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1.
Nature ; 613(7943): 345-354, 2023 01.
Artículo en Inglés | MEDLINE | ID: mdl-36599983

RESUMEN

Understanding how a subset of expressed genes dictates cellular phenotype is a considerable challenge owing to the large numbers of molecules involved, their combinatorics and the plethora of cellular behaviours that they determine1,2. Here we reduced this complexity by focusing on cellular organization-a key readout and driver of cell behaviour3,4-at the level of major cellular structures that represent distinct organelles and functional machines, and generated the WTC-11 hiPSC Single-Cell Image Dataset v1, which contains more than 200,000 live cells in 3D, spanning 25 key cellular structures. The scale and quality of this dataset permitted the creation of a generalizable analysis framework to convert raw image data of cells and their structures into dimensionally reduced, quantitative measurements that can be interpreted by humans, and to facilitate data exploration. This framework embraces the vast cell-to-cell variability that is observed within a normal population, facilitates the integration of cell-by-cell structural data and allows quantitative analyses of distinct, separable aspects of organization within and across different cell populations. We found that the integrated intracellular organization of interphase cells was robust to the wide range of variation in cell shape in the population; that the average locations of some structures became polarized in cells at the edges of colonies while maintaining the 'wiring' of their interactions with other structures; and that, by contrast, changes in the location of structures during early mitotic reorganization were accompanied by changes in their wiring.


Asunto(s)
Células Madre Pluripotentes Inducidas , Espacio Intracelular , Humanos , Células Madre Pluripotentes Inducidas/citología , Análisis de la Célula Individual , Conjuntos de Datos como Asunto , Interfase , Forma de la Célula , Mitosis , Polaridad Celular , Supervivencia Celular
2.
ChemSusChem ; 16(23): e202300833, 2023 Dec 07.
Artículo en Inglés | MEDLINE | ID: mdl-37584184

RESUMEN

With the rapid development in perovskite solar cell (PSC), high efficiency has been achieved, but the long-term operational stability is still the most important challenges for the commercialization of this emerging photovoltaic technology. So far, bi-dopants lithium bis(trifluoromethylsulfonyl)-imide (Li-TFSI)/4-tert-butylpyridine (t-BP)-doped hole-transporting materials (HTM) have led to state-of-the art efficiency in PSCs. However, such dopants have several drawbacks in terms of stability, including the complex oxidation process, undesirable ion migration and ultra-hygroscopic nature. Herein, a fluorine-containing organic Lewis acid dopant bis(pentafluorophenyl)zinc (Zn-FP) with hydrophobic property and high migration barrier has been employed as a potential alternative to widely employed bi-dopants Li-TFSI/t-BP for poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine] (PTAA). The resulting Zn-FP-based PSCs achieve a maximum PCE of 20.34 % with hysteresis-free current density-voltage (J-V) scans. Specifically, the unencapsulated device exhibits a significantly advanced of operational stability under the International Summit on Organic Photovoltaic Stability protocols (ISOS-L-1), maintaining over 90 % of the original efficiency after operation for 1000 h under continuous 1-sun equivalent illumination in N2 atmosphere in both forward and reverse J-V scan.

3.
ACS Appl Mater Interfaces ; 12(24): 27526-27536, 2020 Jun 17.
Artículo en Inglés | MEDLINE | ID: mdl-32423198

RESUMEN

Conventional electrochromic devices with a sandwich structure consist of multiple interfaces, which enhance electron trapping on the interfaces. Furthermore, crack generation in the electrochromic layer is inevitable due to repeated ion insertion and extraction during the service process. These problems increase the fabrication complexity and lead to poor performance and stability, which are severely limiting and prime concerns for the future development of the electrochromism field. Here, a strategy of synthesizing an all-in-one self-healing electrochromic material, TAFPy-MA, is presented, which has been utilized for the fabrication of a high-reliability, large-scale, and easy-assembly smart electrochromic window. The all-in-one self-healing electrochromic material can undergo in situ redox reactions with Li+ ions to reduce resistance transfer and avoid interface obstacles, and the reversible Diels-Alder cross-linking network structure can heal the cracks to improve the reliability of the electrochromic layer. High ion diffusivity (1.13 × 10-5 cm2 s-1), rapid color switching (3.9/3.7 s), high coloration efficiency (413 cm2 C-1), excellent stability (sustains 88.7% after 1000 cycles) and reliability (crack can be healed in 110 s), and large-scale smart windows (30 × 35 cm2) are achieved using the all-in-one electrochromic material, which exhibits fascinating and promising features for a wide range of applications in buildings, airplanes, etc.

4.
Stem Cell Reports ; 12(5): 1145-1158, 2019 05 14.
Artículo en Inglés | MEDLINE | ID: mdl-30956114

RESUMEN

We describe a multistep method for endogenous tagging of transcriptionally silent genes in human induced pluripotent stem cells (hiPSCs). A monomeric EGFP (mEGFP) fusion tag and a constitutively expressed mCherry fluorescence selection cassette were delivered in tandem via homology-directed repair to five genes not expressed in hiPSCs but important for cardiomyocyte sarcomere function: TTN, MYL7, MYL2, TNNI1, and ACTN2. CRISPR/Cas9 was used to deliver the selection cassette and subsequently mediate its excision via microhomology-mediated end-joining and non-homologous end-joining. Most excised clones were effectively tagged, and all properly tagged clones expressed the mEGFP fusion protein upon differentiation into cardiomyocytes, allowing live visualization of these cardiac proteins at the sarcomere. This methodology provides a broadly applicable strategy for endogenously tagging transcriptionally silent genes in hiPSCs, potentially enabling their systematic and dynamic study during differentiation and morphogenesis.


Asunto(s)
Sistemas CRISPR-Cas , Edición Génica/métodos , Células Madre Pluripotentes Inducidas/metabolismo , Miocitos Cardíacos/metabolismo , Sarcómeros/genética , Actinina/genética , Actinina/metabolismo , Secuencia de Aminoácidos , Diferenciación Celular/genética , Línea Celular , Reparación del ADN por Unión de Extremidades/genética , Regulación de la Expresión Génica , Proteínas Fluorescentes Verdes/genética , Proteínas Fluorescentes Verdes/metabolismo , Humanos , Células Madre Pluripotentes Inducidas/citología , Miocitos Cardíacos/citología , Sarcómeros/metabolismo , Homología de Secuencia de Aminoácido , Troponina I/genética , Troponina I/metabolismo
5.
ACS Appl Mater Interfaces ; 10(41): 35533-35538, 2018 Oct 17.
Artículo en Inglés | MEDLINE | ID: mdl-30226978

RESUMEN

Animals such as chameleons possess a natural ability to adjust their skin color as a preventive measure to deter any potential threat and to self-heal damaged skin tissues. Inspired by this, we present here a copolymer film possessing biomimetic properties that simultaneously integrates electrochromic triphenylamine and self-healing Diels-Alder groups. The flexible and stretchable copolymer film acts like natural chameleon skin, which exhibits significant color variation and also possesses excellent self-healing properties. These remarkable features make it a promising material for overcoming the crack-generation issue inherited by conventional biomimetic chameleon skin. Moreover, a flexible and wearable skin device based on the copolymer film with silver fabric as a electrode has also been fabricated. The electrochromic and self-healing properties were verified for the copolymer film, and it has been elucidated that the intelligent biomimetic "chameleon skin" was a new step toward the development of highly advanced biomimetic materials and devices.


Asunto(s)
Materiales Biomiméticos/química , Color , Plata/química , Piel Artificial , Electrodos
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