JP7473398B2 - キャリブレータ、複合体、及びIgA凝集体を測定する方法 - Google Patents
キャリブレータ、複合体、及びIgA凝集体を測定する方法 Download PDFInfo
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- JP7473398B2 JP7473398B2 JP2020093435A JP2020093435A JP7473398B2 JP 7473398 B2 JP7473398 B2 JP 7473398B2 JP 2020093435 A JP2020093435 A JP 2020093435A JP 2020093435 A JP2020093435 A JP 2020093435A JP 7473398 B2 JP7473398 B2 JP 7473398B2
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Classifications
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- C07K16/42—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against immunoglobulins
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07K16/06—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies from serum
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/34—Genitourinary disorders
- G01N2800/347—Renal failures; Glomerular diseases; Tubulointerstitial diseases, e.g. nephritic syndrome, glomerulonephritis; Renovascular diseases, e.g. renal artery occlusion, nephropathy
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Description
1.測定用試薬の調製
(1.1) 試料希釈用緩衝液(第1試薬)
試料希釈用緩衝液として、1%BSA含有10 mM HEPES(pH7.5)を調製した。
WFAレクチン(ベクター・ラボラトリーズ社)を20 mM PBS(pH7.5)に添加し、WFA含有溶液(WFA濃度2.5 mg/mL)を得た。このWFA含有溶液に、ビオチン基を有する架橋剤である5-(N-スクシンイミジルオキシカルボニル)ペンチルD-ビオチンアミド(Biotin-AC5-Osu、株式会社同仁化学研究所)を、WFA/架橋剤(モル比)が1/100となるように添加した。得られた溶液を25℃で90分間インキュベーションして、WFAと架橋剤とを反応させた。得られた反応産物をHPLCにより精製して、ビオチン化二量体WFAを得た。HPLCには、分離カラムとしてゲルろ過カラム(TSKgel G3000SWXL、東ソー株式会社)を用い、溶出溶媒としてPBS(pH6.5)を用いた。ストレプトアビジン結合磁性粒子を含む懸濁液として、HISCL R2試薬(シスメックス株式会社)を用いた。ビオチン化二量体WFAとHISCL R2試薬とを、ビオチン化二量体WFAの濃度が20μg/mLとなるように混合して反応させた。得られた反応産物を100 mM MES緩衝液(pH6.5)で3回洗浄し、二量体WFAを固定した磁性粒子(以下、「WFA固定化粒子」ともいう)を得た。
抗IgA抗体として、抗ヒトIgA抗体(SouthernBiotech)を用いた。この抗IgA抗体とウシ小腸由来ALP(オリエンタル酵母株式会社)とを、マレイミド架橋剤を用いて結合させ、アフィニティクロマトグラフィーにより精製して、ALP標識抗IgA抗体を含む溶液を得た。
測定用緩衝液として、HISCL R4試薬(シスメックス株式会社)を用いた。基質溶液として、ALPの化学発光基質であるCDP-Star(商標)(アプライドバイオシステムズ社)を含むHISCL R5試薬(シスメックス株式会社)を用いた。
(2.1) ビオチン基を有するIgAの調製
IgA単量体として、ヒトIgA(Native Human IgA protein、Abcam社)を用いた。ヒトIgAを20 mM PBS(pH7.5)に添加してIgA溶液を得た。このIgA溶液に架橋剤Biotin-AC5-Osu(株式会社同仁化学研究所)を、IgA/架橋剤(モル比)が1/100となるように添加した。得られた溶液を25℃で90分間インキュベーションして、ビオチン化IgAを得た。
キャリアタンパク質として、M2BP(シスメックス社調製品)、MUC1(シスメックス社調製品)及びα2M(シグマアルドリッチ)を用いた。各キャリアタンパク質を20 mM PBS(pH7.5)に添加して、キャリアタンパク質の溶液を得た。この溶液に架橋剤Biotin-AC5-Osu(株式会社同仁化学研究所)を、キャリアタンパク質/架橋剤(モル比)が1/100となるように添加した。得られた溶液を25℃で90分間インキュベーションして、ビオチン化キャリアタンパク質を得た。
ビオチン化IgAを含む溶液と、ストレプトアビジン(Streptavidin SQ、ロシュ・ダイアグノスティックス株式会社)を含む溶液とを混合し、室温で1時間静置して、ビオチン化IgAとストレプトアビジンとの複合体(以下、「IgA-Bio-STA-Bio-IgA」とも呼ぶ)を得た。
各ビオチン化キャリアタンパク質の溶液と、ビオチン化IgAを含む溶液とを混合した。得られた混合液と、ストレプトアビジン(Streptavidin SQ、ロシュ・ダイアグノスティックス株式会社)を含む溶液とを混合し、室温で1時間静置して、ビオチン化IgAとビオチン化キャリアタンパク質とストレプトアビジンとの複合体(0.2 mg/mL)を得た。以下、M2BPを含む複合体を「M2BP-Bio-STA-Bio-IgA」とも呼び、MUC1を含む複合体を「MUC1-Bio-STA-Bio-IgA」とも呼び、α2Mを含む複合体を「A2M-Bio-STA-Bio-IgA」とも呼ぶ。
上記の第1試薬から第5試薬を用いて全自動免疫測定装置HISCL(商標)5000(シスメックス株式会社)により、キャリブレータとして、M2BP-Bio-STA-Bio-IgA、MUC1-Bio-STA-Bio-IgA及びA2M-Bio-STA-Bio-IgAのそれぞれを測定した。HISCL-5000による測定手順は、次のとおりであった。キャリブレータ(30μL)と第1試薬(100μL)とを混合した後、第2試薬(30μL)を添加した。得られた混合液中の磁性粒子を集磁して上清を除き、HISCL洗浄液(300μL)を加えて磁性粒子を洗浄した。上清を除き、磁性粒子に第3試薬(100μL)を添加して混合した。得られた混合液中の磁性粒子を集磁して上清を除き、HISCL洗浄液(300μL)を加えて磁性粒子を洗浄した。上清を除き、磁性粒子に第4試薬(50μL)及び第5試薬(100μL)を添加して、化学発光強度を測定した。対照として、ストレプトアビジン(STA)及び各ビオチン化キャリアタンパク質(M2BP-Bio、MUC1-Bio及びA2M-Bio)を同様に測定した。測定値(シグナルカウント)を表1に示す。
キャリブレータとして、M2BP-Bio-STA-Bio-IgA、MUC1-Bio-STA-Bio-IgA、A2M-Bio-STA-Bio-IgA及びIgA-Bio-STA-Bio-IgAを用いた。各キャリブレータを20 mM PBS(pH7.5)で5倍、25倍及び125倍に希釈したこと以外は、上記と同様にして測定した。測定値(シグナルカウント)を表2に示す。
11、21、31: 第1容器
12、23、34: 梱包箱
13、24、35: 添付文書
22、32: 第2容器
33: 第3容器
Claims (13)
- ビオチン基を有するIgAと、アビジン類と、レクチンと結合する糖鎖及びビオチン基を有するポリペプチドとの複合体を含む試薬である、試料中のIgA凝集体の濃度を取得するために用いられるキャリブレータ。
- 前記ポリペプチドが、M2BP、MUC1及びα2Mからなる群より選択される少なくとも1の糖タンパク質の全部又は一部を含む請求項1に記載のキャリブレータ。
- 試料中のIgA凝集体の濃度を取得するために用いられる、ビオチン基を有するIgAと、アビジン類と、レクチンと結合する糖鎖及びビオチン基を有するポリペプチドとの複合体。
- 前記ポリペプチドが、M2BP、MUC1及びα2Mからなる群より選択される少なくとも1の糖タンパク質の全部又は一部を含む請求項3に記載の複合体。
- レクチンを用いて試料中のIgA凝集体を測定する方法であって、
ビオチン基を有するIgAと、アビジン類と、レクチンと結合する糖鎖及びビオチン基を有するポリペプチドとの複合体を含む試薬であるキャリブレータを用いて、前記試料中のIgA凝集体の濃度を取得することを含む、前記方法。 - 前記ポリペプチドが、M2BP、MUC1及びα2Mからなる群より選択される少なくとも1の糖タンパク質の全部又は一部を含む請求項5に記載の方法。
- 前記キャリブレータが、前記複合体をそれぞれ含む複数の試薬を含む試薬セットであり、前記複数の試薬における前記複合体の濃度が互いに異なっている請求項5又は6に記載の方法。
- 前記試料と、前記レクチンと、標識物質を含み且つ前記IgA凝集体に特異的に結合する捕捉体とを用いて、前記IgA凝集体の測定値を取得する工程と、
前記キャリブレータと、前記レクチンと、前記捕捉体とを用いて、前記複合体の測定値を取得する工程と、
前記IgA凝集体の測定値及び前記複合体の測定値から、前記試料中のIgA凝集体の濃度を取得する工程と
を含む請求項5~7のいずれか1項に記載の方法。 - 前記IgA凝集体の濃度の取得工程において、前記複合体の測定値から検量線を作成し、
前記検量線及び前記IgA凝集体の測定値に基づいて、前記試料中のIgA凝集体の濃度を取得する請求項8に記載の方法。 - 前記レクチンが固相に固定されている請求項5~9のいずれか1項に記載の方法。
- 前記IgAがIgA1である請求項5~10のいずれか1項に記載の方法。
- 前記レクチンが、WFA、HHL、GNA、NPA、SBA、VVA、BPL、TJA-II、PHA-L及びAOLからなる群から選択される少なくとも1のレクチンである請求項5~11のいずれか1項に記載の方法。
- 前記レクチンがWFAである請求項5~12のいずれか1項に記載の方法。
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WO2013172347A1 (ja) | 2012-05-14 | 2013-11-21 | 独立行政法人産業技術総合研究所 | IgA凝集体の検出方法およびIgA腎症の検査方法 |
JP2015502968A (ja) | 2011-12-23 | 2015-01-29 | フォルシュングスツェントルム ユーリッヒ ゲゼルシャフト ミット ベシュレンクテル ハフツングForschungszentrum Juelich GmbH | 生体固有のタンパク質からの病原性の凝集体を定量化するための標準物質 |
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US20120172247A1 (en) | 2009-07-14 | 2012-07-05 | Hisashi Narimatsu | Method for measuring glycoprotein, method for examining liver disease, reagent for quantitative determination of glycoprotein, and glycan-marker glycoprotein as an index for clinical conditions of liver disease |
JP2015502968A (ja) | 2011-12-23 | 2015-01-29 | フォルシュングスツェントルム ユーリッヒ ゲゼルシャフト ミット ベシュレンクテル ハフツングForschungszentrum Juelich GmbH | 生体固有のタンパク質からの病原性の凝集体を定量化するための標準物質 |
WO2013172347A1 (ja) | 2012-05-14 | 2013-11-21 | 独立行政法人産業技術総合研究所 | IgA凝集体の検出方法およびIgA腎症の検査方法 |
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