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The homological resemblance between thyroxine (TH) and particular TH-disrupting chemicals (TH-EDCs), such as PCB metabolites, dioxin (PCDD), and brominated flame retardants, results in binding to the high-affinity TH transport protein, transthyretin TTR, thereby obstructing T4-TTR binding (Miyawaki et al., 2007)

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Interestingly, the difference in activity compared to cell surface HRP and APEX2 in this context was considerably smaller than the activity difference observed for biotinylation on living cells

doi: 10.1111/1751-7915.13524 138 XuJ.YangY

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Zhou S, Zhu J, Sun X, Xie L, Zhao Y, Ding S, et al