| Literature DB >> 30886003 |
Ranjan Sengupta1, Michael J Poderycki1, Seema Mattoo2.
Abstract
We describe a method, termed cryoAPEX, which couples chemical fixation and high-pressure freezing of cells with peroxidase tagging (APEX) to allow precise localization of membrane proteins in the context of a well-preserved subcellular membrane architecture. Further, cryoAPEX is compatible with electron tomography. As an example, we apply cryoAPEX to obtain a high-resolution three-dimensional contextual map of the human FIC (filamentation induced by cAMP) protein, HYPE (also known as FICD). HYPE is a single-pass membrane protein that localizes to the endoplasmic reticulum (ER) lumen and regulates the unfolded protein response. Alternate cellular locations for HYPE have been suggested. CryoAPEX analysis shows that, under normal and/or resting conditions, HYPE localizes robustly within the subdomains of the ER and is not detected in the secretory pathway or other organelles. CryoAPEX is broadly applicable for assessing both lumenal and cytosol-facing membrane proteins.Entities:
Keywords: CryoAPEX; Cryofixation; Electron tomography; FIC AMPylation; Membrane protein
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Year: 2019 PMID: 30886003 PMCID: PMC6451417 DOI: 10.1242/jcs.222315
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285