Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:3.4.21.4 (trypsin)
 42,187 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Two electrophoretically different forms of estradiol receptor can be extracted from crude porcine endometrium microsomes with low ionic strength buffers. Better yields (approximately 50%) of both forms are obtained in the presence of Surfynol 485. Dithiothreitol boosts the solubilization of basic receptor. Together, Surfynol and dithiothreitol have a more than additive effect, amounting to 3-4 times the quantities of receptor extracted with plain buffer. Trypsin more than triples the yields obtained with Surfynol/dithiothreitol, while degrading both receptor forms to a characteristic fragment. Hyaluronoglucosaminidase is somewhat less effective than trypsin. It changes acidic receptor to basic. The proportions of acidic/basic receptor in microsomal subfractions are different. Rough endoplasmic reticulum contains almost exclusively basic receptor. Smooth membranes are rich in acidic receptor. The efficacy of both enzymes is closely related to the proportion of acidic receptor found in Surfynol/dithiothreitol extracts.
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PMID:Structural assignment and extractability of microsomal estradiol receptors. 662 40

The exhaustive extraction of microsomal estradiol receptor by Surfynol/dithiothreitol/trypsin in low ionic strength buffer was employed for distribution studies on non-stimulated porcine endometrium. It was found that more than half of the cytoplasmic receptor contents were of microsomal origin. "Empty" structures did not interfere with receptor analysis by agargel electrophoresis. The combined yields from homogenate fractions corresponded to those obtained from unfractionated homogenates. Freeze-fracturing of endometrium had a moderate receptor-solubilizing effect.
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PMID:Origin and quantification of cytoplasmic estradiol receptor in resting target cells. 666 99