Journal
NATURE PROTOCOLS
Volume 9, Issue 10, Pages 2382-2394Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2014.163
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Funding
- US National Institutes of Health (NIH) [R37AI020241, R01AI022571]
- Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq, Brazil) [305983/2011-3, 477475/2013-2]
- Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG, Brazil)
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Precise immunolocalization of proteins within a cell is central to understanding cell processes and functions such as intracellular trafficking and secretion of molecules during immune responses. Here we describe a protocol for ultrastructural detection of proteins in leukocytes. The method uses a pre-embedding approach (immunolabeling before standard processing for transmission electron microscopy (TEM)). This protocol combines several strategies for ultrastructure and antigen preservation, robust blocking of nonspecific binding sites, as well as superior antibody penetration for detecting molecules at subcellular compartments and membrane microdomains. A further advantage of this technique is that electron microscopy (EM) processing is quick. This method has been used to study leukocyte biology, and it has helped demonstrate how activated leukocytes deliver specific cargos. It may also potentially be applied to a variety of different cell types. Excluding the initial time required for sample preparation (15 h) and the final resin polymerization step (16 h), the protocol (immunolabeling and EM procedures) can be completed in 8 h.
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