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• W4387356909 abstract "Calcium ion (Ca2+) serves as a ubiquitous second messenger within eukaryotic cells. Alterations in free Ca2+ concentration, known as Ca2+ signals,1 play a vital role in regulating a wide array of physiological and pathological processes, including synaptic transmission, muscle contraction, cytokine secretion, gene transcription, cell growth, and cell death.2 Abnormal Ca2+ signalling has been implicated in various human disorders such as cancer, immunodeficiency, myocardial hypertrophy, and neurodegenerative diseases.3 Ca2+ signals possess the capacity to convey crucial information through three-dimensional variations in amplitude, temporal and spatial distribution (Figure 1A). Over the past four decades, considerable efforts have been devoted to developing biosensors and actuators aimed at interrogating these three fundamental properties of Ca2+ signals.4 Given their facile genetic manipulation and tunable sensitivity, genetically encoded Ca2+ indicators (GECIs) have gained widespread popularity for tracking intracellular Ca2+ signals or Ca2+-modulated cell activities.5 A typical GECI comprises a Ca2+-sensing moiety (sensor) and a fluorescence reporting module (reporter). Upon binding or dissociation of Ca2+, the sensor often undergoes conformational changes that modify the spectral properties and/or brightness of the reporter,6 thereby enabling real-time observation of Ca2+ signals by quantifying changes in fluorescence intensities (F) (Figure 1B). By driving their expression under tissue-specific promoters or via fusion with the organelle-targeting moieties, GECIs can be precisely expressed in particular cell types or subcellular compartments, hence facilitating the accurate reporting of spatial attributes of Ca2+ signal. Through several generations of evolution over the past two decades, GECIs have shown significantly enhanced sensitivity and diversified kinetics.6 Among them, the latest jGCaMP8f exhibits an impressive activation half-time of 2 ms, which enables better decoding of fast-acting Ca2+ signals seen in excitable cells including neurons and cardiomyocytes.7 Nonetheless, the advancements in their intracellular dynamics, particularly the capacity of GECIs to resolve subtle Ca2+ signal amplitudes, have progressed at a comparatively slower pace since the inception of the GCaMP6 series. The dynamics of GECIs are commonly gauged by the dynamic range (DR) or the signal-to-baseline ratio (SBR). DR represents the responsive capacity of GECI, which is calculated from its fluorescence intensity at Ca2+-saturated (Fmax) or Ca2+-free states (Fmin) and expressed as (Fmax—Fmin)/Fmin.8 By comparison, SBR is a more physiologically-relevant metric, defined as the ratio of the change in the fluorescence intensity (F—F0, or ΔF) over the basal fluorescence intensity (F0). Among the green GECIs utilizing circularly permuted enhanced green fluorescent protein (cpEGFP) as the reporter (Figure 1B), the GCaMP6 series remains the most prevalent. The in-cellulo DRs of GCaMP6 and its updated version jGCaMP7c measure in the range of 20–30,9 and the latest jGCaMP8s exhibits a DR of only 4.1. Overall, a notable technical gap persists in the field of GECIs, necessitating the creation of biosensors with increased DR or enhanced SBR. A technical leap in this direction will likely enable more accurate and sensitive detection of subtle fluctuations in Ca2+ signals. The development of GCaMP variants with an expanded DR faces a significant hurdle due to the constraint imposed by the relatively low brightness of the cpEGFP reporter. A recent breakthrough, leveraging a brighter fluorescent protein (mNeonGreen or mNG, possessing nearly 3-fold higher brightness than EGFP), has led to the creation of a new series of ultra-sensitive mNG-based calcium indicators, designated as NEMO (Figure 1C).10 NEMO indicators are generated through iterative optimization of the calcium-sensing module, the reporter, and the linkers connecting them. Five variants of NEMO with distinct optical properties have been created, with NEMOb, NEMOc, NEMOf, NEMOm and NEMOs representing bright, high-contrast, fast-acting, medium-response, and sensitive versions, respectively. Distinguished from the GCaMP series, NEMO exhibits a spectral profile that lies between GFP and YFP, forming a narrower spectrum. This unique attribute enables imaging using either GFP or YFP filters, as well as multiplexing with CFP. Further enhancing its utility, NEMO sensors exhibit enhanced resistance to photobleaching under more intense illumination, effectively broadening their scope of in vivo application. Of paramount significance, the NEMO variants exhibit superior dynamic ranges (>100) and SBR values, reaching an unprecedented level of up to 220. As aforementioned, a larger DR or SBR facilitates better resolution Ca2+ signal amplitudes. Indeed, NEMO sensors could resolve Ca2+ oscillations (Figure 2A) and store operated Ca2+ entry (SOCE) responses (Figure 2B) in non-excitable cells, as well as Ca2+ transients in neurons (Figure 2C), with much larger SBRs. During high-frequency electric field stimulation, NEMOc displayed a response amplitude exceeding that of GCaMP6 by more than 30 times. This remarkable improvement in SBR holds particular significance in deciphering signals within neurons or muscle cells, as the existing fast-acting GECIs tend to have smaller in-cellulo DRs. Prominent examples like GCaMP6f and jGCaMP7f possess DRs below 14 when expressed in mammalian cells, while the latest ultra-fast variant, jGCaMP8f, registers a mere DR of 3.7. In contrast, NEMOf, exhibiting comparable speed to GCaMP6f and jGCaMP7f, has a DR that surpasses these two fast GECIs by 17 times. The substantial improvement in DR positions NEMOf as an ideal tool for effectively decoding both frequency and amplitude information within neural circuits or other excitable cells. Furthermore, NEMOf provides an excellent template for further engineering aimed at enhancing its kinetics to match or even surpass jGCaMP8f while still maintaining a reasonable DR. The extra-large DR of NEMO indicators allows real-time quantification of subtle Ca2+ transients with enhanced sensitivity. These NEMO sensors have undergone rigorous validation in diverse settings, encompassing non-excitable cell lines, dissociated cultured rat neurons, acute mouse brain slices, in vivo two-photon laser imaging (Figure 2D), fibre recording of mouse brains, and plant cells. Under each scenario, NEMO variants have shown superior performance over the GCaMP6 series. Furthermore, compared to the GCaMP series, NEMO indicators remain relatively stable within the pH range of 6–9. This feature imparts greater resilience to physiological pH fluctuations and renders them suitable for detecting Ca2+ signals within cancer cells under hypoxia conditions. By optimizing the Ca2+-binding affinities and incorporating appropriate targeting sequences, modified NEMO indicators can be tailored to discern Ca2+ signals within acidic organelles like the endosomal compartments, as well as synaptic vesicles, secretory vesicles, and the trans-Golgi apparatus. Looking ahead, subcellular NEMO indicators may also hold the promise of effectively resolving localized Ca2+ signals at membrane contact sites formed between the endoplasmic reticulum and mitochondria, or the plasma membrane. In summary, in contrast to most existing GECIs, which often trade their DR for heightened sensitivity and faster kinetics, NEMO variants manage to maintain rapid responsiveness while preserving superior dynamic ranges for accurate Ca2+ signal reporting. Moreover, they exhibit substantially improved photostability, enabling them to withstand considerably stronger illumination, along with enhanced resistance to pH fluctuations. Collectively, these desirable characteristics position NEMO sensors as the preferred choice for monitoring Ca2+ dynamics within mammalian cells, tissues, living animals, as well as in plants. This work was supported by the Ministry of Science and Technology of China (2019YFA0802104 to Youjun Wang), the National Natural Science Foundation of China (91954205 and 92254301 to Youjun Wang), and the Welch Foundation (BE-1913−20220331 to Yubin Zhou). The authors declare no conflicts of interest." @default.
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• W4387356909 date "2023-10-01" @default.
• W4387356909 modified "2023-10-17" @default.
• W4387356909 title "Finding NEMO: The quest for next‐generation genetically encoded calcium indicators" @default.
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