Hi all,

I have purified an integral membrane transporter in lauryl maltose neopentyle glycol (LMNG) detergent. Protein seems happy in the detergent and can bind to the inhibitor. However, I want to study the transport of some compound with purified protein and for that I have to reconstitute the protein into liposome. LMNG has very low cmc (0.001%) and I wonder what would be the best way to remove the detergent for liposome formation. The typical methods such as dialysis, biobeads etc are useful for detergents with high cmc. Anyone ever tried these methods or any other method for LMNG removal?

Thanks in advance.

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