips and asymmetric PCR targets obtained from genomic DNA of analyzed subjects were injected. For the development of the diagnostic approach, genomic DNAs of different genotypes for each mutation were obtained from blood samples or salivary swabs of 71 subjects, including healthy individuals, heterozygous β-thalassemia carriers and homozygous β-thalassemia patients. The results obtained allow proposing a new non-invasive diagnostic SPR-based protocol for thalassemia single point mutations using blood samples and salivary swabs as a source of genomic DNA.
Breveglieri, Giulia; D'Aversa, Elisabetta; Gallo, Tiziana Eleonora; Pellegatti, Patrizia; Guerra, Giovanni; Cosenza, Lucia Carmela; Finotti, Alessia; Gambari, Roberto; Borgatti, Monica
File in questo prodotto:
File Dimensione Formato  
SENSORS AND ACTUATORS B.pdf

solo gestori archivio

Tipologia: Full text (versione editoriale)
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 1.4 MB
Formato Adobe PDF
1.4 MB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/2381878
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 8
  • ???jsp.display-item.citation.isi??? 8
social impact