Improved procedures for purification of the Bandeiraea simplicifolia I isolectins and Bandeiraea simplicifolia II lectin by affinity chromatography.
Improved procedures for purification of the Bandeiraea simplicifolia I isolectins and Bandeiraea simplicifolia II lectin by affinity chromatography.
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改进了通过亲和层析纯化 Bandeiraea simplicifolia I 同种凝集素和 Bandeiraea simplicifolia II 凝集素的程序。
DOI:
10.1111/j.1432-1033.1980.tb07197.x
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发表时间:
1980
期刊:
影响因子:
--
通讯作者:
Goldstein,IJ
中科院分区:
文献类型:
--
作者:
Delmotte,FM;Goldstein,IJ
Bandeiraea simplicifoliaplant seeds contain a family of five α‐d‐gal actopyranosyl‐binding isolectins (BS I‐A4, A3B, A2B2, AB3, B4) andN‐acetyl‐d‐glucosamine‐binding lectin (BS II). After Pi/NaCl extraction and ammonium sulfate fractionation BS II is specifically adsorbed ontop‐aninobenzyl‐1‐thio‐N‐acetyl‐β‐d‐glucosaminide‐succinylaminohexylaminyl—Sepharose‐4B. The BS I isolectins pass through this column and BS II is selectively eluted by Pi/NaCl containing 2 mMN‐acetyl‐d‐glucosamine or by 0.1 M sodium acetate buffer pH 3.6. The material not bound to the column is loaded ontop‐aminophenyl‐β‐d‐galactopyranosyl‐succinylaminohexylaminyl—Sepharose 4B. BS I‐A4is specifically eluted in a sharp peak with Pi/NaCl containing 1 mMN‐acetyl‐d‐galactosamine. Then, BS I‐A3B, A2B2, AB3and B4are selectively eluted, in a single peak for each isolectin, with Pi/NaCl containing 3 mM, 8 mM, 15 mM and 50 mM methyl α‐d‐galactopyranoside, respectively.