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1. FRET-Based Ca2+ Biosensor Single Cell Imaging Interrogated by High-Frequency Ultrasound

   https://doi.org/10.3390/s20174998  

   Yoon, Sangpil; Pan, Yijia; Shung, Kirk; Wang, Yingxiao (September 2020, Sensors)

   null (Ed.)

   Fluorescence resonance energy transfer (FRET)-based biosensors have advanced live cell imaging by dynamically visualizing molecular events with high temporal resolution. FRET-based biosensors with spectrally distinct fluorophore pairs provide clear contrast between cells during dual FRET live cell imaging. Here, we have developed a new FRET-based Ca2+ biosensor using EGFP and FusionRed fluorophores (FRET-GFPRed). Using different filter settings, the developed biosensor can be differentiated from a typical FRET-based Ca2+ biosensor with ECFP and YPet (YC3.6 FRET Ca2+ biosensor, FRET-CFPYPet). A high-frequency ultrasound (HFU) with a carrier frequency of 150 MHz can target a subcellular region due to its tight focus smaller than 10 µm. Therefore, HFU offers a new single cell stimulations approach for FRET live cell imaging with precise spatial resolution and repeated stimulation for longitudinal studies. Furthermore, the single cell level intracellular delivery of a desired FRET-based biosensor into target cells using HFU enables us to perform dual FRET imaging of a cell pair. We show that a cell pair is defined by sequential intracellular delivery of the developed FRET-GFPRed and FRET-CFPYPet into two target cells using HFU. We demonstrate that a FRET-GFPRed exhibits consistent 10–15% FRET response under typical ionomycin stimulation as well as under a new stimulation strategy with HFU. 

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2. Optimizing locked nucleic acid modification in double-stranded biosensors for live single cell analysis

   https://doi.org/10.1039/d1an01802g  

   Vilchez Mercedes, Samuel A.; Eder, Ian; Ahmed, Mona; Zhu, Ninghao; Wong, Pak Kin (January 2022, The Analyst)

   Double-stranded (ds) biosensors are homogeneous oligonucleotide probes for detection of nucleic acid sequences in biochemical assays and live cell imaging. Locked nucleic acid (LNA) modification can be incorporated in the biosensors to enhance the binding affinity, specificity, and resistance to nuclease degradation. However, LNA monomers in the quencher sequence can also prevent the target-fluorophore probe binding, which reduces the signal of the dsLNA biosensor. This study investigates the influence of LNA modification on dsLNA biosensors by altering the position and amount of LNA monomers present in the quencher sequence. We characterize the fluorophore–quencher interaction, target detection, and specificity of the biosensor in free solution and evaluate the performance of the dsLNA biosensor in 2D monolayers and 3D spheroids. The data indicate that a large amount of LNA monomers in the quencher sequence can enhance the specificity of the biosensor, but prevents effective target binding. Together, our results provide guidelines for improving the performance of dsLNA biosensors in nucleic acid detection and gene expression analysis in live cells. 

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3. Hybridization and self‐assembly behaviors of surface‐immobilized DNA in close proximity: A single‐molecule perspective: Nanoscience: Special Issue Dedicated to Professor Paul S. Weiss

   https://doi.org/10.1002/agt2.186  

   Gu, Qufei; Josephs, Eric A.; Ye, Tao (February 2022, Aggregate)

   Abstract Solid surfaces that are immobilized with DNA molecules underlie an array of biotechnological devices. These surfaces may also mediate the self‐assembly of hierarchical DNA nanostructures. However, a number of fundamental questions concerning the structure–function relationship of these biointerfaces remain, including how these DNA probe molecules organize on the surface and how the spatial organization influences molecular recognition kinetics and interfacial affinity of these DNA molecules at the regime where crowding interactions are important (1–10 nm). This mini‐review covers recent advances in understanding this structure–function relationship by spatially resolving surface hybridization events at the single‐molecule level. Counterintuitive cooperative effects in surface hybridization are discussed and as is how modeling these cooperative effects can be used to predict the hybridization kinetics of a prototypical DNA sensor. Future opportunities in using mechanistic understanding to improve the performance and reliability of DNA sensors and form hierarchical supramolecular structures are also discussed. 

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4. DNA NANOTECHNOLOGY: THE DEVELOPMENT OF MULTI-FUNCTIONAL HYBRIDIZATION SENSORS

   MUELLER, Brittany L (December 2024, University of Central Florida https://stars.library.ucf.edu/etd2024/55/)

   Hybridization probes have been used to detect specific nucleic acids for the last 50 years. These probes have applications in medicine, including identifying disease-causing genes or multi-drug resistant bacteria. To be considered robust, a probe should have high selectivity at ambient or low temperatures, be able to detect folded analytes, and remain economical for use in clinical settings. This work will uncover a challenge faced by molecular beacon probes (MBP), describe an adaptation to a molecular beacon probe (MBP) that enables the hybridization of the probe to a folded target, a multicomponent DNA sensor (OWL2) that overcomes common challenges faced by hybridization probes, and a thresholding sensor (MB-Th) that allows for the quantification of microRNA. Through the use of unwinding arms, the MBP adaptation and OWL2 sensor are able to hybridize with and detect folded analytes. Additionally, the OWL2 sensor contains two analyte-binding arms to unwind folded analytes and two sequence-specific strands that bind both the analyte and a universal molecular beacon (UMB) probe to form a fluorescent ‘OWL’ structure. The sensor can differentiate single base mismatches in folded analytes in the temperature range of 5–38 °C, even when challenged with excess wild-type analytes. The MB-Th sensor consists of two gates with increasing affinity for the target, with each varying in thermodynamic stability. The gates bind to separate molecular beacons, each with a unique fluorophore, and produce distinct signals that can be measured simultaneously. Both sensor designs are cost-efficient since the same UMB probe can be used to detect any analyte sequence. These sensors have significant clinical benefits for the diagnosis of non-invasive early-stage cancer and cancers associated with miRNA dysregulation. iv 

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5. The Effects of Three-Dimensional Ligand Immobilization on Kinetic Measurements in Biosensors

   https://doi.org/10.3390/polym14020241  

   Chiodi, Elisa; Marn, Allison M.; Bakhshpour, Monireh; Lortlar Ünlü, Nese; Ünlü, M. Selim (January 2022, Polymers)

   The field of biosensing is in constant evolution, propelled by the need for sensitive, reliable platforms that provide consistent results, especially in the drug development industry, where small molecule characterization is of uttermost relevance. Kinetic characterization of small biochemicals is particularly challenging, and has required sensor developers to find solutions to compensate for the lack of sensitivity of their instruments. In this regard, surface chemistry plays a crucial role. The ligands need to be efficiently immobilized on the sensor surface, and probe distribution, maintenance of their native structure and efficient diffusion of the analyte to the surface need to be optimized. In order to enhance the signal generated by low molecular weight targets, surface plasmon resonance sensors utilize a high density of probes on the surface by employing a thick dextran matrix, resulting in a three-dimensional, multilayer distribution of molecules. Despite increasing the binding signal, this method can generate artifacts, due to the diffusion dependence of surface binding, affecting the accuracy of measured affinity constants. On the other hand, when working with planar surface chemistries, an incredibly high sensitivity is required for low molecular weight analytes, and furthermore the standard method for immobilizing single layers of molecules based on self-assembled monolayers (SAM) of epoxysilane has been demonstrated to promote protein denaturation, thus being far from ideal. Here, we will give a concise overview of the impact of tridimensional immobilization of ligands on label-free biosensors, mostly focusing on the effect of diffusion on binding affinity constants measurements. We will comment on how multilayering of probes is certainly useful in terms of increasing the sensitivity of the sensor, but can cause steric hindrance, mass transport and other diffusion effects. On the other hand, probe monolayers on epoxysilane chemistries do not undergo diffusion effect but rather other artifacts can occur due to probe distortion. Finally, a combination of tridimensional polymeric chemistry and probe monolayer is presented and reviewed, showing advantages and disadvantages over the other two approaches. 

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