JPH10503841A - 生体試料から成るミクロ配列を作成するための方法および装置 - Google Patents
生体試料から成るミクロ配列を作成するための方法および装置Info
- Publication number
- JPH10503841A JPH10503841A JP8502498A JP50249896A JPH10503841A JP H10503841 A JPH10503841 A JP H10503841A JP 8502498 A JP8502498 A JP 8502498A JP 50249896 A JP50249896 A JP 50249896A JP H10503841 A JPH10503841 A JP H10503841A
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.支持体上に被検体アッセイ領域から成るミクロ配列を形成する方法であっ て、ミクロ配列の各領域は既知量の選択された被検体特異試薬を有する配列を形 成する方法であって、 (a)選択された被検体特異試薬を含む溶液を(i)違いに離れて同一方向に広 がる細長い部材によって形成され、(ii)一定量の試薬溶液を保持することができ 、(iii)前記毛管流路中の水溶液がメニスカスを形成する先端領域を有する、細 長い毛管流路を有する試薬分配装置に充填するステップと、 (b)前記分配装置の先端を表面上の規定位置で支持体に対して軽く打ち付け 、毛管流路中のメニスカスを壊すように衝撃を与え、選択された量の溶液を表面 上に付着させるステップと、、 (c)ステップ(a)、(b)を前記配列が形成されるまで繰り返すステップ と を備えるミクロ配列形成方法。 2.前記打ち付けは、0.01nlないし100nlの範囲で選択された容量を付着させ るために効果的な衝撃を与えて行うことを特徴とする請求の範囲第1項記載のミ クロ配列形成方法。 3.前記流路は、一対の離れたテーパー要素によって形成されることを特徴と する請求の範囲第1項記載のミクロ配列形成方法。 4.上記のような複数の配列を形成するために、ステップ(b)を、ステップ (c)を進行する各反復サイクル時に、複数の支持体各々の上に選択された位置 で行うことを特徴とする請求の範囲第1項記載のミクロ配列形成方法。 5.ステップ(a)および(b)を少なくとも一回実施した後に、試薬分配装 置に新たな試薬溶液を、(i)試薬分配装置の毛管流路を洗浄溶液に浸すステップ と(ii)毛管流路に流れ込んだ洗浄溶液を除去するステップと、(iii)毛管流路に 新たな試薬溶液を浸すステップと、によって再充填するステップをさらに含むこ とを特徴とする請求の範囲第1項記載のミクロ配列形成方法。 6.複数の支持体上に被検体アッセイ領域から成るミクロ配列を形成する自動 装置であって、ミクロ配列の各領域は既知量の選択された被検体特異試薬を有す る自動装置であって、 (a)所定の位置に複数の平面支持体を保持するホルダーと、 (b)(i)互いに離れて同一方向に広がる細長い部材によって形成され、(ii) 一定量の試薬溶液を保持することができ、(iii)流路の水溶液がメニスカスを形 成する先端領域を有する、開口毛管流路を有する試薬分配装置と、 (c)分配装置を前記ホルダーの支持体に対して選択された配列位置に位置決 めする位置決め手段と、 (d)分配装置を支持体に対して規定の配列位置に位置決めしたときに、分配 装置を選択された衝撃で支持体に打ち付ける位置まで移動し、毛管流路の液体に よって生じるメニスカスを壊す衝撃を与え、選択された量の溶液を表面に付着さ せる付着手段と、 (e)前記位置決め手段と前記付着手段とを制御するための制御手段と、 を備える自動装置。 7.前記付着手段は、前記分配装置を支持体に対して効果的に移動させ、効果 的な衝撃を与えて、0.01ないし100nlの範囲で選択された量を付着させることを 特徴とする請求の範囲第6項記載の自動装置。 8.前記流路は、一対の互いに距離をあけたテーパー要素によって形成される ことを特徴とする請求の範囲第6項記載の自動装置。 9.前記制御手段は、(i)分配装置を充填位置に配置し、(ii)分配装置の毛管 流路を選択された試薬に充填位置で浸して、分配装置に試薬を充填し、(iii)試 薬を前記ホルダー上の各支持体上の規定の配列位置で分配するように動作するこ とを特徴とする請求の範囲第6項記載の自動装置。 10.前記制御装置は、分配サイクルの最後に、(i)分配装置を洗浄位置に配置 し、(ii)毛管流路を洗浄液に移動させてこれに浸し、分配装置に洗浄液を充填し 、(iii)分配装置に新鮮な選択された液を充填する前に、洗浄液を除去すること によって、分配装置を洗浄するようさらに動作することを特徴とする請求の範囲 第6項記載の自動装置。 11.前記分配装置は、異なる被検体アッセイ試薬を選択された互いに離れた位 置に配分するためのアームに備えられる複数の装置の1つであることを特徴とす る請求の範囲第6項記載の自動装置。 12.1cm2あたり少なくとも103個の異なるポリヌクレオチドまたはポリヌクレ オチド生体重合体から成るミクロ配列を含む表面を有し、各異なる生体重合体試 料は、(i)前記ミクロ配列の個別の規定の位置に付着され、(ii)少なくともサブ ユニット50個分の長さがあり、(iii)約0.1フェトモルから100ナノモルまでの規 定量で存在することを特徴とする基板。 13.前記表面は、ポリリシンで被覆されたスライドガラスであり、前記生体重 合体はポリヌクレオチドであることを特徴とする請求の範囲第12項記載の基板 。 14.前記基板は、非透水性の裏地と、透水性で裏地に形成されたフィルムと、 フィルムで形成された格子とを有し、前記格子は(i)前記裏地から前記フィルム の表面の上の高くした位置まで延在し交差する非透水性格子要素から成り、(ii) フィルムを複数の非透水性セルにしきられ、各セルは上記のような生体重合体配 列を収容することを特徴とする請求の範囲第12項記載の基板。 15.試料を収容するセルから成る表面配列を有する基板であって、 非透水性裏地と、 裏地に形成された透水性フィルムと、 前記フィルム上に形成された格子とを有し、 前記裏地から前記フィルムの表面上の高い位置まで延在し交差する非透水性格 子要素から成る前記格子を備える基板。 16.ミクロ配列のセルは、生体重合体の配列を含むことを特徴とする請求の範 囲第15項記載の基板。 17.標識生体重合体が複数の異なるポリヌクレオチドの1つ以上に結合してい ることを検出するために使用する基板であって、 非多孔性のガラス基板と、 前記基板上のカチオンポリマーから成る被覆と、 前記被覆に対して異なるポリヌクレオチドから成る配列であり、各生体重合体 は生体重合体から成る表面配列に個別に規定された位置に分配されることを特徴 とする基板。 18.第1の細胞タイプ中の複数の遺伝子各々の示差的な発現を、第2の細胞タ イプ中の同じ遺伝子の発現と比較して検出する方法であって、 蛍光標識cDNAを2つの細胞タイプから単離されたmRNAから生成し、第1の細胞 と第2の細胞から得たcDNAを第1および第2の蛍光リポーターで標識するステッ プと、 2つの細胞タイプから得た標識cDNAの混合物を、2つの細胞タイプに由来する複 数の既知の遺伝子を表現するポリヌクレオチドから成る配列に、cDNAを配列中の 相補的な配列であるポリヌクレオチドにハイブリダイゼーションさせる条件下で 添加するステップと、 (i)第1および第2の細胞タイプの1つに由来するcDNAに優先的にハイブリダ イズされる配列中のポリヌクレオチドが、第1または第2の異なる蛍光色をそれ ぞれ放出、(ii)第1および第2の細胞タイプに由来する実質的に等しい数のcDNA にハイブリダイズされる配列中のポリヌクレオチドが異なる組み合わせの蛍光色 をそれぞれ放出する、蛍光励起条件下で蛍光によって配列を試験するステップと を有し、2つの細胞タイプの既知の相対的発現を、各スポットで観察された蛍光 色の放出によって測定することができるようにした ことを備える検出方法。 19.ポリヌクレオチドの配列は、表面積が約1cm2未満に少なくとも102個の異 なるポリヌクレオチドまたはポリペプチド生体重合体から成る配列を含む表面を 有する基板上に形成され、各異なる生体重合体は、(i)前記配列に規定された個 別の位置に分配され、(ii)少なくともサブユニット50個分の長さを有し、(iii) 約0.1フェムトモルから100nmまでの規定量で存在することを特徴とする請求の範 囲第18項記載の検出方法。 20.前記表面は、ポリリシンで被覆されたスライドガラスであり、前記生体重 合体は前記ポリリシンに非共有的に結合されたポリヌクレオチドであることを特 徴とする請求の範囲第19項記載の検出方法。
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US26138894A | 1994-06-17 | 1994-06-17 | |
US08/477,809 US5807522A (en) | 1994-06-17 | 1995-06-07 | Methods for fabricating microarrays of biological samples |
US477,809 | 1995-06-07 | ||
US08/261,388 | 1995-06-07 | ||
US261,388 | 1995-06-07 | ||
US08/477,809 | 1995-06-07 |
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Also Published As
Publication number | Publication date |
---|---|
EP0804731B1 (en) | 1999-05-26 |
EP0913485A1 (en) | 1999-05-06 |
JP3272365B2 (ja) | 2002-04-08 |
DE69509925T2 (de) | 1999-12-09 |
CA2192095A1 (en) | 1995-12-28 |
CA2192005C (en) | 2005-10-25 |
EP0804731A4 (ja) | 1997-11-26 |
DK0804731T4 (da) | 2012-07-09 |
ES2134481T5 (es) | 2012-06-25 |
ATE180570T1 (de) | 1999-06-15 |
GR3030430T3 (en) | 1999-09-30 |
CA2192095C (en) | 1999-08-31 |
DK0804731T3 (da) | 1999-11-08 |
DE69509925T3 (de) | 2012-07-19 |
AU2862995A (en) | 1996-01-15 |
ES2134481T3 (es) | 1999-10-01 |
WO1995035505A1 (en) | 1995-12-28 |
EP0804731A1 (en) | 1997-11-05 |
DE69509925D1 (de) | 1999-07-01 |
AU709276B2 (en) | 1999-08-26 |
EP0804731B2 (en) | 2012-05-09 |
CA2192005A1 (en) | 1998-06-04 |
US6110426A (en) | 2000-08-29 |
JP2002243736A (ja) | 2002-08-28 |
US5807522A (en) | 1998-09-15 |
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