Skip to Content
Merck
CN
  • Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay.

Analysis of transient membrane protein interactions by single-molecule diffusional mobility shift assay.

Experimental & molecular medicine (2021-02-20)
Min Gyu Jeong, Kai Zhou, Soyeon Park, HyeongJeon An, Yonghoon Kwon, Yeonho Chang, Do-Hyeon Kim, Sung Ho Ryu
ABSTRACT

Various repertoires of membrane protein interactions determine cellular responses to diverse environments around cells dynamically in space and time. Current assays, however, have limitations in unraveling these interactions in the physiological states in a living cell due to the lack of capability to probe the transient nature of these interactions on the crowded membrane. Here, we present a simple and robust assay that enables the investigation of transient protein interactions in living cells by using the single-molecule diffusional mobility shift assay (smDIMSA). Utilizing smDIMSA, we uncovered the interaction profile of EGFR with various membrane proteins and demonstrated the promiscuity of these interactions depending on the cancer cell line. The transient interaction profile obtained by smDIMSA will provide critical information to comprehend the crosstalk among various receptors on the plasma membrane.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Cysteamine, ≥98.0% (RT)
Sigma-Aldrich
Protocatechuate 3,4-Dioxygenase from Pseudomonas sp., lyophilized powder, ≥3 units/mg solid
Sigma-Aldrich
Anti-c-ErbB2/c-Neu (Ab-5) Mouse mAb (TA-1), liquid, clone TA-1, Calbiochem®
Sigma-Aldrich
Monoclonal Anti-EPHA2 antibody produced in mouse, clone 6F8, purified immunoglobulin, buffered aqueous solution
Sigma-Aldrich
Monoclonal Anti-PDGFRB antibody produced in mouse, clone 4C12, purified immunoglobulin, buffered aqueous solution