وأيد هذا العمل من قبل المعاهد الوطنية بتمويل من المنح الصحة 1R21NS073097-01 و1R01DK082884 (JSD) ومؤسسة PIER11VCTR الوطنية منحة المعاهد.

<ol>
	<li>Ehrlich, J. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inward+rectifier+potassium+currents+as+a+target+for+atrial+fibrillation+therapy.">Inward rectifier potassium currents as a target for atrial fibrillation therapy.</a> J. Cardiovasc. Pharmacol. 52 (2), 129 (2008).</li><li>Bhave, G., Lonergan, D., Chauder, B. A., Denton, J. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Small-molecule+modulators+of+inward+rectifier+K++channels:+recent+advances+and+future+possibilities.">Small-molecule modulators of inward rectifier K+ channels: recent advances and future possibilities.</a> Future Med. Chem. 2 (5), 757 (2010).</li><li>Swartz, K. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tarantula+toxins+interacting+with+voltage+sensors+in+potassium+channels.">Tarantula toxins interacting with voltage sensors in potassium channels.</a> Toxicon. 49 (2), 213 (2007).</li><li>Jin, W., Lu, Z. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+novel+high-affinity+inhibitor+for+inward-rectifier+K++channels.">A novel high-affinity inhibitor for inward-rectifier K+ channels.</a> Biochemistry. 37 (38), 13291 (1998).</li><li>Jin, W., Lu, Z. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Synthesis+of+a+stable+form+of+tertiapin:+a+high-affinity+inhibitor+for+inward-rectifier+K++channels.">Synthesis of a stable form of tertiapin: a high-affinity inhibitor for inward-rectifier K+ channels.</a> Biochemistry. 38 (43), 14286 (1999).</li><li>Roy, A., McDonald, P. R., Sittampalam, S., Chaguturu, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Open+access+high+throughput+drug+discovery+in+the+public+domain:+a+Mount+Everest+in+the+making.">Open access high throughput drug discovery in the public domain: a Mount Everest in the making.</a> Curr. Pharm. Biotechnol. 11 (7), 764 (2010).</li><li>Weaver, C. D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+thallium-sensitive,+fluorescence-based+assay+for+detecting+and+characterizing+potassium+channel+modulators+in+mammalian+cells.">A thallium-sensitive, fluorescence-based assay for detecting and characterizing potassium channel modulators in mammalian cells.</a> J. Biomol. Screen. 9 (8), 671 (2004).</li><li>Lewis, L. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High-throughput+screening+reveals+a+small-molecule+inhibitor+of+the+renal+outer+medullary+potassium+channel+and.">High-throughput screening reveals a small-molecule inhibitor of the renal outer medullary potassium channel and.</a> 76 (5), 1094 (2009).</li><li>Bhave, G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Development+of+a+selective+small-molecule+inhibitor+of+Kir1.1,+the+renal+outer+medullary+potassium+channel.">Development of a selective small-molecule inhibitor of Kir1.1, the renal outer medullary potassium channel.</a> Mol. Pharmacol. 79 (1), 42 (2011).</li><li>Raphemot, R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Discovery,+characterization,+and+structure-activity+relationships+of+an+inhibitor+of+inward+rectifier+potassium+(Kir)+channels+with+preference+for+Kir2.3,+Kir3.x,+and+Kir7.1.">Discovery, characterization, and structure-activity relationships of an inhibitor of inward rectifier potassium (Kir) channels with preference for Kir2.3, Kir3.x, and Kir7.1.</a> Front Pharmacol. 2, 75 (2012).</li><li>Niswender, C. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+novel+assay+of+Gi/o-linked+G+protein-coupled+receptor+coupling+to+potassium+channels+provides+new+insights+into+the+pharmacology+of+the+group+III+metabotropic+glutamate+receptors.">A novel assay of Gi/o-linked G protein-coupled receptor coupling to potassium channels provides new insights into the pharmacology of the group III metabotropic glutamate receptors.</a> Mol. Pharmacol. 73 (4), 1213 (2008).</li></ol>

الإعلان عن أي تضارب في المصالح.

بيانات العلاج: حالما يتم جمع البيانات، وهي خطوة مشتركة في التحليل ينطوي على تطبيع استجابة كل بئر في مضان، F، إلى قيمته الأولية في بداية التجربة، F 0. ويشار إلى هذه على أنها &quot;نسبة ثابتة&quot; ويرمز &quot;F / F 0&quot;. وفي الحالات التي يهيمن F 0 من ?...

An erratum was issued for: <a href="https://www.jove.com/video/4209/high-throughput-screening-for-small-molecule-modulators-inward">High-throughput Screening for Small-molecule Modulators of Inward Rectifier Potassium Channels</a>. The Protocol section has been updated.
The formula in step 7.1 of the Protocol has been updated from:
Z prime = 1- (3SDp + 3SDn)/|meanp + meann |
to:
Z prime = 1- (3SDp + 3SDn)/|meanp - meann |

An erratum was issued for: <a href="https://www.jove.com/video/4209/high-throughput-screening-for-small-molecule-modulators-inward">High-throughput Screening for Small-molecule Modulators of Inward Rectifier Potassium Channels</a>. The Protocol section has been updated.

Erratum: High-throughput Screening for Small-molecule Modulators of Inward Rectifier Potassium Channels

<table border="1" style=";text-align:right;direction:rtl"><tbody><tr><td> اسم كاشف </td><td> شركة </td><td> كتالوج رقم </td><td> تعليقات </td></tr><tr><td> pcDNA5/TO </td><td> إينفيتروجن </td><td> V1033-20 </td><td> التتراسيكلين-محرض التعبير ناقلات </td></tr><tr><td> T-REX-HEK293 الخلايا </td><td> إينفيتروجن </td><td> R71007 </td><td> التتراسيكلين-محرض خلية خط </td></tr><tr><td> Lipofectamine LTX / زائد الكاشف </td><td> إينفيتروجن </td><td> 15338100 </td><td> كاشف ترنسفكأيشن </td></tr><tr><td> FBS </td><td> ATLANTA الحيوية </td><td> S11550 </td><td> وسائل الإعلام خلية ثقافة </td></tr><tr><td> DMEM </td><td> إينفيتروجن </td><td> 11965 </td><td> وسائل الإعلام خلية ثقافة </td></tr><tr><td> هيغروميسين B </td><td> إينفيتروجن </td><td> 10687-010 </td><td> وسائل الإعلام خلية ثقافة </td></tr><tr><td> Blasticidin S </td><td> إينفيتروجن </td&gt; <td> R210-01 </td><td> وسائل الإعلام خلية ثقافة </td></tr><tr><td> البنسلين / الستربتوميسين </td><td> إينفيتروجن </td><td> 15140 </td><td> وسائل الإعلام خلية ثقافة </td></tr><tr><td> HBSS-ثنائي التكافؤ مجانا </td><td> Mediatech </td><td> 21022CV </td><td> خلية الغسيل </td></tr><tr><td> التربسين-0.25٪ </td><td> Mediatech </td><td> 25053CI </td><td> خلية التفكك </td></tr><tr><td> التتراسيكلين، حمض الهيدروكلوريك </td><td> سيجما </td><td> T9823 </td><td> الحث كاشف </td></tr><tr><td> مدال FBS </td><td> ATLANTA الحيوية </td><td> S12650 </td><td> الطلاء وسائل الإعلام </td></tr><tr><td> FluoZin-2 </td><td> إينفيتروجن </td><td> F24189 </td><td> صبغ فلوري </td></tr><tr><td> بلورونيك F-127 </td><td> إينفيتروجن </td><td> P-3000MP </td><td> صبغة التحميل </td></tr><tr><td> HBSS </td><td> إينفيتروجن </td><td> 14175 </td><td> مقايسة العازلة </td></tr><tr><td> HEPES </td><td> إينفيتروجن </td><td> 15630 </td><td> مقايسة العازلة </td></tr><tr><td> NaHCO 3 </td><td> سيجما </td><td> S6297 </td><td> TL + التحفيز العازلة </td></tr><tr><td> MgSO 4 </td><td> سيجما </td><td> M2643 </td><td> TL + التحفيز العازلة </td></tr><tr><td> كاسو 4 • 2H 2 O </td><td> سيجما </td><td> C3771 </td><td> TL + التحفيز العازلة </td></tr><tr><td> D-غلوكوز </td><td> سيجما </td><td> G7528 </td><td> TL + التحفيز العازلة </td></tr><tr><td> كبريتات الثاليوم </td><td> الدريتش </td><td> 204625 </td><td> TL + التحفيز العازلة </td></tr><tr><td> HEPES </td><td> سيجما </td><td> H4034 </td><td> TL + التحفيز العازلة </td></tr><tr><td> DMSO </td><td> سيجما </td><td> D4540 </td><td> مذيب </td></tr><tr><td> ثماني قنوات إلكترونية pipettor </td><td> Biohit </td><td> E300 </td><td> الطلاء الخلية في 384 -وحات جيدة </td></tr><tr><td> BD PureCoat أمين المغلفة 384 وحات جيدة </td><td> BD العلوم البيولوجية </td><td> 356719 </td><td> مقايسة microplates </td></tr><tr><td> تأهل صدى حسنا البولي بروبلين 384 صفيحة ميكروسكوبية (384PP) </td><td> Labcyte </td><td> P-05525 </td><td> microplates مجمع مصدر </td></tr><tr><td> microplates البولي بروبلين 384 جيد </td><td> غرينر بيو واحد </td><td> 781280 </td><td></td></tr><tr><td> Multidrop موزع كومبي كاشف </td><td> الحرارية العلمية </td><td> 5840300 </td><td></td></tr><tr><td> ELx405 صفيحة ميكروسكوبية غسالة </td><td> بيوتيك </td><td> ELx405HT </td><td> غسل الخلايا الآلي </td></tr><tr><td> صدى معالج السائل </td><td> Labcyte </td><td> Labcyte صدى 550 </td><td></td></tr><tr><td> برافو الآلي منصة تداول السائل </td><td> اجيلنت تكنولوجيز </td><td> نموذج قياسي </td><td></td></tr><tr><td> حمامةتسو FDSS 6000 </td><td> هاماماتسو </td><td></td><td> التصوير الحركي لوحة قارئ </td></tr></tbody></table> الجدول 1. قائمة المواد والكواشف.

high-throughput screening for small-molecule modulators of inward rectifier potassium channels

وافترض أعضاء معينة من البوتاسيوم المعدل الداخل الأسرة قناة (قير) أهداف المخدرات لمجموعة متنوعة من الاضطرابات، بما في ذلك ارتفاع ضغط الدم، الرجفان الأذيني، و1،2 الألم. بالنسبة للجزء الأكبر، ومع ذلك، فقد تم التقدم تباطأ نحو فهم إمكاناتها العلاجية أو الوظائف الفسيولوجية الأساسية حتى لعدم وجود أدوات الدوائية جيدة. في الواقع، وتأخر في علم الصيدلة الجزيئية الأسرة المعدل الداخل بعيدا وراء ذلك من الفصيلة S4 من الجهد بوابات قنوات (كيلو فولت) البوتاسيوم، والتي تم اكتشافها في عدد من تقارب-nanomolar وانتقائية للغاية جهري السم الببتيد 3. السم سم النحل tertiapin ومشتقاته ومثبطات قوية من Kir1.1 وKir3 قنوات 4،5، ولكن الببتيدات ذات الاستخدام المحدود علاجية وكذلك تجريبيا نظرا لخصائص المستضدية والتوافر البيولوجي الفقراء والاستقرار الأيضية وانتفاذ الأنسجة. تطوير قويةوسوف انتقائية الصغيرة جزيء تحقيقات مع تحسين الخصائص الدوائية تكون مفتاحا لفهم علم وظائف الأعضاء بشكل كامل والإمكانات العلاجية من القنوات قير. الجزيئية إنتاج مجسات مكتبات مركز شبكة (MLPCN) بدعم من المعاهد الوطنية للصحة (NIH) قد خلق فرص الصندوق المشترك للعلماء الأكاديمية لبدء التحقيق حملات اكتشاف الجزيئية للأهداف ومسارات الإشارات في حاجة إلى أفضل الصيدلة 6. ويقدم الباحثون MLPCN الوصول إلى مراكز الفرز الصناعة على نطاق والكيمياء الطبية والمعلوماتية دعم لتطوير جزيء صغير تحقيقات لتوضيح وظيفة الجينات وشبكات الجينات. الخطوة الحاسمة في كسب الدخول إلى MLPCN هو وضع مقايسة المستهدفة أو مسار محدد، قوية قابلة للالفرز الفائق الإنتاجية (HTS). هنا، نحن تصف كيفية تطوير مضان القائم على الثاليوم (TL +) تدفق أساذ وظيفة قناة قير للفحص مجمع عالية الإنتاجية 7،8،9،10. ويستند الفحص على نفاذية K + قناة المسام ليرة تركية K + + متجانس. ويستخدم الفلورسنت المتاحة تجاريا ثاليوم + مراسل صبغ للكشف عن تدفق عبر الغشاء من ثاليوم + من خلال المسام. هناك على الأقل ثلاثة الأصباغ المتاحة تجاريا التي هي مناسبة لفحوصات + ثاليوم تدفق: BTC، FluoZin-2، 7،8 وFluxOR. يصف هذا البروتوكول باستخدام مقايسة التنمية FluoZin-2. على الرغم من أن وضعت أصلا وتسويقها كمؤشر الزنك، FluoZin-2 المعروضات زيادة جرعة قوية وتعتمد على الانبعاثات في مضان على ثاليوم + ملزمة. بدأنا العمل مع FluoZin-2 قبل FluxOR كانت متاحة 7،8 واستمرت في القيام بذلك 9،10. ومع ذلك، فإن الخطوات في تطوير الفحص متطابقة أساسا لجميع الأصباغ الثلاثة، ويجب على المستخدمين تحديد أي صبغة هي الأنسب لن الخاصةeeds. نناقش أيضا مقاييس أداء الفحص أنه يجب التوصل للنظر في الدخول إلى MLPCN. منذ ثاليوم + يتخلل بسهولة أكثر K + قنوات، ينبغي أن تكون قابلة للتكيف مع مقايسة الأهداف الأكثر K + القناة.

استخدام نظام التعبير التتراسيكلين-محرض يوفر عنصر تحكم مريحة الداخلية للتمييز ثاليوم + تدفق من خلال مسارات الذاتية وقناة قير للاهتمام. الشكل 1 يبين بعض الأمثلة من الخرائط المستخدمة في الطلاء الخلية أنواع مختلفة من التجارب. يشار إلى مواقف الآبار التي تح...

Watch this Scientific Journal Video about High-throughput Screening for Small-molecule Modulators of Inward Rectifier Potassium Channels at JoVE.com

High-throughput Screening for Small-molecule Modulators of Inward Rectifier Potassium Channels

يتم تقديم أساليب لتطوير والتحقق من صحة مقايسة الكمية مضان لقياس نشاط البوتاسيوم المعدل الداخل (قير) قنوات لفحص المجمع الإنتاجية العالية.

الفرز الفائق الإنتاجية الصغيرة للجزيء المغيرون من الداخل قنوات البوتاسيوم المعدل

Specific members of the inward rectifier potassium (Kir) channel family are postulated drug targets for a variety of disorders, including hypertension, ...

high-throughput-screening-for-small-molecule-modulators-inward

Research

JoVE Journal

Biology

14.9K Views.  Vanderbilt University School of Medicine. يتم تقديم أساليب لتطوير والتحقق من صحة مقايسة الكمية مضان لقياس نشاط البوتاسيوم المعدل الداخل (قير) قنوات لفحص المجمع الإنتاجية العالية.

Video: High-throughput Screening for Small-molecule Modulators of Inward Rectifier Potassium Channels

High-throughput Screening and Biosensing with Fluorescent C. elegans Strains

High-throughput screening (HTS) is a powerful approach for identifying chemical modulators of biological processes. However, many compounds identified in screens using cell culture models are often found to be toxic or pharmacologically inactive in vivo1-2. Screening in whole animal models can help avoid these pitfalls and streamline the path to drug development.
C. elegans is a multicellular model organism well suited for HTS. It is small (&lt;1 mm) and can be economically cultured and dispensed in liquids. C. elegans is also one of the most experimentally tractable animal models permitting rapid and detailed identification of drug mode-of-action3.
We describe a protocol for culturing and dispensing fluorescent strains of C. elegans for high-throughput screening of chemical libraries or detection of environmental contaminants that alter the expression of a specific gene. Large numbers of developmentally synchronized worms are grown in liquid culture, harvested, washed, and suspended at a defined density. Worms are then added to black, flat-bottomed 384-well plates using a peristaltic liquid dispenser. Small molecules from a chemical library or test samples (e.g., water, food, or soil) can be added to wells with worms. In vivo, real-time fluorescence intensity is measured with a fluorescence microplate reader. This method can be adapted to any inducible gene in C. elegans for which a suitable reporter is available. Many inducible stress and developmental transcriptional pathways are well defined in C. elegans and GFP transgenic reporter strains already exist for many of them4. When combined with the appropriate transgenic reporters, our method can be used to screen for pathway modulators or to develop robust biosensor assays for environmental contaminants. 
We demonstrate our C. elegans culture and dispensing protocol with an HTS assay we developed to monitor the C. elegans cap &#x2018;n&#x2019; collar transcription factor SKN-1. SKN-1 and its mammalian homologue Nrf2 activate cytoprotective genes during oxidative and xenobiotic stress5-10. Nrf2 protects mammals from numerous age-related disorders such as cancer, neurodegeneration, and chronic inflammation and has become a major chemotherapeutic target11-13.Our assay is based on a GFP transgenic reporter for the SKN-1 target gene gst-414, which encodes a glutathione-s transferase6. The gst-4 reporter is also a biosensor for xenobiotic and oxidative chemicals that activate SKN-1 and can be used to detect low levels of contaminants such as acrylamide and methyl-mercury15-16.

High-throughput Screening and Biosensing with Fluorescent C. elegans Strains

A procedure for liquid-based culturing and dispensing of C. elegans strains expressing fluorescent reporter proteins is described that does not require expensive sorting equipment. This approach can be applied to numerous inducible C. elegans genes for drug discovery or biosensing of contaminants.

الفرز الفائق الإنتاجية وBiosensing مع نيون C. ايليجانس سلالات

High-throughput screening (HTS) is a powerful approach for identifying chemical modulators of biological processes.  However, many compounds identified in ...

High Throughput Screening of Fungal Endoglucanase Activity in Escherichia coli

Cellulase enzymes (endoglucanases, cellobiohydrolases, and &beta;-glucosidases) hydrolyze cellulose into component sugars, which in turn can be converted into fuel alcohols1. The potential for enzymatic hydrolysis of cellulosic biomass to provide renewable energy has intensified efforts to engineer cellulases for economical fuel production2. Of particular interest are fungal cellulases3-8, which are already being used industrially for foods and textiles processing.
Identifying active variants among a library of mutant cellulases is critical to the engineering process; active mutants can be further tested for improved properties and/or subjected to additional mutagenesis. Efficient engineering of fungal cellulases has been hampered by a lack of genetic tools for native organisms and by difficulties in expressing the enzymes in heterologous hosts. Recently, Morikawa and coworkers developed a method for expressing in E. coli the catalytic domains of endoglucanases from H. jecorina3,9, an important industrial fungus with the capacity to secrete cellulases in large quantities. Functional E. coli expression has also been reported for cellulases from other fungi, including Macrophomina phaseolina10 and Phanerochaete chrysosporium11-12. 
We present a method for high throughput screening of fungal endoglucanase activity in E. coli. (Fig 1) This method uses the common microbial dye Congo Red (CR) to visualize enzymatic degradation of carboxymethyl cellulose (CMC) by cells growing on solid medium. The activity assay requires inexpensive reagents, minimal manipulation, and gives unambiguous results as zones of degradation (&#x201C;halos&#x201D;) at the colony site. Although a quantitative measure of enzymatic activity cannot be determined by this method, we have found that halo size correlates with total enzymatic activity in the cell. Further characterization of individual positive clones will determine , relative protein fitness. 
Traditional bacterial whole cell CMC/CR activity assays13 involve pouring agar containing CMC onto colonies, which is subject to cross-contamination, or incubating cultures in CMC agar wells, which is less amenable to large-scale experimentation. Here we report an improved protocol that modifies existing wash methods14 for cellulase activity: cells grown on CMC agar plates are removed prior to CR staining. Our protocol significantly reduces cross-contamination and is highly scalable, allowing the rapid screening of thousands of clones. In addition to H. jecorina enzymes, we have expressed and screened endoglucanase variants from the Thermoascus aurantiacus and Penicillium decumbens (shown in Figure 2), suggesting that this protocol is applicable to enzymes from a range of organisms.

High Throughput Screening of Fungal Endoglucanase Activity in Escherichia coli

We describe a low cost, high throughput method to screen for fungal endoglucanase activity in E. coli. The method relies on a simple visual readout of substrate degradation, does not require enzyme purification, and is highly scalable. This allows for the rapid screening of large libraries of enzyme variants.

ارتفاع المناولة فحص النشاط Endoglucanase الفطرية في القولونية</em

Cellulase enzymes (endoglucanases, cellobiohydrolases, and &beta;-glucosidases) hydrolyze cellulose into component sugars, which in turn can be converted ...

A Fluorescent Screening Assay for Identifying Modulators of GIRK Channels

G protein-gated inward rectifier K+ (GIRK) channels function as cellular mediators of a wide range of hormones and neurotransmitters and are expressed in the brain, heart, skeletal muscle and endocrine tissue1,2. GIRK channels become activated following the binding of ligands (neurotransmitters, hormones, drugs, etc.) to their plasma membrane-bound, G protein-coupled receptors (GPCRs). This binding causes the stimulation of G proteins (Gi and Go) which subsequently bind to and activate the GIRK channel. Once opened the GIRK channel allows the movement of K+ out of the cell causing the resting membrane potential to become more negative. As a consequence, GIRK channel activation in neurons decreases spontaneous action potential formation and inhibits the release of excitatory neurotransmitters. In the heart, activation of the GIRK channel inhibits pacemaker activity thereby slowing the heart rate.
GIRK channels represent novel targets for the development of new therapeutic agents for the treatment neuropathic pain, drug addiction, cardiac arrhythmias and other disorders3. However, the pharmacology of these channels remains largely unexplored. Although a number of drugs including anti-arrhythmic agents, antipsychotic drugs and antidepressants block the GIRK channel, this inhibition is not selective and occurs at relatively high drug concentrations3.
Here, we describe a real-time screening assay for identifying new modulators of GIRK channels. In this assay, neuronal AtT20 cells, expressing GIRK channels, are loaded with membrane potential-sensitive fluorescent dyes such as bis-(1,3-dibutylbarbituric acid) trimethine oxonol [DiBAC4(3)] or HLB 021-152 (Figure 1). The dye molecules become strongly fluorescent following uptake into the cells (Figure 1). Treatment of the cells with GPCR ligands stimulates the GIRK channels to open. The resulting K+ efflux out of the cell causes the membrane potential to become more negative and the fluorescent signal to decrease (Figure 1). Thus, drugs that modulate K+ efflux through the GIRK channel can be assayed using a fluorescent plate reader. Unlike other ion channel screening assays, such atomic absorption spectrometry4 or radiotracer analysis5, the GIRK channel fluorescent assay provides a fast, real-time and inexpensive screening procedure.

A real-time screening procedure for identifying drugs that interact with G protein-gated inward rectifier K+ (GIRK) channels is described. The assay utilizes membrane potential-sensitive fluorescent dyes to measure GIRK channel activity. This technique is adaptable for use on a number of cell lines.

والفحص الفحص نيون لتحديد المغيرون من القنوات GIRK

G protein-gated inward rectifier K+ (GIRK) channels function as cellular mediators of a wide range of hormones and neurotransmitters and are expressed in ...

High-throughput Functional Screening using a Homemade Dual-glow Luciferase Assay

We present a rapid and inexpensive high-throughput screening protocol to identify transcriptional regulators of alpha-synuclein, a gene associated with Parkinson&#39;s disease. 293T cells are transiently transfected with plasmids from an arrayed ORF expression library, together with luciferase reporter plasmids, in a one-gene-per-well microplate format. Firefly luciferase activity is assayed after 48 hr to determine the effects of each library gene upon alpha-synuclein transcription, normalized to expression from an internal control construct (a hCMV promoter directing Renilla luciferase). This protocol is facilitated by a bench-top robot enclosed in a biosafety cabinet, which performs aseptic liquid handling in 96-well format. Our automated transfection protocol is readily adaptable to high-throughput lentiviral library production or other functional screening protocols requiring triple-transfections of large numbers of unique library plasmids in conjunction with a common set of helper plasmids. We also present an inexpensive and validated alternative to commercially-available, dual luciferase reagents which employs PTC124, EDTA, and pyrophosphate to suppress firefly luciferase activity prior to measurement of Renilla luciferase. Using these methods, we screened 7,670 human genes and identified 68 regulators of alpha-synuclein. This protocol is easily modifiable to target other genes of interest.

We present a rapid and inexpensive screening method for identifying transcriptional regulators using high-throughput robotic transfections and a homemade dual-glow luciferase assay. This protocol rapidly generates direct side-by-side functional data for thousands of genes and is easily modifiable to target any gene of interest.

الإنتاجية العالية فحص وظيفية باستخدام محلية الصنع ثنائي توهج luciferase الفحص

We present a rapid and inexpensive high-throughput screening protocol to identify transcriptional regulators of alpha-synuclein, a gene associated with ...

A Method of Permeabilization of Drosophila Embryos for Assays of Small Molecule Activity

The Drosophila embryo has long been a powerful laboratory model for elucidating molecular and genetic mechanisms that control development. The ease of genetic manipulations with this model has supplanted pharmacological approaches that are commonplace in other animal models and cell-based assays. Here we describe recent advances in a protocol that enables application of small molecules to the developing fruit fly embryo. The method details steps to overcome the impermeability of the eggshell while maintaining embryo viability. Eggshell permeabilization across a broad range of developmental stages is achieved by application of a previously described d-limonene embryo permeabilization solvent (EPS1) and by aging embryos at reduced temperature (18 &#176;C) prior to treatments. In addition, use of a far-red dye (CY5) as a permeabilization indicator is described, which is compatible with downstream applications involving standard red and green fluorescent dyes in live and fixed preparations. This protocol is applicable to studies using bioactive compounds to probe developmental mechanisms as well as for studies aimed at evaluating teratogenic or pharmacologic activity of uncharacterized small molecules.

A Method of Permeabilization of Drosophila Embryos for Assays of Small Molecule Activity

Introduction of small molecules to the developing Drosophila embryo offers great potential for characterizing biological activity of novel compounds, drugs, and toxins as well as for probing fundamental developmental pathways. Methods described herein outline steps that overcome natural barriers to this approach, expanding the utility of the Drosophila embryo model.

A طريقة Permeabilization من<em&gt; ذبابة الفاكهة</em&gt; الأجنة للفحوصات الصغيرة جزيء آخر

The Drosophila embryo has long been a powerful laboratory model for elucidating molecular and genetic mechanisms that control development. The ease of ...

A Manual Small Molecule Screen Approaching High-throughput Using Zebrafish Embryos

Zebrafish have become a widely used model organism to investigate the mechanisms that underlie developmental biology and to study human disease pathology due to their considerable degree of genetic conservation with humans. Chemical genetics entails testing the effect that small molecules have on a biological process and is becoming a popular translational research method to identify therapeutic compounds. Zebrafish are specifically appealing to use for chemical genetics because of their ability to produce large clutches of transparent embryos, which are externally fertilized. Furthermore, zebrafish embryos can be easily drug treated by the simple addition of a compound to the embryo media. Using whole-mount in situ hybridization (WISH), mRNA expression can be clearly visualized within zebrafish embryos. Together, using chemical genetics and WISH, the zebrafish becomes a potent whole organism context in which to determine the cellular and physiological effects of small molecules. Innovative advances have been made in technologies that utilize machine-based screening procedures, however for many labs such options are not accessible or remain cost-prohibitive. The protocol described here explains how to execute a manual high-throughput chemical genetic screen that requires basic resources and can be accomplished by a single individual or small team in an efficient period of time. Thus, this protocol provides a feasible strategy that can be implemented by research groups to perform chemical genetics in zebrafish, which can be useful for gaining fundamental insights into developmental processes, disease mechanisms, and to identify novel compounds and signaling pathways that have medically relevant applications.

The zebrafish is an excellent experimental organism to study vertebrate developmental processes and model human disease. Here, we describe a protocol on how to perform a manual high-throughput chemical screen in zebrafish embryos with a whole-mount in situ hybridization (WISH) read-out.

دليل جزيء صغير شاشة تقترب عالية الإنتاجية عن طريق الزرد الأجنة

Zebrafish have become a widely used model organism to investigate the mechanisms that underlie developmental biology and to study human disease pathology ...

High-throughput Screening for Chemical Modulators of Post-transcriptionally Regulated Genes

Both transcriptional and post-transcriptional regulation have a profound impact on genes expression. However, commonly adopted cell-based screening assays focus on transcriptional regulation, being essentially aimed at the identification of promoter-targeting molecules. As a result, post-transcriptional mechanisms are largely uncovered by gene expression targeted drug development. Here we describe a cell-based assay aimed at investigating the role of the 3&#39; untranslated region (3&#8217; UTR) in the modulation of the fate of its mRNA, and at identifying compounds able to modify it. The assay is based on the use of a luciferase reporter construct containing the 3&#8217; UTR of a gene of interest stably integrated into a disease-relevant cell line. The protocol is divided into two parts, with the initial focus on the primary screening aimed at the identification of molecules affecting luciferase activity after 24 hr of treatment. The second part of the protocol describes the counter-screening necessary to discriminate compounds modulating luciferase activity specifically through the 3&#8217; UTR. In addition to the detailed protocol and representative results, we provide important considerations about the assay development and the validation of the hit(s) on the endogenous target. The described cell-based reporter gene assay will allow scientists to identify molecules modulating protein levels via post-transcriptional mechanisms dependent on a 3&#8217; UTR.

Here we describe a cell-based reporter gene assay as a valuable tool to screen chemical libraries for compounds modulating post-transcriptional control mechanisms exerted through 3&#8217; UTR.

الإنتاجية العالية للكشف عن المغيرون الكيميائية من الجينات المشاركة ما بعد transcriptionally الخاضعة للرقابة

Both transcriptional and post-transcriptional regulation have a profound impact on genes expression. However, commonly adopted cell-based screening assays ...

Identification of Kinase-substrate Pairs Using High Throughput Screening

We have developed a screening platform to identify dedicated human protein kinases for phosphorylated substrates which can be used to elucidate novel signal transduction pathways. Our approach features the use of a library of purified GST-tagged human protein kinases and a recombinant protein substrate of interest. We have used this technology to identify MAP/microtubule affinity-regulating kinase 2 (MARK2) as the kinase for a glucose-regulated site on CREB-Regulated Transcriptional Coactivator 2 (CRTC2), a protein required for beta cell proliferation, as well as the Axl family of tyrosine kinases as regulators of cell metastasis by phosphorylation of the adaptor protein ELMO. We describe this technology and discuss how it can help to establish a comprehensive map of how cells respond to environmental stimuli.

Protein phosphorylation is a central feature of how cells interpret and respond to information in their extracellular milieu. Here, we present a high throughput screening protocol using kinases purified from mammalian cells to rapidly identify kinases that phosphorylate a substrate(s) of interest.

تحديد أزواج كيناز الركيزة عن طريق فحص إنتاجية عالية


We have developed a screening platform to identify dedicated human protein kinases for phosphorylated substrates which can be used to elucidate novel ...

Automated Modular High Throughput Exopolysaccharide Screening Platform Coupled with Highly Sensitive Carbohydrate Fingerprint Analysis

Many microorganisms are capable of producing and secreting exopolysaccharides (EPS), which have important implications in medical fields, food applications or in the replacement of petro-based chemicals. We describe an analytical platform to be automated on a liquid handling system that allows the fast and reliable analysis of the type and the amount of EPS produced by microorganisms. It enables the user to identify novel natural microbial exopolysaccharide producers and to analyze the carbohydrate fingerprint of the corresponding polymers within one day in high-throughput (HT). Using this platform, strain collections as well as libraries of strain variants that might be obtained in engineering approaches can be screened. The platform has a modular setup, which allows a separation of the protocol into two major parts. First, there is an automated screening system, which combines different polysaccharide detection modules: a semi-quantitative analysis of viscosity formation via a centrifugation step, an analysis of polymer formation via alcohol precipitation and the determination of the total carbohydrate content via a phenol-sulfuric-acid transformation. Here, it is possible to screen up to 384 strains per run. The second part provides a detailed monosaccharide analysis for all the selected EPS producers identified in the first part by combining two essential modules: the analysis of the complete monomer composition via ultra-high performance liquid chromatography coupled with ultra violet and electrospray ionization ion trap detection (UHPLC-UV-ESI-MS) and the determination of pyruvate as a polymer substituent (presence of pyruvate ketal) via enzymatic oxidation that is coupled to a color formation. All the analytical modules of this screening platform can be combined in different ways and adjusted to individual requirements. Additionally, they can all be handled manually or performed with a liquid handling system. Thereby, the screening platform enables a huge flexibility in order to identify various EPS.

We present an automated modular high-throughput-method for the identification and characterization of microbial exopolysaccharides in small scale. This method combines a fast preselection to analyze the total amount of secreted polysaccharides with a detailed carbohydrate fingerprint to enable the fast screening of newly isolated bacterial strains or entire strain collections.

الآلي وحدات إنتاجية عالية Exopolysaccharide فحص منصة مقرونا حساسة للغاية تحليل الكربوهيدرات بصمات الأصابع

Many microorganisms are capable of producing and secreting exopolysaccharides (EPS), which have important implications in medical fields, food ...

Multi-enzyme Screening Using a High-throughput Genetic Enzyme Screening System

The recent development of a high-throughput single-cell assay technique enables the screening of novel enzymes based on functional activities from a large-scale metagenomic library1. We previously proposed a genetic enzyme screening system (GESS) that uses dimethylphenol regulator activated by phenol or p-nitrophenol. Since a vast amount of natural enzymatic reactions produce these phenolic compounds from phenol deriving substrates, this single genetic screening system can be theoretically applied to screen over 200 different enzymes in the BRENDA database. Despite the general applicability of GESS, applying the screening process requires a specific procedure to reach the maximum flow cytometry signals. Here, we detail the developed screening process, which includes metagenome preprocessing with GESS and the operation of a flow cytometry sorter. Three different phenolic substrates (p-nitrophenyl acetate, p-nitrophenyl-&#946;-D-cellobioside, and phenyl phosphate) with GESS were used to screen and to identify three different enzymes (lipase, cellulase, and alkaline phosphatase), respectively. The selected metagenomic enzyme activities were confirmed only with the flow cytometry but DNA sequencing and diverse in vitro analysis can be used for further gene identification.

This work presents a method of high-throughput screening using a universal genetic enzyme screening system that can be theoretically applied to over 200 enzymes. Here, the single screening system identifies three different enzymes (lipase, cellulase, and alkaline phosphatase) by simply changing the substrate used (p-nitrophenyl acetate, p-nitrophenyl-&#946;-D-cellobioside, and phenyl phosphate).

متعدد انزيم الفحص باستخدام عالية الإنتاجية نظام فحص انزيم الوراثية

The recent development of a high-throughput single-cell assay technique enables the screening of novel enzymes based on functional activities from a ...