Protocol for Nanodisc single-molecule pull-down assay to detect protein-lipid interactions

Phospholipids function as signaling molecules regulating numerous processes within the cellular environment. Identifying and characterizing the protein players involved in lipid-mediated functions remains a central focus. Here, we present a protocol for evaluating lipid-protein interactions using mammalian whole-cell lysates expressing proteins of interest in a single-molecule pull-down (SiMPull) assay. We describe steps for preparing materials and slide chambers, performing SiMPull, and analyzing data. Nanodiscs and total internal reflection fluorescence (TIRF) microcopy enable the detection of interactions at single-molecule resolution. For complete details on the use and execution of this protocol, please refer to Arauz et al.<sup>1</sup> and Reyes-Ordoñez et al.<sup>2</sup>.

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Publication Details

Journal
STAR Protocols
Published
2026-02-17
DOI
https://doi.org/10.1016/j.xpro.2026.104377
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
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article

Protocol for Nanodisc single-molecule pull-down assay to detect protein-lipid interactions

Shweta Shree, Jie Chen, Stephen G. Sligar, Adriana Reyes-Ordoñez
STAR Protocols
Advanced Fluorescence Microscopy Techniques
article

Protocol for Nanodisc single-molecule pull-down assay to detect protein-lipid interactions

Shweta Shree, Jie Chen, Stephen G. Sligar, Adriana Reyes-Ordoñez
article en

Abstract

Phospholipids function as signaling molecules regulating numerous processes within the cellular environment. Identifying and characterizing the protein players involved in lipid-mediated functions remains a central focus. Here, we present a protocol for evaluating lipid-protein interactions using mammalian whole-cell lysates expressing proteins of interest in a single-molecule pull-down (SiMPull) assay. We describe steps for preparing materials and slide chambers, performing SiMPull, and analyzing data. Nanodiscs and total internal reflection fluorescence (TIRF) microcopy enable the detection of interactions at single-molecule resolution. For complete details on the use and execution of this protocol, please refer to Arauz et al.<sup>1</sup> and Reyes-Ordoñez et al.<sup>2</sup>.

STAR ProtocolsVol. 7(1)
University of Illinois Urbana-Champaign (US)
Openalex Percentile: Top 58%
Advanced Fluorescence Microscopy Techniques
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