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investinational drug

Published by: cfz 2010-03-17
  • II. An investigational drug was synthesized by a graduate student in your laboratory, and it appears SERTRAN increases the release of serotonin (a neurotransmitter) in mice. The drug itself is a small, lipid soluble compound resembling a guanine nucleotide, but with a long, hydrophobic side chain that could interact with the side chains of amino acids on the surface of internal cellular proteins if brought into close proximity. Preliminary work consisting of in vivo labeling of known serotonin producing cells (by treating mice with a FITC fluorescent labeled drug) indicates this compound is associated with neuronal axonal transport pathways. You remember from your Cell Biology II Course that small G-proteins, like Rab, are involved in this pathway. (A) Describe a simple co-localization experiment that will show you by light microscopy whether or not this drug is binding to a Rab related protein. (B) Assuming you actually see a positive result in Part A, describe an experiment that would show if this drug enhances the binding of Rab to Syntaxin, a protein found on the inner face of the pre-synaptic neuronal membrane.(i need all answer in deep, so pl discribe in brief)
  • investinational drug - portal.dballastages.com - Powered by chcms::
    II. An investigational drug was synthesized by a graduate student inyour laboratory, and it appears SERTRAN increases the release ofserotonin (a
    http://portal.dballastages.com/gtrtfw/investinational-drug/pz1answersz3hgoogleb0iczvanswersczvthreadviewczvidczv88549z8hl/
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    International Labeling Requirements for Medical Devices, Medical - Google Books Result::
    href=http://books.google.com/books?id=GQCAdkf91vAC&pg=RA6-PA68&lpg=RA6-PA68&dq=investinational+drug&source=bl&ots=pu2z6nw09_&sig=h--M_3LVs4SC04r2ZgaT-Va6kJo&hl=en&ei=u4d1SrzfCIaysgPa48H1CA&sa=X&oi=book_result&ct=result&resnum=5 class=l onmousedown=return clk(this.href,,,res,5,)>International Labeling Requirements for Medical Devices, Medical - Google Books Resultby Charles B. Sidebottom - 2003 - Medical - 580 pages 425-426 intended use, 416-417 intraocular lenses, 424-425 investi national uses. 419-425 licensing. 266-268 Canada, see also Food and Drugs Act
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  • What does the phrase "(i need all answer in deep, so pl discribe in brief)" mean?


  • Thank you for the question. Because of the relatively high price for the question, I felt that it was important to get the best possible answer from a microbiology specialist as quickly as possible. To do this, I contacted a professional microbiologist, who recommends the following experimental protocols: For part A: 1. Treat the known serotonin-producing cells (from paragraph one) with a non-hydrolysable analogue of GTP such that all the vesicles fuse with the target membranes 2. Treating simultaneously with the FITC-labelled drug in from the first part, fix the known serotonin-producing cells and stain the preparation with a fluorescently-labelled antibody against Rab (use a different fluorescence to FITC). 3. Take pictures using the fluorescent 'scope. 4. Use the camera's imaging software to superimpose the two images (i.e. the green and red staining from the FITC-labelled drug and the labelled antibody) 5. Look for the third colour (i.e. yellow, in the areas of co-localization). ----------------Part B----------- For part B: 1. Using the serotonin-secreting cells from paragraph one, again treat with the non-hydrolysable analogue of GTP to encourage all the vesicles to fuse with the pre-synaptic membrane, which should encourage the Rab and syntaxin to make contact. 2. Make cell lysates at this point and do a co-immunoprecipitation experiment with the anti-Rab antibodies (from my answer in part A). 3. If Rab and syntaxin are associated, then syntaxin will be brought down in the co-IP. 4. The co-IP'ed protein can then be resolved by SDS-PAGE and Western blotted with anti-syntaxin antibodies. Note: You will do appropriate controls and show that there is more syntaxin brought down with Rab when the drug is used versus no drug control; you have to control the IP too with appropriate negative controls.
  • investinational drug::
    Subject: investinational drug. Category: Science > Biology Asked by: jimmy1978-ga. List Price: $100.00, Posted: 23 Oct 2002 06:50 PDT
    http://answers.google.com/answers/threadview/id/88549.html
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    Department of Health and Human Services::
    File Format: PDF/Adobe Acrobat - View as HTMLthe administration of the investinational rw\* drug. a specific uritten info&ation sheet cuntaming specrfibd dormation. Section 50.23(di(li(xivl reauires
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  • Regarding part A, since a fluorescent scope may not be permitted as a light scope is requested, for a light scope, try the following: Treat the serotonin-secreting cells with: 1. The drug, (that is supposed to increase vesicle fusion and serotonin release). 2. No drug, (control; so you won't see vesicle release from the pre-synaptic membranes). 3. A drug to inhibit the guanine nucleotide exchange factor which is required such that Rab can exchange GDP for GTP and allow vesicle fusion (so no vesicle fusion should be observed in this case). These different conditions could be viewed under the light microscope; you should be able to visualize the vescicle fusion and serotonin release.
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