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本文引用的文献

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Colorimetric logic gates for small molecules using split/integrated aptamers and unmodified gold nanoparticles.基于分裂/集成适体和未经修饰的金纳米粒子的小分子比色逻辑门。
Chem Commun (Camb). 2011 Sep 7;47(33):9435-7. doi: 10.1039/c1cc13459k. Epub 2011 Jul 21.
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Colorimetric logic gates based on supramolecular DNAzyme structures.基于超分子脱氧核酶结构的比色逻辑门。
Angew Chem Int Ed Engl. 2010 Jun 14;49(26):4438-42. doi: 10.1002/anie.201000840.
3
Platelet-derived growth factor-B normalizes micromorphology and vessel function in vascular endothelial growth factor-A-induced squamous cell carcinomas.血小板衍生生长因子-B 可使血管内皮生长因子-A 诱导的鳞状细胞癌的微观形态和血管功能正常化。
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Aptamer nano-flares for molecular detection in living cells.用于活细胞分子检测的适体纳米荧光探针。
Nano Lett. 2009 Sep;9(9):3258-61. doi: 10.1021/nl901517b.
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Easy design of logic gates based on aptazymes and noncrosslinking gold nanoparticle aggregation.基于适体酶和非交联金纳米颗粒聚集的逻辑门简易设计。
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适体-纳米颗粒组装用于基于逻辑的检测。

Aptamer-nanoparticle assembly for logic-based detection.

机构信息

Center for Research at Bio/nano Interface, Department of Chemistry and Department of Physiology and Functional Genomics, Shands Cancer Center, University of Florida , Gainesville, Florida 32611-7200, United States.

出版信息

ACS Appl Mater Interfaces. 2012 Jun 27;4(6):3007-11. doi: 10.1021/am300374q. Epub 2012 Jun 18.

DOI:10.1021/am300374q
PMID:22650355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3483412/
Abstract

In this work, gold nanoparticles perform Boolean logic operations in response to two proangiogenic targets important in cancer diagnosis and treatment: PDGF and VEGF. In the absence of protein target, gold nanoparticles are initially dispersed as a red solution; the addition of target proteins causes nanoparticle aggregation, turning the solution blue, as well as the release of dye-labeled aptamer probes, which causes an increase in fluorescence. These outputs constitute an AND or OR gate for simultaneous protein detection. We believe this logic-gate-based detection system will become the basis for novel rapid, cheap, and reliable sensors for diagnostic applications.

摘要

在这项工作中,金纳米粒子对两种在癌症诊断和治疗中非常重要的促血管生成靶点 PDGF 和 VEGF 做出反应,从而执行布尔逻辑运算。在没有蛋白质靶标的情况下,金纳米粒子最初作为红色溶液分散;靶蛋白的加入会导致纳米粒子聚集,使溶液变为蓝色,并释放出带有荧光染料标记的适体探针,从而导致荧光强度增加。这些输出构成了用于同时检测蛋白质的与门或或门。我们相信,这种基于逻辑门的检测系统将成为用于诊断应用的新型快速、廉价且可靠传感器的基础。