組換え抗体ネットワーク抗体選択および特性パイプラインとロボットの選択プラットフォームの資金調達購入のためのイノベーションのためのカナダの財団の開発に資金を提供するためのタンパク質捕獲試薬のプログラム-私たちは、NIHの共通基金を承認したいと思います。

<ol>
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著者らは、開示することは何もない。

体外抗体の選択で行う場合、選択成功の二つの主要な決定の際、選択するための、よく折り畳まれた抗原標的の1）分離と高機能の多様化抗体ライブラリの2）利用可能である。多くの場合、十分に折り畳まれた、全長タンパク質の十分な量の利用可能性を制限することができる。この制限を克服する1つのアプローチは、適切な親和性タグを細菌発現ベクターへの挿入のための生...

ポストゲノム時代の開始と、特徴づけるおよびタンパク質を調節する高品質の結合試薬の利用可能性は、新たな研究および治療の道を開くことが不可欠である。抗体は、基礎研究および診断ツールおよび潜在的な治療薬として、学術および産業研究者の両方に重要であり続ける。当然のことながら、カスタム抗体を生成するために、従来のハイブリドーマ技術に依存してそのほとんどが契約抗体開発企業の印象的な成長があった。それにもかかわらず、ファージディスプレイ抗体ライブラリーを用いたin vitroの選択は、従来の技術では限界が1、2に直面することができますユニークな利点と成功を提供することができる強力な代替技術になりつつある。 研究ツールとして、高品質の抗体についてのかなりの需要に照らして、再生可能な抗体を生成するための2つの主要な課題は、1）選択スループットおよび2）抗原avはあるailability。グループの数は、現在のスループットおよび抗体認識の速度を増加させることを目的とインビトロ選択パイプに記載されている。これらの説明は、詳細完全長ビーズベース6,8-またはプレートベース3,4抗原固定化スキームのいずれかを使用して、3,4、または構造的に関連するドメイン5,6,7を標的とするいずれかの際に選択することを含む実行可能な種々のアプローチを。さらに、遺伝子合成技術9の成長採用が合理的に費用効果と潜在的に精製された、完全長の抗原の十分な量を得ることが困難を緩和することができ、特に、単離されたドメインから、体系的抗原の生成を行った。タンデムに二つの技術を用いて、自己完結型のスケーラブルな抗原生成および抗体選択パイプラインは、発現される抗原ドメインの大きなセットのための抗体の並列単離を可能にし、茶のための試薬の開発を容易にするよう考案された構造的または機能的に関連するタンパク質の全体のクラスをracterizing。 この目的、表現可能な抗原ドメイン、遺伝子合成のインシリコ同定カップル統合されたパイプラインに向けて、抗原と拡張性のファージディスプレイされた抗体の選択のハイスループット細菌発現が開発されている。このパイプラインは、（ライセンスまたは材料移転契約を通じて、ますます利用できる抗体ライブラリを含む）は、ほとんどの生命科学研究室が利用できる唯一の​​基本的なインフラを必要としますが、工業規模での使用のためにも、自動化に適している。このプロトコルを使用して、親和性タグ化抗原ドメインの数百を生成することが可能であり、日常的には、これらの抗原の多くに非常に特異的な抗体断片を単離する。 ファージディスプレイ技術は、Fab、scFvは、自律のFvドメインであり、aを含む組換えアフィニティ試薬のさまざまな形式で実証互換性を示している小さ ​​な「代替フレームワーク」（設計されたアンキリンリピートタンパク質（ダルピン）、フィブロネクチン（FN）、リポカリンドメインと10以上）の成長配列。それは、これらの方法は、ライブラリーの他のタイプに適合させることができると推測されるが、議論は、Fab抗体フラグメントの単離この実施例では制限されている。この技術を用い、小さな低ナノモル親和性を有するFabを、全長タンパク質に結合し、そのような免疫蛍光法などのイムノアッセイにおいて機能的である多くはRNA結合タンパク質などが正常に選択された転写因子ドメイン、SH2ドメイン、を含むタンパク質ドメインをタグ付け、免疫沈降および免疫組織化学。重要なのは細菌の生産の提供を通じて、組換え結合クローンは、完全に再生可能であると表現構築から再生成することができ、したがって、厳密なクローンの検証の費用を正当化、一貫性、再現性と費用対効果を増加させた。 このPROTでocol及び添付ビデオは、固定化抗原ドメインを使用してファージディスプレイライブラリーからの抗体選択のための基本的な方法が実証されている。この特定の方法はまた、首尾よく使用されてきた13,14,2他のタグ11,12,13および選択フォーマットが、マイクロウェルプレートに受動的吸着により固定化されたGSTタグ付きタンパク質ドメインを使用する。特定と検証のために特別に濃縮されたクローン性抗体を単離することを目的とした選択パラメータの並列モニタリングと選択の設定や行動のための重要な考慮事項が詳述されている。

<table border="0" cellpadding="0" cellspacing="0" width="470">
	<tbody>
		<tr height="22">
			<td colspan="4" height="22" style="height:22px;width:471px;">MATERIALS</td>
		</tr>
		<tr height="43">
			<td colspan="2" height="43" style="height:43px;width:249px;">Name</td>
			<td style="width:135px;">Company</td>
			<td style="width:87px;">Catalog Number</td>
		</tr>
		<tr height="40">
			<td colspan="2" height="40" style="height:40px;width:249px;">New Brunswick Innova44 stackable incubator shaker</td>
			<td style="width:135px;">Eppendorf</td>
			<td style="width:87px;">M1282-0004</td>
		</tr>
		<tr height="40">
			<td colspan="2" height="40" style="height:40px;width:249px;">Liquidator 96 channel manual benchtop pipetting system</td>
			<td style="width:135px;">Anachem Ltd</td>
			<td style="width:87px;">LIQ-96-200</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">Microplate shaker</td>
			<td style="width:135px;">VWR</td>
			<td style="width:87px;">12620-926</td>
		</tr>
		<tr height="40">
			<td colspan="2" height="40" style="height:40px;width:249px;">ThermoScientific Sorvall ST-40 benchtop centrifuge</td>
			<td style="width:135px;">Thermo Product</td>
			<td style="width:87px;">75004525</td>
		</tr>
		<tr height="40">
			<td colspan="2" height="40" style="height:40px;width:249px;">ELx405 Select Deep Well Microplate Washer</td>
			<td style="width:135px;">Biotek</td>
			<td>ELX405USD</td>
		</tr>
		<tr height="41">
			<td colspan="2" height="41" style="height:41px;width:249px;">Custom High Throughput Automated Phage Selection Robot</td>
			<td style="width:135px;">S&#38;P Robotics</td>
			<td style="width:87px;"></td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">Plastic conical Falcon tube: 50 mL</td>
			<td style="width:135px;">VWR</td>
			<td style="width:87px;">21008-178</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">Plastic conical Falcon tube: 15 mL</td>
			<td style="width:135px;">VWR</td>
			<td style="width:87px;">89039-668</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">Axygen 1.7 mL microcentrifuge tubes</td>
			<td style="width:135px;">Corning</td>
			<td style="width:87px;">MCT-175-L-C</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">96-well/384-well Maxisorp plate</td>
			<td style="width:135px;">Sigma</td>
			<td style="width:87px;">M9410-1CS</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">Corning 96-well V-bottom deep-well block</td>
			<td style="width:135px;">Corning</td>
			<td style="width:87px;">3960</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">Axygen Mini-tube 96-well sterile microplate blue box</td>
			<td style="width:135px;">Corning</td>
			<td style="width:87px;">AXY-MTS-06-C-R-S</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">Breathable adhesive plate sealing film</td>
			<td style="width:135px;">VWR</td>
			<td style="width:87px;">60941-084</td>
		</tr>
		<tr height="22">
			<td colspan="4" height="22" style="height:22px;width:471px;">REAGENTS</td>
		</tr>
		<tr height="43">
			<td colspan="2" height="43" style="height:43px;width:249px;">Name</td>
			<td style="width:135px;">Company</td>
			<td style="width:87px;">Catalog Number</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">polyethylene glycol</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">PEG800.1</td>
		</tr>
		<tr height="18">
			<td colspan="2" height="18" style="height:18px;">yeast extract</td>
			<td>Bioshop</td>
			<td>YEX401.1</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">bio-tryptone</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">TRP402.1</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">N-Z amine</td>
			<td style="width:135px;">Sigma</td>
			<td style="width:87px;">C7290</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">glucose</td>
			<td style="width:135px;">Sigma</td>
			<td style="width:87px;">G8270-1KG</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">lactose</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">LAC234</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">glycerol</td>
			<td style="width:135px;">Bioshop</td>
			<td>GLY001.500</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">carbenicillin&#160;</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">CAR544.10</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">kanamycin</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">KAN201.25</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">tetracycline&#160;</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">TET701.25</td>
		</tr>
		<tr height="43">
			<td colspan="2" height="43" style="height:43px;width:249px;">Tween 20</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">TWN510.500</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">monobasic potassium phophate</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">PPM302.1</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">dibasic sodium phosphate</td>
			<td style="width:135px;">Anachemia</td>
			<td style="width:87px;">84486-440</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">sodium chloride</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">SOD001.10</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">potassium chloride</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">POC308.1</td>
		</tr>
		<tr height="20">
			<td colspan="2" height="20" style="height:20px;width:249px;">calcium chloride</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">CCL302.500</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">magnesium sulphate</td>
			<td style="width:135px;">EMD</td>
			<td style="width:87px;">MX0070-1</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">magnesium chloride</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">MAG510.500</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">NH4Cl</td>
			<td style="width:135px;">Amresco</td>
			<td style="width:87px;">0621-1KG</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">Na2SO4</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">SOS513.500</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">agar</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">AGR001.500</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">SybrSafe DNA gel stain</td>
			<td style="width:135px;">Invitrogen</td>
			<td style="width:87px;">S33102</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">phosphoric acid</td>
			<td style="width:135px;">Acros Organics</td>
			<td style="width:87px;">201140010</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">lysozyme</td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">LYS702.25</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">benzonase</td>
			<td style="width:135px;">Novagen</td>
			<td style="width:87px;">71205</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:139px;">Triton X-100</td>
			<td style="width:111px;"></td>
			<td style="width:135px;">Bioshop</td>
			<td style="width:87px;">TRX506.500</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="21" style="height:21px;width:249px;">protease inhibitor cocktail tablets</td>
			<td style="width:135px;">Roche</td>
			<td style="width:87px;">11 836 170 001</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">Ni-NTA resin&#160;</td>
			<td style="width:135px;">Qiagen</td>
			<td style="width:87px;">1018240</td>
		</tr>
		<tr height="42">
			<td colspan="2" height="42" style="height:43px;width:249px;">1000x helper phage (M13K07) stock (1013 phage per mL)</td>
			<td style="width:135px;">NEB</td>
			<td style="width:87px;">N0315S</td>
		</tr>
		<tr height="21">
			<td colspan="2" height="39" rowspan="2" style="height:40px;width:249px;">HRP conjugated M13-specific antibody (anti-M13-HRP).</td>
			<td rowspan="2" style="width:135px;">GE Healthcare</td>
			<td rowspan="2" style="width:87px;">27-9241-01</td>
		</tr>
		<tr height="18">
		</tr>
		<tr height="44">
			<td colspan="2" height="44" style="height:44px;width:249px;">TMB substrate: mix equal volumes of TMB and H2O2 peroxidase substrate&#160;</td>
			<td style="width:135px;">KPL</td>
			<td style="width:87px;">50-76-00</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">dNTPs</td>
			<td style="width:135px;">Biobasic</td>
			<td style="width:87px;">DD0056</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">Taq polymerase</td>
			<td style="width:135px;">Genscript</td>
			<td style="width:87px;">E00007</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">Exonuclease</td>
			<td style="width:135px;">GE Healthcare&#160;</td>
			<td style="width:87px;">EZ0073X-EZ</td>
		</tr>
		<tr height="22">
			<td colspan="2" height="22" style="height:22px;width:249px;">Shrimp alkaline phosphatase</td>
			<td style="width:135px;">GE Healthcare</td>
			<td style="width:87px;">E70092Z-EZ</td>
		</tr>
	</tbody>
</table>

scalable high throughput selection from  phage-displayed synthetic antibody libraries

両方の基礎および臨床研究用途のニーズを満たす抗体に対する要求が高く、劇的に、将来的に増加する。しかし、伝統的なモノクローナル技術は、このタスクまでだけではないことは明らかである。これは、プロテオームのアクセス可能なすべての要素を、高品質で再生可能な親和性試薬の需要を満たすために別の方法が開発された。そのために、ファージディスプレイされた合成抗体ライブラリーからの選択を行うためのハイスループット法は、多様な抗原を伴う用途のために考案されており、迅速なスループットと成功のために最適化された。ここで、プロトコルは、ビデオデモを手動96チャンネル液体ハンドラーまたは自動ロボットシステムのいずれかを使用してターゲットの数百に対して高い多様性ライブラリからのFabファージクローンの並列選択を示して詳細に説明する。このプロトコルを使用して、1人のユーザーが抗原の数百を生成することができ、並行して、それらに対する抗体を選択して、6〜8週間以内に結合する抗体を検証する。強調表示は、i）生存抗原フォーマット、ii）の事前選択抗原の特徴付け、iii）の特異的かつ高親和性クローンの選択に影響を与える重要なステップが、監視の選択の有効性および早期の抗体クローンの特徴付けのiv）の方法。このアプローチでは、我々は、シングルパス膜受容体を含む多くのターゲットクラスに分泌されるタンパク質ホルモン、及びマルチドメイン細胞内タンパク質を合成抗体断片（Fabを）取得している。これらの断片は、容易に完全長抗体に変換され、高い親和性および特異性を示すことが確認されている。さらに、それらは、ウエスタンブロッティング、ELISA、細胞の免疫蛍光、免疫沈降、および関連アッセイを含む標準的な免疫アッセイの様々な機能的であることが実証されている。この方法は、抗体の発見を加速し、最終的に目標Oの実現に近づく私たちをもたらすでしょうfのプロテオームの再生、高品質な抗体を生成する。

本明細書中に記載されるプロトコルは、並行して、コンビナトリアルファージディスプレイされたFabライブラリーからstructurally-と機能的に関連する抗原ドメインの両方の様々な抗体断片を単離するために使用されている。抗原の可用性に関連する問題は、抗体の選択23に適している発現可能な抗原ドメインのインシリコ同定によって、多くの場合、回避することができる。 （ ?...

Watch this Scientific Journal Video about Scalable High Throughput Selection From  Phage-displayed Synthetic Antibody Libraries at JoVE.com

Scalable High Throughput Selection From  Phage-displayed Synthetic Antibody Libraries

この方法は、同時に、抗原の何百に対するファージディスプレイコンビナトリアル合成抗体ライブラリーから、スケーラブルで高スループットの選択を行うための視覚的な伴奏して説明する。このパラレルアプローチを使用して、我々は、標準的な免疫アッセイにおいて機能的に多様な抗原に対する高い親和性および特異性を示す抗体断片を単離した。

ファージディスプレイされた合成抗体ライブラリーから、スケーラブルな高スループットの選択

The demand for antibodies that fulfill the needs of both basic and clinical research applications is high and will dramatically increase in the future. ...

scalable-high-throughput-selection-from-phage-displayed-synthetic

Research

JoVE Journal

Immunology and Infection

18.4K ビュー.  The Recombinant Antibody Network. この方法は、同時に、抗原の何百に対するファージディスプレイコンビナトリアル合成抗体ライブラリーから、スケーラブルで高スループットの選択を行うための視覚的な伴奏して説明する。このパラレルアプローチを使用して、我々は、標準的な免疫アッセイにおいて機能的に多様な抗原に対する高い親和性および特異性を示す抗体断片を単離した。 

ビデオ: Scalable High Throughput Selection From  Phage-displayed Synthetic Antibody Libraries

High-throughput Detection Method for Influenza Virus

Influenza virus is a respiratory pathogen that causes a high degree of morbidity and mortality every year in multiple parts of the world. Therefore, precise diagnosis of the infecting strain and rapid high-throughput screening of vast numbers of clinical samples is paramount to control the spread of pandemic infections. Current clinical diagnoses of influenza infections are based on serologic testing, polymerase chain reaction, direct specimen immunofluorescence and cell culture 1,2.
Here, we report the development of a novel diagnostic technique used to detect live influenza viruses. We used the mouse-adapted human A/PR/8/34 (PR8, H1N1) virus 3 to test the efficacy of this technique using MDCK cells 4. MDCK cells (104 or 5 x 103 per well) were cultured in 96- or 384-well plates, infected with PR8 and viral proteins were detected using anti-M2 followed by an IR dye-conjugated secondary antibody. M2 5 and hemagglutinin 1 are two major marker proteins used in many different diagnostic assays. Employing IR-dye-conjugated secondary antibodies minimized the autofluorescence associated with other fluorescent dyes. The use of anti-M2 antibody allowed us to use the antigen-specific fluorescence intensity as a direct metric of viral quantity. To enumerate the fluorescence intensity, we used the LI-COR Odyssey-based IR scanner. This system uses two channel laser-based IR detections to identify fluorophores and differentiate them from background noise. The first channel excites at 680 nm and emits at 700 nm to help quantify the background. The second channel detects fluorophores that excite at 780 nm and emit at 800 nm. Scanning of PR8-infected MDCK cells in the IR scanner indicated a viral titer-dependent bright fluorescence. A positive correlation of fluorescence intensity to virus titer starting from 102-105 PFU could be consistently observed. Minimal but detectable positivity consistently seen with 102-103 PFU PR8 viral titers demonstrated the high sensitivity of the near-IR dyes. The signal-to-noise ratio was determined by comparing the mock-infected or isotype antibody-treated MDCK cells.
Using the fluorescence intensities from 96- or 384-well plate formats, we constructed standard titration curves. In these calculations, the first variable is the viral titer while the second variable is the fluorescence intensity. Therefore, we used the exponential distribution to generate a curve-fit to determine the polynomial relationship between the viral titers and fluorescence intensities. Collectively, we conclude that IR dye-based protein detection system can help diagnose infecting viral strains and precisely enumerate the titer of the infecting pathogens.

This method describes the use of Infrared dye based imaging system for detection of H1N1 in bronchioalveolar lavage (BAL) fluid of infected mice at a high sensitivity. This methodology can be performed in a 96- or 384-well plate, requires &lt;10 &mu;l volume of test material and has the potential for concurrent screening of multiple pathogens.

インフルエンザウイルスのためのハイスループット検出方法

Influenza virus is a respiratory pathogen that causes a high degree of morbidity and mortality every year in multiple parts of the world. Therefore, ...

免疫・感染学

Quantitative High-throughput Single-cell Cytotoxicity Assay For T Cells

Cancer immunotherapy can harness the specificity of immune response to target and eliminate tumors. Adoptive cell therapy (ACT) based on the adoptive transfer of T cells genetically modified to express a chimeric antigen receptor (CAR) has shown considerable promise in clinical trials1-4. There are several advantages to using CAR+ T cells for the treatment of cancers including the ability to target non-MHC restricted antigens and to functionalize the T cells for optimal survival, homing and persistence within the host; and finally to induce apoptosis of CAR+ T cells in the event of host toxicity5.
Delineating the optimal functions of CAR+ T cells associated with clinical benefit is essential for designing the next generation of clinical trials. Recent advances in live animal imaging like multiphoton microscopy have revolutionized the study of immune cell function in vivo6,7. While these studies have advanced our understanding of T-cell functions in vivo, T-cell based ACT in clinical trials requires the need to link molecular and functional features of T-cell preparations pre-infusion with clinical efficacy post-infusion, by utilizing in vitro assays monitoring T-cell functions like, cytotoxicity and cytokine secretion. Standard flow-cytometry based assays have been developed that determine the overall functioning of populations of T cells at the single-cell level but these are not suitable for monitoring conjugate formation and lifetimes or the ability of the same cell to kill multiple targets8.
Microfabricated arrays designed in biocompatible polymers like polydimethylsiloxane (PDMS) are a particularly attractive method to spatially confine effectors and targets in small volumes9. In combination with automated time-lapse fluorescence microscopy, thousands of effector-target interactions can be monitored simultaneously by imaging individual wells of a nanowell array. We present here a high-throughput methodology for monitoring T-cell mediated cytotoxicity at the single-cell level that can be broadly applied to studying the cytolytic functionality of T cells.

We describe a single-cell high-throughput assay to measure cytotoxicity of T cells when incubated with tumor target cells. This method employs a dense, elastomeric array of sub-nanoliter wells (~100,000 wells/array) to spatially confine the T cells and target cells at defined ratios and is coupled to fluorescence microscopy to monitor effector-target conjugation and subsequent apoptosis.

T細胞の定量的なハイスループットシングルセル細胞毒性アッセイ

Cancer immunotherapy can harness the specificity of  immune response to target and eliminate tumors. Adoptive cell therapy (ACT)  based on the adoptive ...

High-throughput Screening for Broad-spectrum Chemical Inhibitors of RNA Viruses

RNA viruses are responsible for major human diseases such as flu, bronchitis, dengue, Hepatitis C or measles. They also represent an emerging threat because of increased worldwide exchanges and human populations penetrating more and more natural ecosystems. A good example of such an emerging situation is chikungunya virus epidemics of 2005-2006 in the Indian Ocean. Recent progresses in our understanding of cellular pathways controlling viral replication suggest that compounds targeting host cell functions, rather than the virus itself, could inhibit a large panel of RNA viruses. Some broad-spectrum antiviral compounds have been identified with host target-oriented assays. However, measuring the inhibition of viral replication in cell cultures using reduction of cytopathic effects as a readout still represents a paramount screening strategy. Such functional screens have been greatly improved by the development of recombinant viruses expressing reporter enzymes capable of bioluminescence such as luciferase. In the present report, we detail a high-throughput screening pipeline, which combines recombinant measles and chikungunya viruses with cellular viability assays, to identify compounds with a broad-spectrum antiviral profile.

In vitro assays to measure virus replication have been greatly improved by the development of recombinant RNA viruses expressing luciferase or other enzymes capable of bioluminescence. Here we detail a high-throughput screening pipeline that combines such recombinant strains of measles and chikungunya viruses to isolate broad-spectrum antivirals from chemical libraries.

RNAウイルスの広域スペクトルの化学抑制剤のためのハイスループットスクリーニング

RNA viruses are responsible for major human diseases such as flu, bronchitis, dengue, Hepatitis C or measles. They also represent an emerging threat ...

ScanLag: High-throughput Quantification of Colony Growth and Lag Time

Growth dynamics are fundamental characteristics of microorganisms. Quantifying growth precisely is an important goal in microbiology. Growth dynamics are affected both by the doubling time of the microorganism and by any delay in growth upon transfer from one condition to another, the lag. The ScanLag method enables the characterization of these two independent properties at the level of colonies originating each from a single cell, generating a two-dimensional distribution of the lag time and of the growth time. In ScanLag, measurement of the time it takes for colonies on conventional nutrient agar plates to be detected is automated on an array of commercial scanners controlled by an in house application. Petri dishes are placed on the scanners, and the application acquires images periodically. Automated analysis of colony growth is then done by an application that returns the appearance time and growth rate of each colony. Other parameters, such as the shape, texture and color of the colony, can be extracted for multidimensional mapping of sub-populations of cells. Finally, the method enables the retrieval of rare variants with specific growth phenotypes for further characterization. The technique could be applied in bacteriology for the identification of long lag that can cause persistence to antibiotics, as well as a general low cost technique for phenotypic screens.

ScanLag is a high-throughput method for measuring the delay in growth, namely lag time, as well as the growth rate of colonies for thousands of cells in parallel. Screening using ScanLag enables the discrimination between long lag-time and slow growth at the level of a single variant.

ScanLag：ハイスループットコロニーの成長の定量化とラグタイム

Growth dynamics are fundamental characteristics of microorganisms. Quantifying growth precisely is an important goal in microbiology. Growth dynamics are ...

High Yield Purification of Plasmodium falciparum Merozoites For Use in Opsonizing Antibody Assays

Plasmodium falciparum merozoite antigens are under development as potential malaria vaccines. One aspect of immunity against malaria is the removal of free merozoites from the blood by phagocytic cells. However assessing the functional efficacy of merozoite specific opsonizing antibodies is challenging due to the short half-life of merozoites and the variability of primary phagocytic cells. Described in detail herein is a method for generating viable merozoites using the E64 protease inhibitor, and an assay of merozoite opsonin-dependent phagocytosis using the pro-monocytic cell line THP-1. E64 prevents schizont rupture while allowing the development of merozoites which are released by filtration of treated schizonts. &#160;Ethidium bromide labelled merozoites are opsonized with human plasma samples and added to THP-1 cells. Phagocytosis is assessed by a standardized high throughput protocol. Viable merozoites are a valuable resource for assessing numerous aspects of P. falciparum biology, including assessment of immune function. Antibody levels measured by this assay are associated with clinical immunity to malaria in naturally exposed individuals. The assay may also be of use for assessing vaccine induced antibodies. &#160;

High Yield Purification of Plasmodium falciparum Merozoites For Use in Opsonizing Antibody Assays

Measuring antibody function is key to understanding immunity to Plasmodium falciparum malaria. This method describes the purification of viable merozoites, and measurement of opsonization-dependent phagocytosis by flow cytometry.

高収率の精製<em&gt;熱帯熱マラリア原虫</emオプソニン抗体アッセイにおける使用のための&gt;メロゾイト

Plasmodium falciparum merozoite antigens are under development as potential malaria vaccines. One aspect of immunity against malaria is the removal of ...

High-throughput Gene Tagging in Trypanosoma brucei

Improvements in mass spectrometry, sequencing and bioinformatics have generated large datasets of potentially interesting genes. Tagging these proteins can give insights into their function by determining their localization within the cell and enabling interaction partner identification. We recently published a fast and scalable method to generate Trypanosoma brucei cell lines that express a tagged protein from the endogenous locus. The method was based on a plasmid we generated that, when coupled with long primer PCR, can be used to modify a gene to encode a protein tagged at either terminus. This allows the tagging of dozens of trypanosome proteins in parallel, facilitating the large-scale validation of candidate genes of interest. This system can be used to tag proteins for localization (using a fluorescent protein, epitope tag or electron microscopy tag) or biochemistry (using tags for purification, such as the TAP (tandem affinity purification) tag). Here, we describe a protocol to perform the long primer PCR and the electroporation in 96-well plates, with the recovery and selection of transgenic trypanosomes occurring in 24-well plates. With this workflow, hundreds of proteins can be tagged in parallel; this is an order of magnitude improvement to our previous protocol and genome scale tagging is now possible.

High-throughput Gene Tagging in Trypanosoma brucei

Addition of a tag to a protein is a powerful way of gaining insight into its function. Here, we describe a protocol to endogenously tag hundreds of Trypanosoma brucei proteins in parallel such that genome scale tagging is achievable.

ハイスループット遺伝子タギングで<em&gt;トリパノソーマ</em

Improvements in mass spectrometry, sequencing and bioinformatics have generated large datasets of potentially interesting genes. Tagging these proteins ...

Construction of Synthetic Phage Displayed Fab Library with Tailored Diversity

Demand for monoclonal antibodies (mAbs) in basic research and medicine is increasing yearly. Hybridoma technology has been the dominant method for mAb development since its first report in 1975. As an alternative technology, phage display methods for mAb development are increasingly attractive since Humira, the first phage-derived antibody and one of the best-selling mAbs, was approved for clinical treatment of rheumatoid arthritis in 2002. As a non-animal based mAb development technology, phage display bypasses antigen immunogenicity, humanization, and animal maintenance that are required from traditional hybridoma technology based antibody development. In this protocol, we describe a method for construction of synthetic phage-displayed Fab libraries with diversities of 109-1010 obtainable with a single electroporation. This protocol consists of: 1) high-efficiency electro-competent cell preparation; 2) extraction of uracil-containing single-stranded DNA (dU-ssDNA); 3) Kunkel&#39;s method based oligonucleotide-directed mutagenesis; 4) electroporation and calculation of library size; 5) protein A/L-based enzyme-linked immunosorbent assay (ELISA) for folding and functional diversity evaluation; and 6) DNA sequence analysis of diversity.

This protocol describes a detailed procedure for the construction of a phage-displayed synthetic antibody library with tailored diversity. Synthetic antibodies have broad applications from basic research to disease diagnostics and therapeutics.

合成のバクテリオファージの建設は合わせた多様性と fab 抗体ライブラリーを表示

Demand for monoclonal antibodies (mAbs) in basic research and medicine is increasing yearly. Hybridoma technology has been the dominant method for mAb ...

A High-throughput, High-content, Liquid-based C. elegans Pathosystem

The number of new drugs identified by traditional, in vitro screens has waned, reducing the success of this approach in the search for new weapons to combat multiple drug resistance. This has led to the conclusion that researchers do not only need to find new drugs, but also need to develop new ways of finding them. Amongst the most promising candidate methods are whole-organism, in vivo assays that use high-throughput, phenotypic readouts and hosts that range from Caenorhabditis elegans to Danio rerio. These hosts have several powerful advantages, including dramatic reductions in false positive hits, as compounds that are toxic to the host and/or biounavailable are typically dropped in the initial screen, prior to costly follow up.
Here we show how our assay has been used to interrogate host variation in the well-documented C. elegans&#8212;Pseudomonas aeruginosa liquid killing pathosystem. We also demonstrate several extensions of this well-worked out technique. For example, we are able to carry out high-throughput genetic screens using RNAi in 24- or 96-well plate formats to query host factors in this host-pathogen interaction. Using this assay, whole genome screens can be completed in only a few months, which can dramatically simplify the task of identifying drug targets, potentially without the need for laborious biochemical purification approaches.
We also report here a variation of our method that substitutes the gram-positive bacterium Enterococcus faecalis for the gram-negative pathogen P. aeruginosa. Much as is the case for P. aeruginosa, killing by E. faecalis is time-dependent. Unlike previous C. elegans&#8212;E. faecalis assays, our assay for E. faecalis does not require preinfection, improving its safety profile and reducing the chances of contaminating liquid-handling equipment. The assay is highly robust, showing ~95% death rates 96 h post infection.

A High-throughput, High-content, Liquid-based C. elegans Pathosystem

Here we describe a protocol that is an adaptable, whole host, high-content screening tool that can be utilized to study host-pathogen interactions and be used for drug discovery.

高スループット、高コンテンツ、液体ベースのc. の elegans病態システム

The number of new drugs identified by traditional, in vitro screens has waned, reducing the success of this approach in the search for new weapons to ...

A High-throughput Shigella-specific Bactericidal Assay

Serum bactericidal assays (SBAs) measure the functional activity of antibodies and have been used for many decades. SBAs directly measure antibody killing activity by assessing the ability of antibodies in serum to bind to bacteria and activate complement. This complement activation results in the lysis and killing of the target bacteria. These assays are valuable because they go beyond quantifying antibody production to elucidate the biological functions that these antibodies have, allowing researchers to study the role that antibodies may play in preventing infection. SBAs have been used to study immune responses for many human pathogens, but there is no widely accepted methodology for Shigella at present. Historically, SBAs have been very labor-intensive, requiring many time-consuming steps to accurately quantify surviving bacteria. This protocol describes a simple, robust, and high-throughput assay that measures functional antibodies specific for Shigella in serum in vitro. The method described here offers many advantages over traditional SBAs, including the use of frozen bacterial stocks, 96 well assay plates, a micro-culture system, and automated colony-counting. All of these modifications make this assay less labor-intensive and more high-throughput. This protocol is simpler and faster to perform than traditional SBAs while still using simple technologies and readily available reagents. The protocol has been successfully applied in multiple independent laboratories and the assay is robust and reproducible. The assay can be used to assess immune responses in pre-clinical as well as clinical studies. Quantifying shigellacidal antibody titers both before and after antigen exposure (either by immunization or infection) allows for a broader understanding of how functional antibody responses are generated and their contribution to protective immunity. The development of this standardized, well-characterized assay may greatly facilitate Shigella vaccine design.

A High-throughput Shigella-specific Bactericidal Assay

Here we present a protocol to measure Shigellacidal activity of antibodies in serum. Serum is mixed with bacteria and exogenous complement, incubated, and the reaction mixture is plated on agar plates. Viable bacteria form colonies which are counted, using an automated colony enumerator, and used to determine the bactericidal titer.

高スループット赤痢菌-特定の殺菌試験

Serum bactericidal assays (SBAs) measure the functional activity of antibodies and have been used for many decades. SBAs directly measure antibody killing ...

Targeted Antibody Blocking by a Dual-Functional Conjugate of Antigenic Peptide and Fc-III Mimetics (DCAF)

Elimination of harmful antibodies from organisms is a valuable approach for the intervention of antibody-associated diseases, such as Dengue hemorrhagic fever and autoimmune diseases. Since thousands of antibodies with different epitopes are circulating in blood, no universal method, except for the dual-functional conjugate of antigenic peptide and Fc-III mimetics (DCAF), was reported to target specific harmful antibodies. The development of DCAF molecules makes significant contribution to the progress of targeted therapy, which were demonstrated to eliminate the antibody dependent enhancement (ADE) effect in a Dengue virus (DENV) infection model and to boost the acetylcholine receptor activity in a myasthenia gravis model. Here, we describe a protocol for the synthesis of a DCAF molecule (DCAF1), which can selectively block 4G2 antibody to attenuate ADE effect during Dengue virus infection, and illustrate the binding of DCAF1 to 4G2 antibody by an ELISA assay. In our method, DCAF1 is synthesized by the conjugation of a hydrazine derivative of a Fc-III peptide and a recombinant expressed long &#945;-helix with antigenic sequence through native chemical ligation (NCL). This protocol has been successfully applied to DCAF1 as well as other DCAF molecules for targeting their cognate antibodies.

Targeted Antibody Blocking by a Dual-Functional Conjugate of Antigenic Peptide and Fc-III Mimetics DCAF

Development of a dual-functional conjugate of antigenic peptide and Fc-III mimetics (DCAF) is novel for the elimination of harmful antibodies. Here, we describe a detailed protocol for the synthesis of DCAF1 molecule, which can selectively block 4G2 antibody to eliminate antibody dependent enhancement effect during Dengue virus infection.

抗原ペプチドとFc-III模倣体(DCAF)の二重機能コンジュゲートによる標的抗体遮断

Elimination of harmful antibodies from organisms is a valuable approach for the intervention of antibody-associated diseases, such as Dengue hemorrhagic ...