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Expression, Detergent Solubilization, and Purification of a Membrane Transporter, the MexB Multidrug Resistance Protein
Published on: December 3, 2010
Detergent-resistant domains in Spodoptera frugiperda midgut microvillar membranes and their relation to microapocrine
Felipe J Fuzita1, Daniel C Pimenta2, Giuseppe Palmisano3
1Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, Avenida Professor Lineu Prestes, 748, São Paulo 05508-000, Brazil.
Abstract:
The midgut from lepidopteran insects has a particular way to release proteins to the lumen, named microapocrine secretion that could be an adaptation to release secretory contents into the lumen at water absorbing regions. In this process small vesicles (microapocrine vesicles) bud from the midgut microvilli as double membrane vesicles, where the inner membrane comes from the secretion vesicle and the outer one from the microvillar membrane. The molecular machinery associated with this process may be recruited by specific midgut microvilli membrane domains. To address to this, Spodoptera frugiperda midgut microvillar membranes, prepared by magnesium treatment and free from cytoskeleton with the hyperosmotic Tris procedure, were submitted to detergent extraction and fractionated by density gradient ultracentrifugation. Detergent-resistant membrane domains (DRM) were recovered and their proteins identified by proteomics. Microapocrine vesicles were isolated by washing the luminal surface of the midgut epithelium, followed by freezing and thawing plus centrifugation to recover only membranes. Proteins from purified microvillar membranes and microapocrine vesicle membranes were identified by proteomics. Comparison of the two populations suggests that the budding of microapocrine vesicles surrounded by microvillar membrane is not a random process, because only around 50% of the microvillar membrane proteins are in the microapocrine vesicles. From the 16 proteins from DRM, 14 were enriched in the microapocrine membrane vesicles. These results suggest that on budding, the microapocrine vesicle membrane is enclosed by DRM and a surrounding area of the microvillar membrane. It is proposed that the DRMs somehow recruit the proteins composing the secretory machinery.
Insights
Insect midgut cells use microapocrine secretion to release proteins via vesicles. This study found that detergent-resistant membrane domains (DRMs) are key to recruiting proteins for this specialized secretion process.
Area of Science:
- Insect biology
- Cellular secretion mechanisms
- Proteomics
Background:
- Lepidopteran insects possess a unique protein release method called microapocrine secretion.
- This process involves double-membraned vesicles budding from midgut microvilli, potentially aiding secretion in water-absorbing regions.
Purpose of the Study:
- To investigate the molecular machinery and membrane domains involved in microapocrine secretion.
- To determine if specific microvillar membrane domains recruit proteins for vesicle budding.
Main Methods:
- Preparation of Spodoptera frugiperda midgut microvillar membranes, removing cytoskeleton.
- Detergent extraction and density gradient ultracentrifugation to isolate detergent-resistant membrane domains (DRMs).
- Proteomic analysis of microvillar membranes, DRMs, and isolated microapocrine vesicles.
Main Results:
- Microapocrine vesicle budding is not random, with only about 50% of microvillar membrane proteins incorporated.
- Of 16 DRM proteins identified, 14 were enriched in microapocrine vesicle membranes.
- Microapocrine vesicle membranes are enclosed by DRMs and adjacent microvillar membrane areas.
Conclusions:
- The microapocrine secretion process involves specific recruitment of proteins by DRMs within the microvillar membrane.
- DRMs play a crucial role in organizing the molecular machinery for microapocrine vesicle formation and secretion.
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