Abstract
SUMMARYThe recently developed single-molecule pulldown (SiMPull) assay by Jain and colleagues is a highly innovative technique but its wide application is hindered by the high technical barrier and time consumption. We report an innovative, agarose microbead-based approach for SiMPull. We used commercially available, pre-surface-functionalized agarose microbeads to capture the protein of interest together with its binding partners specifically from cell extracts and observed these interactions under a microscope at the single-molecule level. Relative to the original method, microbead-based SiMPull is considerably faster, easier to use, and more reproducible and yet provides similar sensitivity and signal-to-noise ratio; specifically, with the new method, sample-preparation time is substantially decreased (from ∼10 to ∼3 h). These crucial features should facilitate wide application of powerful and versatile SiMPull in common biological and clinical laboratories. Notably, by exploiting the simplicity and ultrahigh sensitivity of microbead-based SiMPull, we used this method in the study of rare auditory hair cells for the first time.
Publisher
Cold Spring Harbor Laboratory
Reference18 articles.
1. Real-time subpixel-accuracy tracking of single mitochondria in neurons reveals heterogeneous mitochondrial motion
2. Ballesteros, A. , Fenollar-Ferrer, C. , & Swartz, K. J. (2018). Structural relationship between the putative hair cell mechanotransduction channel TMC1 and TMEM16 proteins. ELife, 7. https://doi.org/10.7554/eLife.38433
3. Variable number of TMC1-dependent mechanotransducer channels underlie tonotopic conductance gradients in the cochlea;Nature Communications,2018
4. Ge, J. , Elferich, J. , Goehring, A. , Zhao, H. , Schuck, P. , & Gouaux, E. (2018). Structure of mouse protocadherin 15 of the stereocilia tip link in complex with LHFPL5. ELife, 7. https://doi.org/10.7554/eLife.38770
5. Hu, W. , Yu, X. , Liu, Z. , Sun, Y. , Chen, X. , Yang, X. , Li, X. , Lam, W. K. , Duan, Y. , Cao, X. , Steller, H. , Liu, K. , & Huang, P. (2017). The complex of TRIP-Br1 and XIAP ubiquitinates and degrades multiple adenylyl cyclase isoforms. ELife, 6. https://doi.org/10.7554/eLife.28021
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