2 research outputs found
Optimization of the Production of Covalently Circularized Nanodiscs and Their Characterization in Physiological Conditions
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
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>