Supplemental Datasets for "SPIDR enables multiplexed mapping of RNA-protein interactions and uncovers a mechanism for selective translational suppression upon cell stress"

Published: 16 July 2025| Version 2 | DOI: 10.17632/2f8czsk233.2
Contributors:
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Description

Below is a brief description of each supplementary dataset. For more details, please see the Materials and Methods section of the manuscript here: https://doi.org/10.1101/2023.06.05.543769. Dataset S1: LC-MS/MS based protein quantification of the “Control IP”, 5 distinct “single RBP IPs” and “Pooled IP targeting 10 RBPs” (see STAR Methods for details), related to Figure S2. Dataset S2: LC-MS/MS based protein quantification of the “HEK293T total lysate” and the supernatants after the “Control IP”, 5 distinct “single RBP IPs” and “Pooled IP targeting 10 RBPs” (see STAR Methods for details), related to Figure S2. Dataset S3: LC-MS/MS based protein quantification of the “Control IP” and “Pooled IP targeting 39 RBPs” (see STAR Methods for details), related to Figure S1. Dataset S4: LC-MS/MS based protein quantification of the HEK293T total lysates generated either from “Control (Solvent)”- or “Torin1”-treated cells (see STAR Methods for details), related to Figure 7 and Table S6. Dataset S5: LC-MS/MS based protein quantification of the 4EBP1 IP from HEK293T lysates generated either from “Control (Solvent)”- or “Torin1”-treated cells (see STAR Methods for details), related to Figure S7. Dataset S6: LC-MS/MS based protein quantification of the IgG IP and V5 IP from HEK293T lysates (see STAR Methods for details), related to Figure S2.

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Steps to reproduce

Please refer to the method section in the paper which can be found of the manuscript here: https://doi.org/10.1101/2023.06.05.543769

Institutions

Columbia University, University of Michigan, Loyola Marymount University, California Institute of Technology, University of California Merced

Categories

RNA-Binding Protein, High-Throughput Sequencing

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