Optimal Biofunctionalization of Gold Nanoislands for Electrochemical Detection of Soluble Programmed Death Ligand 1

Soluble programmed death ligand‐1 (sPD‐L1), a pivotal immune checkpoint protein, serves as a biomarker for evaluating the efficacy of cancer therapies. Aptamers, as highly stable and specific recognition elements, play an essential role in emerging point‐of‐care diagnostic technologies. Yet, crucial...

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Main Authors: Zahra Lotfibakalani, Borui Liu, Monalisha Ghosh Dastidar, Thành Trân‐Phú, Krishnan Murugappan, Parisa Moazzam, David R Nisbet, Antonio Tricoli
Format: Article
Language:English
Published: Wiley-VCH 2025-01-01
Series:Small Science
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Online Access:https://doi.org/10.1002/smsc.202400411
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author Zahra Lotfibakalani
Borui Liu
Monalisha Ghosh Dastidar
Thành Trân‐Phú
Krishnan Murugappan
Parisa Moazzam
David R Nisbet
Antonio Tricoli
author_facet Zahra Lotfibakalani
Borui Liu
Monalisha Ghosh Dastidar
Thành Trân‐Phú
Krishnan Murugappan
Parisa Moazzam
David R Nisbet
Antonio Tricoli
author_sort Zahra Lotfibakalani
collection DOAJ
description Soluble programmed death ligand‐1 (sPD‐L1), a pivotal immune checkpoint protein, serves as a biomarker for evaluating the efficacy of cancer therapies. Aptamers, as highly stable and specific recognition elements, play an essential role in emerging point‐of‐care diagnostic technologies. Yet, crucial advancements rely on engineering the intricate interaction between aptamers and sensor substrates to achieve specificity and signal enhancement. Here, a comprehensive physicochemical characterization and performance optimization of a sPD‐L1 aptamer‐based biosensor by a complementary set of state‐of‐the‐art methodologies is presented, including atomic force microscopy‐based infrared spectroscopy and high‐resolution transmission electron microscopy, providing critical insights on the surface coverage and binding mechanism. The optimal nanoaptasensors detect sPD‐L1 across a wide concentration range (from am to μm) with a detection limit of 0.76 am in both buffer and mouse serum samples. These findings, demonstrating superior selectivity, reproducibility, and stability, pave the way for engineering miniaturized point‐of‐care and portable biosensors for cancer diagnostics.
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spelling doaj-art-ebf5eb143cc743b48b8322d6ca4b36b62025-08-20T02:39:58ZengWiley-VCHSmall Science2688-40462025-01-0151n/an/a10.1002/smsc.202400411Optimal Biofunctionalization of Gold Nanoislands for Electrochemical Detection of Soluble Programmed Death Ligand 1Zahra Lotfibakalani0Borui Liu1Monalisha Ghosh Dastidar2Thành Trân‐Phú3Krishnan Murugappan4Parisa Moazzam5David R Nisbet6Antonio Tricoli7Nanotechnology Research Laboratory Faculty of Engineering The University of Sydney Darlington NSW 2008 AustraliaNanotechnology Research Laboratory Faculty of Engineering The University of Sydney Darlington NSW 2008 AustraliaNanotechnology Research Laboratory Research School of Chemistry Australian National University Canberra ACT 2601 AustraliaNanotechnology Research Laboratory Research School of Chemistry Australian National University Canberra ACT 2601 AustraliaNanotechnology Research Laboratory Research School of Chemistry Australian National University Canberra ACT 2601 AustraliaNanotechnology Research Laboratory Faculty of Engineering The University of Sydney Darlington NSW 2008 AustraliaThe Graeme Clark Institute The University of Melbourne Melbourne VIC 3010 AustraliaNanotechnology Research Laboratory Faculty of Engineering The University of Sydney Darlington NSW 2008 AustraliaSoluble programmed death ligand‐1 (sPD‐L1), a pivotal immune checkpoint protein, serves as a biomarker for evaluating the efficacy of cancer therapies. Aptamers, as highly stable and specific recognition elements, play an essential role in emerging point‐of‐care diagnostic technologies. Yet, crucial advancements rely on engineering the intricate interaction between aptamers and sensor substrates to achieve specificity and signal enhancement. Here, a comprehensive physicochemical characterization and performance optimization of a sPD‐L1 aptamer‐based biosensor by a complementary set of state‐of‐the‐art methodologies is presented, including atomic force microscopy‐based infrared spectroscopy and high‐resolution transmission electron microscopy, providing critical insights on the surface coverage and binding mechanism. The optimal nanoaptasensors detect sPD‐L1 across a wide concentration range (from am to μm) with a detection limit of 0.76 am in both buffer and mouse serum samples. These findings, demonstrating superior selectivity, reproducibility, and stability, pave the way for engineering miniaturized point‐of‐care and portable biosensors for cancer diagnostics.https://doi.org/10.1002/smsc.202400411aptasensorselectrochemical detectionsgold nanoislandspoint‐of‐care biosensorssoluble programmed death ligand‐1
spellingShingle Zahra Lotfibakalani
Borui Liu
Monalisha Ghosh Dastidar
Thành Trân‐Phú
Krishnan Murugappan
Parisa Moazzam
David R Nisbet
Antonio Tricoli
Optimal Biofunctionalization of Gold Nanoislands for Electrochemical Detection of Soluble Programmed Death Ligand 1
Small Science
aptasensors
electrochemical detections
gold nanoislands
point‐of‐care biosensors
soluble programmed death ligand‐1
title Optimal Biofunctionalization of Gold Nanoislands for Electrochemical Detection of Soluble Programmed Death Ligand 1
title_full Optimal Biofunctionalization of Gold Nanoislands for Electrochemical Detection of Soluble Programmed Death Ligand 1
title_fullStr Optimal Biofunctionalization of Gold Nanoislands for Electrochemical Detection of Soluble Programmed Death Ligand 1
title_full_unstemmed Optimal Biofunctionalization of Gold Nanoislands for Electrochemical Detection of Soluble Programmed Death Ligand 1
title_short Optimal Biofunctionalization of Gold Nanoislands for Electrochemical Detection of Soluble Programmed Death Ligand 1
title_sort optimal biofunctionalization of gold nanoislands for electrochemical detection of soluble programmed death ligand 1
topic aptasensors
electrochemical detections
gold nanoislands
point‐of‐care biosensors
soluble programmed death ligand‐1
url https://doi.org/10.1002/smsc.202400411
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