2 research outputs found

    Optimization of the Production of Covalently Circularized Nanodiscs and Their Characterization in Physiological Conditions

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    Lipid nanodiscs are widely used platforms for studying membrane proteins in a near-native environment. Lipid nanodiscs made with membrane scaffold proteins (MSPs) in the linear form have been well studied. Recently, a new kind of nanodisc made with MSPs in the circular form, referred to as covalently circularized nanodiscs (cNDs), has been reported to have some possible advantages in various applications. Given the potential of nanodisc technology, researchers in the field are very interested in learning more about this new kind of nanodisc, such as its reproducibility, production yield, and the possible pros and cons of using it. However, research on these issues is lacking. Here, we report a new study on nanodiscs made with circular MSPs, which are produced from a method different from the previously reported method. We show that our novel production method, detergent-assisted sortase-mediated ligation, can effectively avoid high-molecular-weight byproducts and also significantly improve the yield of the target proteins up to around 80% for larger circular MSP constructs. In terms of the application of circular MSPs, we demonstrate that they can be used to assemble nanodiscs using both synthetic lipids and native lipid extract as the source of lipids. We also show that bacteriorhodopsin can be successfully incorporated into this new kind of cND. Moreover, we found that cNDs have improved stability against both heat and high-concentration-induced aggregations, making them more beneficial for related applications

    Membrane Charging and Swelling upon Calcium Adsorption as Revealed by Phospholipid Nanodiscs

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    Direct binding of calcium ions (Ca<sup>2+</sup>) to phospholipid membranes is an unclarified yet critical signaling pathway in diverse Ca<sup>2+</sup>-regulated cellular phenomena. Here, high-pressure-liquid-chromatography, small-angle X-ray scattering (SAXS), UV–vis absorption, and differential refractive index detections are integrated to probe Ca<sup>2+</sup>-binding to the zwitterionic lipid membranes in nanodiscs. The responses of the membranes upon Ca<sup>2+</sup>-binding, in composition and conformation, are quantified through integrated data analysis. The results indicate that Ca<sup>2+</sup> binds specifically into the phospholipid headgroup zone, resulting in membrane charging and membrane swelling, with a saturated Ca<sup>2+</sup>-lipid binding ratio of 1:8. A Ca<sup>2+</sup>-binding isotherm to the nanodisc is further established and yields an unexpectedly high binding constant <i>K</i> = 4260 M<sup>–1</sup> and a leaflet potential of ca. 100 mV based on a modified Gouy–Chapman model. The calcium-lipid binding ratio, however, drops to 40% when the nanodisc undergoes a gel-to-fluid phase transition, leading to an effective charge capacity of a few μF/cm<sup>2</sup>
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