Abstract:Membrane receptors, among other membrane proteins that universally exist on the cell surface, are a class of important macromolecules responsible for cellsignaling processes. They are activated or inhibited through selective binding with endogenous ligand molecules. These binding activities are implicated in physiologic as well as pathologic events if errors in signaling interactions occur. The thorough understanding of receptor-ligand recognition is of paramount importance for fundamental biological studies a… Show more
“…Fluorescent sensors continue to attract attention on account of their visualization ability and high sensitivity in detecting signals 1–3 . They can be applied in local microenvironments for monitoring the behavior of surrounding targets in various chemical and biological processes 4,5 , like charging cellular functional proteins 6 and membrane systems 7 . Although the past decades have witnessed a significant progress in design and development of typical donor–acceptor based π-structures with alterable fluorescence signals and ability to sense local environmental change 8 , a large majority of these fluorescent sensors work simply through the responsive variation of a single emission signal 9 .…”
Visualized sensing through fluorescence signals is a powerful method for chemical and physical detection. However, the utilization of fluorescent molecular probes still suffers from lack of precise signal self-calibration in practical use. Here we show that fluorescence and thermally activated delayed fluorescence can be simultaneously produced at the single-molecular level. The thermally activated delayed fluorescence serves as a sensing signal with its wavelength and lifetime both altered correlating to polarity, whereas the fluorescence always remains unchanged as an internal reference. Upon the establishment of a three-dimensional working curve upon the ratiometric wavelength and photoluminescence lifetime vs. polarity, disturbance factors during a relevant sensing process can be largely minimized by such a multiple self-calibration. This strategy was further applied into a precise detection of the microenvironmental polarity variation in complex phospholipid systems, towards providing new insights for convenient and accurate diagnosis of membrane lesions.
“…Fluorescent sensors continue to attract attention on account of their visualization ability and high sensitivity in detecting signals 1–3 . They can be applied in local microenvironments for monitoring the behavior of surrounding targets in various chemical and biological processes 4,5 , like charging cellular functional proteins 6 and membrane systems 7 . Although the past decades have witnessed a significant progress in design and development of typical donor–acceptor based π-structures with alterable fluorescence signals and ability to sense local environmental change 8 , a large majority of these fluorescent sensors work simply through the responsive variation of a single emission signal 9 .…”
Visualized sensing through fluorescence signals is a powerful method for chemical and physical detection. However, the utilization of fluorescent molecular probes still suffers from lack of precise signal self-calibration in practical use. Here we show that fluorescence and thermally activated delayed fluorescence can be simultaneously produced at the single-molecular level. The thermally activated delayed fluorescence serves as a sensing signal with its wavelength and lifetime both altered correlating to polarity, whereas the fluorescence always remains unchanged as an internal reference. Upon the establishment of a three-dimensional working curve upon the ratiometric wavelength and photoluminescence lifetime vs. polarity, disturbance factors during a relevant sensing process can be largely minimized by such a multiple self-calibration. This strategy was further applied into a precise detection of the microenvironmental polarity variation in complex phospholipid systems, towards providing new insights for convenient and accurate diagnosis of membrane lesions.
“…After centrifugation, the thin‐layer glycosheets (Gal‐sheet and Fuc‐sheet, which contain galactose‐ and fucose‐functionalized molecular layers, respectively) were obtained and used for antimicrobial assays. The molecular self‐assembly enables the multivalent display of the carbohydrate epitopes on the surface of MoS 2 , thereby enhancing their binding avidity with the lectins on the surface of bacteria, facilitating the subsequent light‐driven bacterial killing (Figure b).…”
With the evergrowing threat posed by multidrug resistance of bacteria, the development of effective antibacterial agents remains a global challenge. Infection with multidrug-resistant bacteria in hospitals significantly impairs the healing of wounds caused by deep-burn injuries or diabetic foot ulceration, leading to a high mortality rate among these patients. A multivalent glycosheet for the double light-driven therapy against multidrugresistant Pseudomonas aeruginosa (P. aeruginosa) infection on wounds is developed here. Galactose-and fucose-based ligands are self-assembled to form a glyco-layer on the surface of thin-layer molybdenum disulfide, producing the glycosheets capable of selectively localizing P. aeruginosa through multivalent carbohydrate-lectin interactions. The glycosheets loaded with antibiotics have proven applicable for: 1) near-infrared-light driven, in situ thermal release of antibiotics, increasing bacterial membrane permeability, and 2) white light-driven reactive-oxygen-species production to more thoroughly kill the bacteria. The targetability, together with the light sensibility, of the glycosheets enables a highly effective and optically controlled therapeutic regime for the healing of wounds infected by multidrug-resistant as well as clinically isolated P. aeruginosa.
“…[1] In many cases,s elective receptor-ligand recognition is the initial step for activating cellular function and defining cell fate. [2] At the nanoscale,the spatial organization of cell surface receptors plays pivotal role in controlling cellular signaling cascades. [3] Many cell behaviors (such as cell adhesion, spreading,growth, and migration) are known to be regulated by the clustering of cell surface receptors.…”
The spatial organization of cell‐surface receptors plays an important role in defining cell fate. Recently, the development of strategies for the direct regulation of receptor clustering using nanomaterials has aroused enormous interest. In this review, we discuss the mechanisms and features of recently developed nanomaterial‐based strategies to control the nanoscale distribution of cell binding ligands and regulate cell behavior. We expect this review to inspire innovative work on manipulating cell functions by controlling the clustering of cell surface receptors.
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