I. Hücreler Çözülme TN5 hücreler dondurulmuş flakon alın ve 37 ° C su banyosu içinde çözünme. 25cm 2 TC balon böcek Express orta 5ml (Invitrogen, katalog numarası 10486) ekleyin. Hızlı beş Glutamin olmadan geldiğini unutmayın; 100X glutamin kalem strep veya 1 lt medya tek başına Glutamine 10ml eklemek gerekir. TN5 hücrelerin içine ekleyin ve 30 dakika boyunca 27 ° C inkübatör inkübe. Daha sonra, balonun altına bağlanan hücreleri bozmadan nazikçe DMSO ile orta aspirat. Taze orta 5ml ekleyin. II. Yetiştirme ve Hücreler genişletilmesi Her gün hücrelerin izleyin. Balon yaklaşık% 70 konfluent olduğunda, her iki tarafta şişesi vurarak süspansiyon hücreleri getirmek ve Böcek ifade orta ve hücre kültürü 5ml 21 ml ekleyerek 175cm 2 balon hücreleri aktarmak. Her T175 şişesi, son bir birim olarak 25-30ml orta etrafında olmalıdır. Split konfluent balonuna (yaklaşık 1 milyon / ml kons.) Gerektiği şekilde 1 / 4 veya 1 / 5. Hücreleri büyümek izin vermeyin. Hücrelere bölünmüş olduğunu pasajların sayısını. Hücre lizis sonucu hücrelerin yaşlanma neden olabilir, çünkü geçit sayısı 30 üzerinde büyümeye etmeyin. 1 milyon / ml konsantrasyonda istenen birimde ulaştığınızda, hücreleri enfekte. Ben genellikle genellikle yetmiş 175cm 2 şişeler ve yaklaşık tutarı 2 ile 2,5 litre kadar büyüyebilir. 25 / 30ml balon ya da beş 1 litre Erlenmeyer şişeler ve yaklaşık. Her balona 400ml 500 ml Not: Ya T-175 fiş mühür şişesi veya Corning Erlenmeyer şişesinin hücreleri büyüyebilir. Erlenmeyer şişeler büyüyen hücreleri daha hızlı ve kolay. III. End Point Seyreltme Yöntemi Virüs Titering <ol><li> Hızlı beş SFM orta 200ul düz dipli 96 plaka Plaka 3000-5000 hücreleri de ortalama. Hücreler 27 ° C&#39;de en az 30 dakika dinlendiriniz. </li><li> Bakülovirüs stok seri seyreltme olun. Bir de ortalama 250ul kullanarak, 96 U alt plakası bir satır, 1 / 10 dilüsyon yapmak gerekir. Dilüsyonları Express Beş SFM ortamda yapılır. </li><li> Bir çok kanallı pipet kullanarak farklı dilüsyonları sabit tutar (genellikle 20 ul), hücrelere aktarın. </li><li> 27 ° C&#39;de 7 gün süreyle Kültür. Kenar satır buharlaşmasını önlemek için, parafilm ile plaka kenarları sarın. </li><li> 7 gün sonra, plaka kontrol ve virüs seyreltme% 50 enfeksiyon verir belirlemek bu virüs konsantrasyonu az yarım kuyu bulaşmış). Sonra pfu / ml (pfu-plak oluşturan birim) cinsinden ifade edilir titresi hesaplamak için bir formül kullanabilirsiniz. En bakülovirüs kılavuzları formül bulundu. </li></ol> IV. Hücrelerini enfekte Bu virüs Tam titresi bilmek çok önemlidir. Virüs gerekli miktarda ekleyin. Viral stok hazırlanması için hücreleri değil, daha Yüksek İçişleri Bakanlığı viral mutasyonlar üretimine neden olur (1pfu Beş hücre 1High) 1&#39;den Enfeksiyon Çokluk (İçişleri Bakanlığı) enfekte olmalıdır. Protein üretimi için, her zamanki miktarı MO1 5-10. Örnek: MCD1d bakülovirüs titresi = 1X108 pfu / ml Ekle İçişleri Bakanlığı = 1 (virüs yükseltmek için) = 20X10 ^ 6 hücre / şişeyi / 1x10 ^ 8 pfu / ml = 200 ul / şişesi İçişleri Bakanlığı = 5 - 10 (toplam protein üretimi için) 20x10 = 1ml için 2ml ^ 6 hücre / şişesi Enfeksiyon sonrası 4. günde, enfekte olmuş hücreleri bakmak. Onlar, yüzen, şişmiş ve şekillendirme sosis müstakil olmalıdır. V. kurtarma süpernatantlar Enfekte şişeler orta alın ve 250ml mavi kapaklı Falcon İplik şişe transfer. Otoklavlanabilir ve yeniden kullanılabilir. 200rpm, 20 dakika, 4 ° C de eşit şişe doldurun ve Sorvall GSA rotor hücreler santrifüj Süpernatantı toplayın ve daha ileri saflaştırma için devam edin. VI. Rekombinant mCD1d Of Arıtma <ol><li> Diyaliz ve Konsantrasyon 150mm Sodyum Fosfat tamponu (pH 7.4) </li><li> Ni-NTA Agaroz Kromatografi, 150mm Sodyum fosfat 200 mM Immidazole protein mCD1d + B2M Zehir </li><li> Tuzsuzlaştırma sütun Immidazole, kurtulmak için 20mm Tris HCl pH8 tampon kullanarak çalıştırın </li><li> Kalan kirleri ortadan kaldırmak için MonoQ sütun kullanarak Anyon Değişimi Kromatografisi çalıştırın. </li><li> YM 30 konsantratör (Millipore) kullanarak 1mg/ml için Konsantre </li><li> , Bira enzimatik biotynlation üretici protokolü (Avidite) göre mCD1d </li><li> Serbest biotin salin (PBS), pH7.4 tamponlanmış fosfat kullanarak S200 sütunu (boyut dışlama Chromatograpy) tarafından elimine edilir. Biotynlated protein 2 ila 3 MGS ortalama 2 litre süpernatant elde edilebilir </li><li> A-Galcer CD1d tetramer üretimi. </li></ol> A-Galcer çözünür biotynlated CD1d-b2 CD1d molekül yüklemek içinm PBS içinde% 0.5 Tween -20,% O.9 Sodyum Klorür çözünmüş bir Galcer üç kat molar fazlalığı, oda sıcaklığında bir gece inkübe edilir. Konjuge streptavidin ve oda sıcaklığında 4 saat için kuluçka Tetramers bir Galcer yüklü CD1d monomerlerin PE, 4 kat molar fazlası ile karıştırılarak oluşturulur. 48 ° C saklayınız

<ol>
	<li>Benlagha, K., Weiss, A., Beavis, A., Teyton, L., Bendelac, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=In+vivo+identification+of+glycolipipd+antigen-specific+T+cells+using+fluorecent+CD1d+tetramers.">In vivo identification of glycolipipd antigen-specific T cells using fluorecent CD1d tetramers.</a> J. Exp. Med. 191, 1895-1903 (2000).</li><li>Kinjo, Y., Wu, D., Kim, G., Xing, G. W., Poles, M. A., Ho, D. D., Tsuji, M., Kawahara, K., Wong, C. H., Kronenberg, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Recognition+of+bacterial+glycosphingolipids+by+natural+killer+T+cells.">Recognition of bacterial glycosphingolipids by natural killer T cells.</a> Nature. 434, 520-525 (2005).</li><li>Naidenko, O. V., Maher, J. K., Ernst, W. A., Sakai, T., Modlin, R. L., Kronenberg, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Binding+and+antigen+presentation+of+ceramide-containing+glycolipids+by+soluble+mouse+and+human+CD1d+molecules.">Binding and antigen presentation of ceramide-containing glycolipids by soluble mouse and human CD1d molecules.</a> J. Exp. Med. 190, 1069-1080 (1999).</li><li>Porcelli, S. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+CD1+family:+A+third+lineage+of+antigen-+presenting+molecules.">The CD1 family: A third lineage of antigen- presenting molecules.</a> Adv. Immunol. 59, 1-98 (1995).</li><li>Sidobre, S., Kronemberg, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=CD1+tetramers:+A+powerful+tool+for+the+analysis+of+glycolipid-reactive+T+cells.">CD1 tetramers: A powerful tool for the analysis of glycolipid-reactive T cells.</a> J. Immunol. 169, 1340-1348 (2002).</li></ol>

Bu yöntemde, başlatmak, büyümek, Böcek hücreleri enfekte ve bu hücreleri kullanarak bakülovirüs nasıl titresi nasıl gösterilir. Bu prosedürün en önemli yönlerinden hücrelerin korunması ve bakülovirüs tam titresi bilmek. CD1 tetramers yarattı, onlar glikolipid reaktif T hücrelerinin analizi için güçlü bir araç olarak kullanılabilir. Baculovirus sistemleri de MHC sınıf II tetramers bu nedenle bu işlemi çok daha geniş uygulanabilirliği içeren rekombinant proteinler üretmek için yaygın olarak kullanılmakta...

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		<div>
		<table border="1">
		<thead>
		<tr>
		<th>Material Name</th>
		<th>Type</th>
		<th>Company</th>
		<th>Catalogue Number</th>
		<th>Comment</th>
		</tr>
		</thead>
		<tbody>
		
<tr>
<td>Express Five SFM</td>
<td> Serum Free Medium</td>
<td>Invitrogen</td>
<td>10486025</td>
<td>&nbsp;</td>
<tr>
<td>High Five TM</td>
<td> Insect Cells</td>
<td>Invitrogen</td>
<td>B855-02</td>
<td>&nbsp;</td>
<tr>
<td>Glutamine Pen strep</td>
<td>Antibiotics</td>
<td>Invitrogen</td>
<td>10378-016</td>
<td>&nbsp;</td>
<tr>
<td>25cm2 TC Flask</td>
<td> Plastic</td>
<td>Fisher</td>
<td>10-126-28</td>
<td>&nbsp;</td>
<tr>
<td>175 cm2 TC Flask</td>
<td> Plug seal flask</td>
<td>Fisher</td>
<td>10-126-8</td>
<td>&nbsp;</td>
<tr>
<td>Erlenmeyer Flask</td>
<td> Cell Culture Flask</td>
<td>Fisher</td>
<td>07 200 672</td>
<td>&nbsp;</td>
<tr>
<td>YM 30 Concenterator</td>
<td>30,000 MWCO</td>
<td>Millipore</td>
<td>UFC 903096</td>
<td>&nbsp;</td>
<tr>
<td>FPLC equipment</td>
<td>&nbsp;</td>
<td>GE Healthcare</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>BrA Enzyme and Buffer</td>
<td> Biotinylation Kit</td>
<td>Avidity</td>
<td>BIRA500</td>
<td>&nbsp;</td>
<tr>
<td>Ni-NTA Agarose Column</td>
<td>His Tag Protein Purification Column</td>
<td>GE Healthcare</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>Desalting column</td>
<td> To get Rod of Salt from Protein</td>
<td>GE Healthcare</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>MonoQ Column</td>
<td>Anion Exchange Chromatgraphy</td>
<td>GE Healthcare</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>S200 Column</td>
<td> Size Exclusion Chromatography</td>
<td>GE Healthcare</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>alpha-Galcer</td>
<td> Glycolipid</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>PE- Streptavidin</td>
<td> For conjugating Protein</td>
<td>Molecular Probe</td>
<td> S-866</td>
<td>&nbsp;</td>		</tbody>
		</table>
		</div>

a method for production of recombinant mcd1d protein in insect cells.

CD1 proteinler antijen sunan moleküllerin üçüncü sınıf oluşturmaktadır. Onlar noncovalently beta2-mikroglobulin ile ilgili yaklaşık 50 kDa glikozile ağır zincir olarak ifade edilen hücre yüzey glikoprotein. Bu lipidler ziyade peptidler bağlanır. Kendi yapısı MHC sınıf I ve sınıf II antijen sunan moleküllerin CD1 proteinlerin benzerlik teyit rağmen, mCD1d oluk nispeten dar, derin ve son derece hidrofobik ve klasik için açıklanan birkaç sığ cepleri yerine iki bağlayıcı cepleri var MHC antijen sunan moleküller kodlanmış. Kendi amino asit dizilerinin dayanarak, böyle bir hydrobphobic oluk lipid antijenlerin bağlanması için ideal bir ortam sağlar. Doğal Öldürücü T (NKT) hücreleri, bağlı veya CD1d tarafından sunulan glikolipitler tanımak için kendi TCR kullanın. CD1 tarafından sunulan lipidler reaktif T hücrelerinin otoimmün ve bulaşıcı hastalıklara karşı koruma ve tümör rejeksiyon dahil edilmiştir. Böylece, CD1-reaktif NKT hücre yanıtı belirlemek, arındırmak ve izlemek için yeteneği büyük önem taşımaktadır. CD1d alfa Galactosyl seramid (a-Galcer) tetramers nesil NKT hücreleri biyoloji önemli bir anlayışa sahiptir. Diğer CD1 molekülleri inşa Tetramers de üretilen edilmiş ve bu yeni reaktifleri lipid tabanlı aşılara yanıt izlenmesinde potansiyel kullanımı ile büyük ölçüde ve otoimmün hastalıklar ve diğer tanı, lipid-reaktif T hücrelerinin fonksiyonları bilgi genişlettik tedaviler.

Watch this Scientific Journal Video about A Method For Production of Recombinant mCD1d Protein in Insect Cells. at JoVE.com

A Method For Production of Recombinant mCD1d Protein in Insect Cells.

Böcek hücreleri hazırlamak ve onları mCD1d tetramers üreten rekombinant mCD1d proteinand üretimi amacı bakülovirüs ile enfekte Bir Yöntem.

Rekombinant mCD1d Böcek Hücrelerde Protein Üretimi İçin Bir Yöntem.

CD1 proteins constitute a third class of antigen-presenting molecules. They are cell surface glycoproteins, expressed as approximately 50-kDa glycosylated ...

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Research

JoVE Journal

Biology

10.6K Görüntüleme.  La Jolla Institute for Allergy and Immunology. Böcek hücreleri hazırlamak ve onları mCD1d tetramers üreten rekombinant mCD1d proteinand üretimi amacı bakülovirüs ile enfekte Bir Yöntem.

Video: A Method For Production of Recombinant mCD1d Protein in Insect Cells.

A Protocol for Phage Display and Affinity Selection Using Recombinant Protein Baits

Using recombinant phage as a scaffold to present various protein portions encoded by a directionally cloned cDNA library to immobilized bait molecules is an efficient means to discover interactions. The technique has largely been used to discover protein-protein interactions but the bait molecule to be challenged need not be restricted to proteins. The protocol presented here has been optimized to allow a modest number of baits to be screened in replicates to maximize the identification of independent clones presenting the same protein. This permits greater confidence that interacting proteins identified are legitimate interactors of the bait molecule. Monitoring the phage titer after each affinity selection round provides information on how the affinity selection is progressing as well as on the efficacy of negative controls. One means of titering the phage, and how and what to prepare in advance to allow this process to progress as efficiently as possible, is presented. Attributes of amplicons retrieved following isolation of independent plaque are highlighted that can be used to ascertain how well the affinity selection has progressed. Trouble shooting techniques to minimize false positives or to bypass persistently recovered phage are explained. Means of reducing viral contamination flare up are discussed.

Phage display is a powerful technique to capture proteins or protein moieties that interact with an immobilized molecule of interest. Once a decision of the type of phage cDNA library to create and screen has been made, the protocol described here permits efficient affinity selection leading to identification of interactors.

Rekombinant Protein Yemler Kullanarak Phage Ekran ve Affinity seçimi için Protokol

Using  recombinant phage as a scaffold to present various protein portions encoded by  a directionally cloned cDNA library to immobilized bait molecules ...

Biyoloji

Efficient Production and Purification of Recombinant Murine Kindlin-3 from Insect Cells for Biophysical Studies

Kindlins are essential coactivators, with talin, of the cell surface receptors&#160;integrins and also participate in integrin outside-in signalling, and the control of gene transcription in the cell nucleus. The kindlins are ~75 kDa multidomain proteins and bind to an NPxY motif and upstream T/S cluster of the integrin &#946;-subunit cytoplasmic tail. The hematopoietically-important kindlin isoform, kindlin-3, is critical for platelet aggregation during thrombus formation, leukocyte rolling in response to infection and inflammation and osteoclast podocyte formation in bone resorption. Kindlin-3&#39;s role in these processes has resulted in extensive cellular and physiological studies. However, there is a need for an efficient method of acquiring high quality milligram quantities of the protein for further studies. We have developed a protocol, here described, for the efficient expression and purification of recombinant murine kindlin-3 by use of a baculovirus-driven expression system in Sf9 cells yielding sufficient amounts of high purity full-length protein to allow its biophysical characterization. The same approach could be taken in the study of the other mammalian kindlin isoforms.

Kindlins are fundamental to cell adhesion through integrins but studies of them have been hampered by the difficulty encountered in expressing them recombinantly in bacterial hosts. We describe here methods for their efficient production in baculovirus-infected insect cells.

Verimli Üretimi ve Saflaştırılması Rekombinant murin kindlin-3 Biophysical Çalışmaları Böcek hücrelerinden

Kindlins are essential coactivators, with talin, of the cell surface receptors&#160;integrins and also participate in integrin outside-in signalling, and ...

Investigating Protein-protein Interactions in Live Cells Using Bioluminescence Resonance Energy Transfer

Assays based on Bioluminescence Resonance Energy Transfer (BRET) provide a sensitive and reliable means to monitor protein-protein interactions in live cells. BRET is the non-radiative transfer of energy from a 'donor' luciferase enzyme to an 'acceptor' fluorescent protein. In the most common configuration of this assay, the donor is Renilla reniformis luciferase and the acceptor is Yellow Fluorescent Protein (YFP). Because the efficiency of energy transfer is strongly distance-dependent, observation of the BRET phenomenon requires that the donor and acceptor be in close proximity. To test for an interaction between two proteins of interest in cultured mammalian cells, one protein is expressed as a fusion with luciferase and the second as a fusion with YFP. An interaction between the two proteins of interest may bring the donor and acceptor sufficiently close for energy transfer to occur. Compared to other techniques for investigating protein-protein interactions, the BRET assay is sensitive, requires little hands-on time and few reagents, and is able to detect interactions which are weak, transient, or dependent on the biochemical environment found within a live cell. It is therefore an ideal approach for confirming putative interactions suggested by yeast two-hybrid or mass spectrometry proteomics studies, and in addition it is well-suited for mapping interacting regions, assessing the effect of post-translational modifications on protein-protein interactions, and evaluating the impact of mutations identified in patient DNA.

Interactions between proteins are fundamental to all cellular processes. Using Bioluminescence Resonance Energy Transfer, the interaction between a pair of proteins can be monitored in live cells and in real time. Furthermore, the effects of potentially pathogenic mutations can be assessed.

Biyoparlaklık Rezonans Enerji Transferi kullanma Canlı Hücrelerde Protein-protein etkileşimleri araştıran

Assays based on Bioluminescence Resonance Energy Transfer (BRET) provide a sensitive and reliable means to monitor protein-protein interactions in live ...

Recombinant Protein Expression for Structural Biology in HEK 293F Suspension Cells: A Novel and Accessible Approach

The expression and purification of large amounts of recombinant protein complexes is an essential requirement for structural biology studies. For over two decades, prokaryotic expression systems such as E. coli have dominated the scientific literature over costly and less efficient eukaryotic cell lines. Despite the clear advantage in terms of yields and costs of expressing recombinant proteins in bacteria, the absence of specific co-factors, chaperones and post-translational modifications may cause loss of function, mis-folding and can disrupt protein-protein interactions of certain eukaryotic multi-subunit complexes, surface receptors and secreted proteins. The use of mammalian cell expression systems can address these drawbacks since they provide a eukaryotic expression environment. However, low protein yields and high costs of such methods have until recently limited their use for structural biology. Here we describe a simple and accessible method for expressing and purifying milligram quantities of protein by performing transient transfections of suspension grown HEK (Human Embryonic Kidney) 293F cells.

The expression of recombinant proteins by mammalian systems is becoming an attractive method for producing protein complexes for structural biology. Here we present a simple yet highly efficient expression system using suspension grown mammalian cells to purify protein complexes for structural studies.

Bir Roman ve Erişilebilir Yaklaşım: Yapısal HEK 293F Askı Hücreleri Biyoloji Rekombinant Protein

The expression and purification of large amounts of recombinant protein complexes is an essential requirement for structural biology studies. For over two ...

Green Fluorescent Protein-based Expression Screening of Membrane Proteins in Escherichia coli

The production of recombinant membrane proteins for structural and functional studies remains technically challenging due to low levels of expression and the inherent instability of many membrane proteins once solubilized in detergents. A protocol is described that combines ligation independent cloning of membrane proteins as GFP fusions with expression in Escherichia coli detected by GFP fluorescence. This enables the construction and expression screening of multiple membrane protein/variants to identify candidates suitable for further investment of time and effort. The GFP reporter is used in a primary screen of expression by visualizing GFP fluorescence following SDS polyacrylamide gel electrophoresis (SDS-PAGE). Membrane proteins that show both a high expression level with minimum degradation as indicated by the absence of free GFP, are selected for a secondary screen. These constructs are scaled and a total membrane fraction prepared and solubilized in four different detergents. Following ultracentrifugation to remove detergent-insoluble material, lysates are analyzed by fluorescence detection size exclusion chromatography (FSEC). Monitoring the size exclusion profile by GFP fluorescence provides information about the mono-dispersity and integrity of the membrane proteins in different detergents. Protein: detergent combinations that elute with a symmetrical peak with little or no free GFP and minimum aggregation are candidates for subsequent purification. Using the above methodology, the heterologous expression in E. coli of SED (shape, elongation, division, and sporulation) proteins from 47 different species of bacteria was analyzed. These proteins typically have ten transmembrane domains and are essential for cell division. The results show that the production of the SEDs orthologues in E. coli was highly variable with respect to the expression levels and integrity of the GFP fusion proteins. The experiment identified a subset for further investigation.

Green Fluorescent Protein-based Expression Screening of Membrane Proteins in Escherichia coli

A streamlined approach to screening for the expression of recombinant membrane proteins in Escherichia coli based on fusion to green fluorescent protein is presented.

Membran proteinlerinin Yeşil floresan proteini temelli Ekspresyon elemesinde<em&gt; Escherichia coli</em

The production of recombinant membrane proteins for structural and functional studies remains technically challenging due to low levels of expression and ...

A Comparative Analysis of Recombinant Protein Expression in Different Biofactories: Bacteria, Insect Cells and Plant Systems

Plant-based systems are considered a valuable platform for the production of recombinant proteins as a result of their well-documented potential for the flexible, low-cost production of high-quality, bioactive products.
In this study, we compared the expression of a target human recombinant protein in traditional fermenter-based cell cultures (bacterial and insect) with plant-based expression systems, both transient and stable.
For each platform, we described the set-up, optimization and length of the production process, the final product quality and the yields and we evaluated provisional production costs, specific for the selected target recombinant protein.
Overall, our results indicate that bacteria are unsuitable for the production of the target protein due to its accumulation within insoluble inclusion bodies. On the other hand, plant-based systems are versatile platforms that allow the production of the selected protein at lower-costs than Baculovirus/insect cell system. In particular, stable transgenic lines displayed the highest-yield of the final product and transient expressing plants the fastest process development. However, not all recombinant proteins may benefit from plant-based systems but the best production platform should be determined empirically with a case-by-case approach, as described here.

In this study the expression of a target human recombinant protein in different production platforms was compared. We focused on traditional fermenter-based cultures and on plants, describing the set-up of each system and highlighting, on the basis of the reported results, the inherent limits and advantages for each platform.

Bakteriler, Böcek Hücreleri ve Bitki Sistemleri: Rekombinant Protein Farklı Biofactories İfade Karşılaştırmalı Analizi

Plant-based systems are considered a valuable platform for the production of recombinant proteins as a result of their well-documented potential for the ...

Nephrotoxin Microinjection in Zebrafish to Model Acute Kidney Injury

The kidneys are susceptible to harm from exposure to chemicals they filter from the bloodstream. This can lead to organ injury associated with a rapid decline in renal function and development of the clinical syndrome known as acute kidney injury (AKI). Pharmacological agents used to treat medical circumstances ranging from bacterial infection to cancer, when administered individually or in combination with other drugs, can initiate AKI. Zebrafish are a useful animal model to study the chemical effects on renal function in vivo, as they form an embryonic kidney comprised of nephron functional units that are conserved with higher vertebrates, including humans. Further, zebrafish can be utilized to perform genetic and chemical screens, which provide opportunities to elucidate the cellular and molecular facets of AKI and develop therapeutic strategies such as the identification of nephroprotective molecules. Here, we demonstrate how microinjection into the zebrafish embryo can be utilized as a paradigm for nephrotoxin studies.

Renal injuries incurred from nephrotoxins, which include drugs ranging from antibiotics to chemotherapeutics, can result in complex disorders whose pathogenesis remains incompletely understood. This protocol demonstrates how zebrafish can be used for disease modeling of these conditions, which can be applied to the identification of renoprotective measures.

Zebra balığı Nephrotoxin Mikroenjeksiyon Akut Böbrek Yaralanması Model

The kidneys are susceptible to harm from exposure to chemicals they filter from the bloodstream. This can lead to organ injury associated with a rapid ...

A Graphical User Interface for Software-assisted Tracking of Protein Concentration in Dynamic Cellular Protrusions

Filopodia are dynamic, finger-like cellular protrusions associated with migration and cell-cell communication. In order to better understand the complex signaling mechanisms underlying filopodial initiation, elongation and subsequent stabilization or retraction, it is crucial to determine the spatio-temporal protein activity in these dynamic structures. To analyze protein function in filopodia, we recently developed a semi-automated tracking algorithm that adapts to filopodial shape-changes, thus allowing parallel analysis of protrusion dynamics and relative protein concentration along the whole filopodial length. Here, we present a detailed step-by-step protocol for optimized cell handling, image acquisition and software analysis. We further provide instructions for the use of optional features during image analysis and data representation, as well as troubleshooting guidelines for all critical steps along the way. Finally, we also include a comparison of the described image analysis software with other programs available for filopodia quantification. Together, the presented protocol provides a framework for accurate analysis of protein dynamics in filopodial protrusions using image analysis software.

We present a software solution for semi-automated tracking of relative protein concentration along the length of dynamic cellular protrusions.

Dinamik Hücresel Protrüzyonlarda Protein Konsantrasyonunun Yazılım Destekli Takibi için Grafiksel Bir Kullanıcı Arayüzü

Filopodia are dynamic, finger-like cellular protrusions associated with migration and cell-cell communication. In order to better understand the complex ...

Transient Expression and Cellular Localization of Recombinant Proteins in Cultured Insect Cells

Heterologous protein expression systems are used for the production of recombinant proteins, the interpretation of cellular trafficking/localization, and the determination of the biochemical function of proteins at the sub-organismal level. Although baculovirus expression systems are increasingly used for protein production in numerous biotechnological, pharmaceutical, and industrial applications, nonlytic systems that do not involve viral infection have clear benefits but are often overlooked and underutilized. Here, we describe a method for generating nonlytic expression vectors and transient recombinant protein expression. This protocol allows for the efficient cellular localization of recombinant proteins and can be used to rapidly discern protein trafficking within the cell. We show the expression of four&#160;recombinant proteins in a commercially available insect cell line, including two aquaporin proteins from the insect Bemisia tabaci, as well as subcellular marker proteins specific for the cell plasma membrane and for intracellular lysosomes. All recombinant proteins were produced as chimeras with fluorescent protein markers at their carboxyl termini, which allows for the direct detection of the recombinant proteins. The double transfection of cells with plasmids harboring constructs for the genes of interest and a known subcellular marker allows for live cell imaging and improved validation of cellular protein localization.

Nonlytic insect cell expression systems are underutilized for production, cellular trafficking/localization, and recombinant protein functional analysis. Here, we describe methods to generate expression vectors and subsequent transient protein expression in commercially available lepidopteran cell lines. The co-localization of Bemisia tabaci aquaporins with subcellular fluorescent marker proteins is also presented.

Kültürlü Böcek Hücrelerinde Geçici İfade ve Rekombinant Proteinlerin Hücresel Yerelleştirme

Heterologous protein expression systems are used for the production of recombinant proteins, the interpretation of cellular trafficking/localization, and ...

E. coli'den Rekombinant Protein Dolu Veziküllerin Üretimi ve Görüntülenmesi

Optimized Production and Analysis of Recombinant Protein-Filled Vesicles from E. coli

This innovative system, using a short peptide tag, that exports multiple recombinant proteins in membrane bound vesicles from E. coli, provides an effective solution to a range of problems associated with bacterial recombinant protein expression. These recombinant vesicles compartmentalise proteins within a micro-environment that facilitates the production of otherwise challenging, toxic, insoluble, or disulfide-bond containing proteins from bacteria. Protein yield is increased considerably when compared to typical bacterial expression in the absence of the vesicle-nucleating peptide tag. The release of vesicle-packaged proteins supports isolation from the culture medium&#160;and permits long-term active protein storage. This technology gives rise to increased yields of vesicle-packaged, functional proteins for simplified downstream processing for a diverse range of applications from applied biotechnology to discovery science and medicine. In the present article and the associated video, a detailed protocol of the method is provided, which highlights key steps in the methodology to maximize recombinant protein-filled vesicle production.

Yazar Spotlight: Rekombinant Proteinlerin Üretimi 

The present protocol describes a detailed method for the bacterial production of recombinant proteins, including typically insoluble or disulfide-bond containing proteins, packaged inside extracellular membrane-bound vesicles. This has the potential to be applied to versatile areas of scientific research, including applied biotechnology and medicine.