Bu çalışma Luminex Corporation tarafından finanse edildi.

<ol>
	<li>Fulton, J. R., McDade, R. L., Smith, P. L., Kienker, L. J., Kettman, 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=Advanced+multiplexed+analysis+with+the+FlowMetrix+system.">Advanced multiplexed analysis with the FlowMetrix system.</a> Clinical Chemistry. 43, 1749-1756 (1997).</li><li>Carson, R. T., Vignali, A. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Simultaneous+quantation+of+15+cytokines+using+a+multiplexed+flow+cytometric+assay.">Simultaneous quantation of 15 cytokines using a multiplexed flow cytometric assay.</a> J. Immunol. Methods. 227, 41-52 (1999).</li><li>Peck, D., Crawford, E. D., Ross, K. N., Stegmaier, K., Golub, T. R., Lamb, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+method+for+high-throughput+gene+expression+signature+analysis.">A method for high-throughput gene expression signature analysis.</a> Genome Biol. 7, 61 (2006).</li><li>VanDerMeid, K. R., Su, S. P., Krenzer, K. L., Ward, K. W., Zhang, J. 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+method+to+extract+cytokines+and+matrix+metalloproteinases+from+Schirmer+strips+and+analyze+using+Luminex.">A method to extract cytokines and matrix metalloproteinases from Schirmer strips and analyze using Luminex.</a> Mol Vis. 17, 1056-1063 (2011).</li><li>Liu, J., Kibiki, G., Maro, V., Maro, A., Kumburu, H., Swai, N., Taniuchi, M., Gratz, J., Toney, D., Kang, G., Houpt, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Multiplex+reverse+transcription+PCR+Luminex+assay+for+detection+and+quantitation+of+viral+agents+of+gastroenteritis.">Multiplex reverse transcription PCR Luminex assay for detection and quantitation of viral agents of gastroenteritis.</a> J. Clin. Virol. 50, 308-313 (2011).</li><li>de Jager, W., Prakken, B. J., Bijlsma, J., WJ Kuis, W., Rijkers, G. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Improved+multiplex+immunoassay+performance+in+human+plasma+and+synovial+fluid+following+removal+of+interfering+heterophilic+antibodies.">Improved multiplex immunoassay performance in human plasma and synovial fluid following removal of interfering heterophilic antibodies.</a> J. Immunol. Methods. 300, 124-135 (2005).</li><li>Codorean, E., Nichita, C., Albulescu, L., Raducan, E., Popescu, I. D., Lonita, A. C., Albulescu, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Correlation+of+xMAP+and+ELISA+cytokine+profiles;+development+and+validation+for+immunotoxicological+studies+in+vitro.">Correlation of xMAP and ELISA cytokine profiles; development and validation for immunotoxicological studies in vitro.</a> Roum. Arch. Microbiol. Immunol. 69, 3-19 (2010).</li><li>de Jager, W., te Velthuis, H., Prakken, B. J., Kuis, W., Rijkers, G. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Simultaneous+detection+of+15+human+cytokines+in+a+single+sample+of+stimulated+peripheral+blood+mononuclear+cells.">Simultaneous detection of 15 human cytokines in a single sample of stimulated peripheral blood mononuclear cells.</a> Clin. Diagn. Lab. Immunol. 10, 133-139 (2003).</li><li>DuPont, N. C., Wang, K. H., Wadhwa, P. D., Culhane, J. F., Nelson, E. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Validation+and+comparison+of+Luminex+multiplex+cytokine+analysis+kits+with+ELISA:+Determinations+of+a+panel+of+nine+cytokines+in+clinical+sample+culture+supernatants.">Validation and comparison of Luminex multiplex cytokine analysis kits with ELISA: Determinations of a panel of nine cytokines in clinical sample culture supernatants.</a> J. Reprod. Immunol. 66, 175-191 (2005).</li><li>Richens, J. L., Urbanowicz, R. A., Metcalf, R., Corne, J., O'Shea, P., Fairclough, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantitative+validation+and+comparison+of+multiplex+cytokine+kits.">Quantitative validation and comparison of multiplex cytokine kits.</a> Journal of Biomolecular Screening. 15, 562-568 (2010).</li><li>Rizzi, G., Zhang, Y. J., Latek, R., Weiner, R., Rhyne, P. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Characterization+and+development+of+a+Luminex-based+assay+for+the+detection+of+human+IL-23.">Characterization and development of a Luminex-based assay for the detection of human IL-23.</a> Bioanalysis. 2, 1561-1572 (2010).</li></ol>

Bu çalışma Luminex Corporation üretilen ekipmanlar ile Luminex Corporation yapıldı. R &amp; D Systems &amp; EMD Millipore Luminex Corporation&#39;ın stratejik ortakları olan; multipleks xMAP dayalı testler geliştirmek ve ticarileştirmek için lisanslı.

Luminex xMAP platformuna bir ELISA testinin dönüşüm streptavidin fikoeritrin (SA-PE) ile tipik bir ELISA kiti streptavidin horseradish peroksidaz (SA-HRP) yerine, ve performans için optimize kadar basit olabilir. Kadar yerden bir xMAP immunoassay yaratmak isteyenler için, bu da antikor çiftlerinin hızlı, multipleks değerlendirilmesini sağlar basit bir protokol ile gerçekleştirilebilir. XMAP tayini için reaktifler kolayca çift belirlenmiş yakalama antikorlar MagPlex düşük konsantrasyonda mikrosferler ile xMAP Antikor Kuplaj kiti kullanılarak hazırlandı. Düşük konsantrasyonda mikrosferler kullanımı daha yüksek konsantrasyonda mikrosferler ile aynı test performansı sağlarken assay gelişme maliyetini düşürür. Birleştiğinde MagPlex mikrosferler hazırlamak için gerekli zaman miktarı olan 22 daha hızlıdır, yaklaşık 3 saat - 24 saat tedavi ardından, mont, bir ELISA plaka iyi için gereklikaplamalı kuyuların. XMAP testinin performanslı bir algılama (&lt;4 pg / mL vs&gt; 31 pg / mL) ve dinamik aralık (&lt;4 pg / ml&gt; 8000 pg / mL vs 16 sınırı açısından da ELISA üstündür pg / ml 1000 pg / ml). Plaka okuyucuların bir deney için dinamik aralığı üst sınırını kısıtlayarak, ya 3 ya da 4 OD sınırlı bir OD yelpazesi var. Kuşkusuz, tüm antikorların ELISA biçimde çalışır ve bir ELISA iyi çalışmamaktadır tüm antikorlar xMAP tahlil formata kolayca aktarılabilir. XMAP testler (aynı anda çalışabilir, yani) çoğaltılmış olabilir beri Ancak, bir deney için kullanılacak en iyi çifti belirlemek için aynı anda birden fazla yakalama ve algılama antikor kombinasyonları değerlendirmek mümkündür. Bu süreç, önemli zaman ve her seferinde bir çiftin değerlendirilmesi ile sınırlıdır ELISA geliştirme prosedürü göre reaktifleri kaydeder. Iki veya daha fazla antikor çiftleri eşdeğer yapmalıdır; testin diğer parametreleri olabilirçift ​​(örneğin, kullanılabilirlik, maliyet, vb) uygunluğunu belirlemek için düşünülebilir. XMAP tayini ile geliştirilmiş test performans ve esnekliğe ek olarak, önemli maliyet tasarrufları da vardır. Bir xMAP assay of iyi bir kullanılan boncuklar için gerekli miktarı yaklaşık 7.5 ng iken antikor tavsiye edilen miktarı, tek bir kat ve bir ELISA plaka 400ng olduğu için gereklidir. Böylece, bir ELISA için gerekli olan antikor miktarını iyi bir xMAP deneyde kullanılır ise, 50 den fazla test sonuçları sağlayacaktır. Değerli örnekleri içeren uygulamalar için, xMAP ayrıca önemli bir avantajı vardır. XMAP tahlil için gerekli hacminin yarısı veya daha az olabilir, oysa ELISA için önerilen örnek hacmi 100 uL olduğunu. Üstün dinamik aralık ve duyarlılık ile test üretirken Özetle, Luminex xMAP platformuna bir ELISA testinin dönüştürme, komplikasyonsuz verimli ve maliyet tasarrufu sağlar.

<table border="1"><tbody><tr><td> Tanım </td><td> Satıcı </td><td> Katalog Numarası </td><td> Yorumlar </td></tr><tr><td> İnsan TNF-α/TNFSF1A DuoSet ELISA kiti </td><td> R &amp; D Systems </td><td> DY210 </td><td> Monoklonal ve biyotin birleştiğinde poliklonal antikorlar ve rekombinant TNF-α standart protein içerir </td></tr><tr><td> TNF-α, monoklonal antikor </td><td> Abcam </td><td> Ab18696 </td><td> , Klon CH8820 Antikor Capture </td></tr><tr><td> TNF-α, monoklonal antikor </td><td> Abcam </td><td> Ab16166 </td><td> Biotin coupled Algılama Antikor, klon AS1 </td></tr><tr><td> TNF alfa protein </td><td> Abcam </td><td> Ab9642 </td><td> Rekombinant TNF-α protein standart </td></tr><tr><td> TNF-α, monoklonal antikor </td><td> Novus </td><td> NBP1-50115 </td><td> , Klon 4H31 Antikor Capture </td></tr><tr><td> TNF-α, monoklonal antikor </td><td> Novus </td><td> NB100-78.162 </td><td> Biotin coupled Algılama Antikor, klon MAb11 </td></tr><tr><td> TNF alfa protein </td><td> Novus </td><td> NBC1-18460 </td><td> Rekombinant TNF-α protein standart </td></tr><tr><td> TNF-α, monoklonal antikor </td><td> EMD Millipore </td><td> MAB1141 </td><td> Antikor Capture, 3C7.2 clone </td></tr><tr><td> TNF-α için poliklonal antikor </td><td> EMD Millipore </td><td> 654250 </td><td> Tavşan poliklonal Algılama Antikor </td></tr><tr><td> Streptavidin-Fikoeritrin </td><td> Yosun </td><td> SAPE-001 </td><td> Luminex xMAP Assay için Floresan muhabiri reaktif </td></tr><tr><td> MAGPIX w / xPONENT Yazılım </td><td> Luminex Şirketi </td><td> MAGPIX-XPONENT </td><td> Luminex Enstrüman </td></tr><tr><td> xMAP Antikor Kaplin (AbC) Kit </td><td> Luminex Şirketi </td><td> 40-50016 </td><td> EDC reaktifi, sülfo-NHS reaktifi aktivasyon tampon, yıkama tamponu, 1.5 ml reaksiyon tüpleri ve tek kullanımlık pipetler içerir </td></tr><tr><td> MagPlex mikroküreleri Düşük Konsantrasyon </td><td> Luminex Şirketi </td><td> MC10012-ID, MC10013-ID, MC10014-ID, MC10015-ID </td><td> Düşük konsantrasyon boncuklar (@ 2.5 x 10 6 boncuk / mL) </td></tr><tr><td> EZ-Link sülfo-NHS-LC-Biotin </td><td> Thermo Fisher </td><td> PI-21335 </td><td> Değiştirilmemiş algılama antikor biyotinilasyon kiti </td></tr><tr><td> Tecan Sonsuz F200 Okuyucu </td><td> Tecan </td><td></td><td> ELISA plaka okuyucu </td></tr><tr><td> Fosfat Tamponlu Salin </td><td> Sigma-Aldrich </td><td> P-3688 </td><td> % 1 BSA-PBS, Tayin tamponu </td></tr><tr><td> Bir Pint Kompakt Ultrasonik Temizleyici, 115 VAC </td><td> Cole-Parmer </td><td> WU-08.849-00 </td><td> 55 kHz etkili bir çalışma frekansı üretin </td></tr><tr><td> Manyetik Boru Ayırıcı </td><td> Luminex Şirketi </td><td> CN-0288-01 </td><td> Kaplin yıkama adımları tek 1.5mL tüp manyetik ayırma için </td></tr><tr><td> Manyetik Kalıp Ayırıcı </td><td> Luminex Şirketi </td><td> CN-0269-01 </td><td> Tahlil yıkama adımda 96-plaka manyetik ayırma için </td></tr></tbody></table>

conversion of a capture elisa to a luminex xmap assay using a multiplex antibody screening method

Enzim bağlı immünosorbent assay (ELISA) uzun yaşam bilim araştırma ve klinik teşhis hem de biyolojik örnekler ilgi analitlerin tespiti için temel araç olmuştur. Bununla birlikte, ELISA sınırlamaları vardır. Bu, tipik olarak bir 96-kuyucuklu mikroplaka gerçekleştirilir ve kuyuları, ilgilenilen bir antijen yakalamak için örnek nispeten büyük bir miktarda gerektiren, yakalama antikoru ile kaplanır. Kuyularının geniş yüzey alanına ve antikor çekimi hidrofobik bağlayıcı da spesifik olmayan bağlama ve yüksek arka yol açabilir. Ayrıca, çoğu ELISA&#39;lar makul bir hassasiyeti elde etmek için sinyallerin enzim-aracılı amplifikasyon dayanır. Böyle amplifikasyon her zaman doğrusal değildir ve can böylece çarpık sonuçlar. Geçen 15 yıl içinde, yeni bir teknoloji benzer bir wo ile, bu ELISA faydalar sunar, aynı zamanda daha yüksek verim, yüksek esneklik, azaltılmış örnek hacmi ve düşük maliyet sağlayan ortaya çıkmıştırrkflow 1, 2. Luminex xMAP Teknoloji monoplex protein ve nükleik asit uygulamalarının 3-5 hem uygulanabilir multipleks testler ile birlikte etkin bir mikroküre (boncuk) dizi platformudur. Boncuklar ELISA ile karşılaştırıldığında, daha az ve daha küçük antikor çekimi Örnek miktarlara, kovalent olarak daha küçük bir yüzey alanı üzerine sabitlenmiş yakalama antikoru sahiptir, ve spesifik olmayan bağlanma önemli ölçüde azalır. Gibi beyin omurilik sıvısı, eklem sıvısı, vb 6 gibi sınırlayıcı örnekleri ile çalışırken daha küçük örnek hacmi önemlidir. Tahlil multiplekslemesi daha tek bir örnekten çok sayıda sonuç sağlayarak, örnek hacmi gereksinimlerini azaltır. Luminex tarafından son gelişmeler şunlardır: Yeni MAGPIX sistemi, bir küçük, daha ucuz, kolay kullanımlı analizörü; Düşük Konsantrasyon Manyetik MagPlex Mikroküreler pahalı filtre plakaları olan ihtiyacı ortadan kaldırmak ve daha iyi analiz gelişimi için uygun bir çalışma konsantrasyonu gelir vedüşük hacimli uygulamalar ve xMAP Antikor Kaplin (AbC) Kit, bir protokol, reaktifler ve ilgi yakalama antikor boncuk bağlanması için gerekli sarf malzemeleri içerir. (Kit içeriğini ayrıntılı bir listesi için malzemeler bölümüne bakınız.) Bu deneyde, biz xMAP platformuna TNF-alfa sitokin için bir ön optimize ELISA testi dönüştürmek ve iki yöntem 7-11 performansını karşılaştırmak. TNF-alfa otoimmün hastalığı olan hastalarda inflamatuar yanıtların ölçümünde kullanılan bir biyolojik belirteç olduğunu. Biz dört farklı mikroküre setleri veya bölgelere dört aday yakalama antikorlar kaplin ile başlar. Birlikte karıştırıldığında, bu dört takım iyi antikor çifti, tasarruf reaktifler, örnek ve zamanı belirlemek için dört ayrı algılama antikorlar ile dört adayların aynı anda test için izin verir. İki xMAP testlerin ardından iki en iyi antikor çiftleri ile inşa ve performans edilirsinyal gücü, dinamik aralık ve duyarlılık konusunda özgün ELISA testi kıyasla.

Watch this Scientific Journal Video about Conversion of a Capture ELISA to a Luminex xMAP Assay using a Multiplex Antibody Screening Method at JoVE.com

Conversion of a Capture ELISA to a Luminex xMAP Assay using a Multiplex Antibody Screening Method

Bir ELISA kolayca Luminex xMAP assay dönüştürülebilir ve, çoğullama, çeşitli antikorların avantajları ile tahlil maliyet düşürürken, artan duyarlılık ve dinamik aralığı ile sonuçlanan, optimum bir antikor çifti tanımlamak için eşzamanlı taranabilir.

Bir Multiplex Antikor Tarama Yöntemi kullanılarak bir Luminex xMAP Tahlil için bir Capture ELISA Dönüşüm

The enzyme-linked immunosorbent assay (ELISA) has long been the primary tool for detection of analytes of interest in biological samples for both life ...

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JoVE Journal

Biology

43.4K Görüntüleme.  Luminex Corporation. Bir ELISA kolayca Luminex xMAP assay dönüştürülebilir ve, çoğullama, çeşitli antikorların avantajları ile tahlil maliyet düşürürken, artan duyarlılık ve dinamik aralığı ile sonuçlanan, optimum bir antikor çifti tanımlamak için eşzamanlı taranabilir.

Video: Conversion of a Capture ELISA to a Luminex xMAP Assay using a Multiplex Antibody Screening Method

Laser Capture Microdissection of Mammalian Tissue

Laser capture microscopy, also known as laser microdissection (LMD), enables the user to isolate small numbers of cells or tissues from frozen or formalin-fixed, paraffin-embedded tissue sections. LMD techniques rely on a thermo labile membrane placed either on top of, or underneath, the tissue section. In one method, focused laser energy is used to melt the membrane onto the underlying cells, which can then be lifted out of the tissue section. In the other, the laser energy vaporizes the foil along a path "drawn" on the tissue, allowing the selected cells to fall into a collection device. Each technique allows the selection of cells with a minimum resolution of several microns. DNA, RNA, protein, and lipid samples may be isolated and analyzed from micro-dissected samples. In this video, we demonstrate the use of the Leica AS-LMD laser microdissection instrument in seven segments, including an introduction to the principles of LMD, initializing the instrument for use, general considerations for sample preparation, mounting the specimen and setting up capture tubes, aligning the microscope, adjusting the capture controls, and capturing tissue specimens. Laser-capture micro-dissection enables the investigator to isolate samples of pure cell populations as small as a few cell-equivalents. This allows the analysis of cells of interest that are free of neighboring contaminants, which may confound experimental results.

Memeli Doku Lazer Yakalama Mikrodisseksiyon

Laser capture microscopy, also known as laser microdissection (LMD), enables the user to isolate small numbers of cells or tissues from frozen or ...

Biyoloji

Cell Capture Using a Microfluidic Device

Hücre Yakalama mikroakışkan Cihaz Kullanımı

Method for Whole Mount Antibody Staining in Chick

The chick embryo is a valuable tool in the study of early embryonic development. Its transparency, accessibility and ease of manipulation, make it an ideal tool for studying antibody expression in developing brain, neural tube and somite. This video demonstrates the different steps in whole-mount antibody staining using HRP conjugated secondary antibodies; First, the embryo is dissected from the egg and fixed in paraformaldehyde. Second, endogenous peroxidase is inactivated; The embryo is then exposed to primary antibody. After several washes, the embryo is incubated with secondary antibody conjugated to HRP. Peroxidase activity is revealed using reaction with diaminobenzidine substrate. Finally, the embryo is fixed and processed for photography and sectioning. The advantage of this method over the use of fluorescent antibodies is that embryos can be processed for wax sectioning, thus enabling the study of antigen sites in cross section. This method was originally introduced by Jane Dodd and Tom Jessell 1.

This video demonstrates whole mount immunohistochemistry, a method by which the spatial and temporal expression pattern of an antigen can be visualized in young chick embryos. This method was originally introduced by Jane Dodd and Tom Jessell.

Chick Tüm Dağı Antikor Boyama Yöntemi

The chick embryo is a valuable tool in the study of early embryonic development. Its transparency, accessibility and ease of manipulation, make it an ...

RNAi Screening to Identify Postembryonic Phenotypes in C. elegans

C. elegans has proven to be a valuable model system for the discovery and functional characterization of many genes and gene pathways1. More sophisticated tools and resources for studies in this system are facilitating continued discovery of genes with more subtle phenotypes or roles. 
Here we present a generalized protocol we adapted for identifying C. elegans genes with postembryonic phenotypes of interest using RNAi2. This procedure is easily modified to assay the phenotype of choice, whether by light or fluorescence optics on a dissecting or compound microscope. This screening protocol capitalizes on the physical assets of the organism and molecular tools the C. elegans research community has produced. As an example, we demonstrate the use of an integrated transgene that expresses a fluorescent product in an RNAi screen to identify genes required for the normal localization of this product in late stage larvae and adults. First, we used a commercially available genomic RNAi library with full-length cDNA inserts. This library facilitates the rapid identification of multiple candidates by RNAi reduction of the candidate gene product. Second, we generated an integrated transgene that expresses our fluorecently tagged protein of interest in an RNAi-sensitive background. Third, by exposing hatched animals to RNAi, this screen permits identification of gene products that have a vital embryonic role that would otherwise mask a post-embryonic role in regulating the protein of interest. Lastly, this screen uses a compound microscope equipped for single cell resolution.

RNAi Screening to Identify Postembryonic Phenotypes in C. elegans

We describe a sensitized method to identify postembryonic regulators of protein expression and localization in C. elegans using an RNAi-based genomic screen and an integrated transgene that expresses a functional, fluorescently tagged protein.

Içinde Postembryonic Fenotiplerin Belirleme RNAi Tarama C. elegans</em

C. elegans has proven to be a valuable model system for the discovery and functional characterization of many genes and gene pathways1. More sophisticated ...

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.

GIRK Kanal Modülatörler belirlenmesi için Floresan Tarama Testi

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

A Liquid Phase Affinity Capture Assay Using Magnetic Beads to Study Protein-Protein Interaction: The Poliovirus-Nanobody Example

In this article, a simple, quantitative, liquid phase affinity capture assay is presented. Provided that one protein can be tagged and another protein labeled, this method can be implemented for the investigation of protein-protein interactions. It is based on one hand on the recognition of the tagged protein by cobalt coated magnetic beads and on the other hand on the interaction between the tagged protein and a second specific protein that is labeled. First, the labeled and tagged proteins are mixed and incubated at room temperature. The magnetic beads, that recognize the tag, are added and the bound fraction of labeled protein is separated from the unbound fraction using magnets. The amount of labeled protein that is captured can be determined in an indirect way by measuring the signal of the labeled protein remained in the unbound fraction. The described liquid phase affinity assay is extremely useful when conformational conversion sensitive proteins are assayed. The development and application of the assay is demonstrated for the interaction between poliovirus and poliovirus recognizing nanobodies1. Since poliovirus is sensitive to conformational conversion2 when attached to a solid surface (unpublished results), the use of ELISA is limited and a liquid phase based system should therefore be preferred. An example of a liquid phase based system often used in polioresearch3,4 is the micro protein A-immunoprecipitation test5. Even though this test has proven its applicability, it requires an Fc-structure, which is absent in the nanobodies6,7. However, as another opportunity, these interesting and stable single-domain antibodies8 can be easily engineered with different tags. The widely used (His)6-tag shows affinity for bivalent ions such as nickel or cobalt, which can on their turn be easily coated on magnetic beads. We therefore developed this simple quantitative affinity capture assay based on cobalt coated magnetic beads. Poliovirus was labeled with 35S to enable unhindered interaction with the nanobodies and to make a quantitative detection feasible. The method is easy to perform and can be established with a low cost, which is further supported by the possibility of effectively regenerating the magnetic beads.

In this article, a simple, quantitative, liquid phase affinity capture assay is presented. It is a reliable technique based on the interaction between magnetic beads and tagged proteins (e.g. nanobodies) on one hand and the affinity between the tagged protein and a second, labeled protein (e.g. poliovirus) on the other.

Protein-Protein Etkileşimi Okumak Manyetik Boncuk Kullanarak Bir Sıvı Faz Affinity Yakalama Testi: Poliovirüs-Nanobody Örnek

In this article, a simple, quantitative, liquid phase affinity capture assay is presented. Provided that one protein can be tagged and another protein ...

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.

Bir ev yapımı Çift kızdırma Lusıferaz Testi kullanarak yüksek verim Fonksiyonel Taraması

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

A Method for Selecting Structure-switching Aptamers Applied to a Colorimetric Gold Nanoparticle Assay

Small molecules provide rich targets for biosensing applications due to their physiological implications as biomarkers of various aspects of human health and performance. Nucleic acid aptamers have been increasingly applied as recognition elements on biosensor platforms, but selecting aptamers toward small molecule targets requires special design considerations. This work describes modification and critical steps of a method designed to select structure-switching aptamers to small molecule targets. Binding sequences from a DNA library hybridized to complementary DNA capture probes on magnetic beads are separated from nonbinders via a target-induced change in conformation. This method is advantageous because sequences binding the support matrix (beads) will not be further amplified, and it does not require immobilization of the target molecule. However, the melting temperature of the capture probe and library is kept at or slightly above RT, such that sequences that dehybridize based on thermodynamics will also be present in the supernatant solution. This effectively limits the partitioning efficiency (ability to separate target binding sequences from nonbinders), and therefore many selection rounds will be required to remove background sequences. The reported method differs from previous structure-switching aptamer selections due to implementation of negative selection steps, simplified enrichment monitoring, and extension of the length of the capture probe following selection enrichment to provide enhanced stringency. The selected structure-switching aptamers are advantageous in a gold nanoparticle assay platform that reports the presence of a target molecule by the conformational change of the aptamer. The gold nanoparticle assay was applied because it provides a simple, rapid colorimetric readout that is beneficial in a clinical or deployed environment. Design and optimization considerations are presented for the assay as proof-of-principle work in buffer to provide a foundation for further extension of the work toward small molecule biosensing in physiological fluids.

A protocol is provided to select structure-switching aptamers for small molecule targets based on a tunable stringency magnetic bead selection method. Aptamers selected with structure-switching properties are beneficial for assays that require a conformational change to signal the presence of a target, such as the described gold nanoparticle assay.

Bir Kolorimetrik Altın Nanopartikül Testi Uygulanan Yapı-anahtarlama aptamers seçilmesi için bir yöntem

Small molecules provide rich targets for biosensing applications due to their physiological implications as biomarkers of various aspects of human health ...

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.

Yüksek Verimli Tarama kullanma Kinaz-substrat Çiftlerinin Kimlik


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

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).

Çok enzim Yüksek verim Genetik Enzim Eleme Sisteminin Kullanılması Eleme

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