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脂肪族二羧酸的双磺基琥珀酰亚胺酯:一类新型的血红蛋白A的“亲和定向”β-β交联剂。

Bissulfosuccinimidyl esters of aliphatic dicarboxylic acids: a new class of 'affinity directed' beta beta crosslinkers of HbA.

作者信息

Manjula B N, Roy R P, Smith P K, Acharya A S

机构信息

Division of Hematology, Albert Einstein College of Medicine, Bronx, NY.

出版信息

Artif Cells Blood Substit Immobil Biotechnol. 1994;22(3):747-52. doi: 10.3109/10731199409117907.

Abstract

The potential of sulfosuccinimidyl ester of suberic acid as an intramolecular crosslinker of HbA, directed to the positive charge rich domain of the protein (DPG pocket) has been investigated. The suberate ester introduced crosslinks between the beta-chains and inhibited the dissociation of HbA into alpha beta dimers. The facile crosslinking reaction seen with this suberate ester as compared to the absence of crosslinking with the diaspirin derivative of suberic acid suggests the strong 'steering' influence of the sulfosuccinimidyl moiety of the reagent to the targeted site. The application of this crosslinking approach in the preparation of Hb based blood substitutes is discussed.

摘要

已对辛二酸磺基琥珀酰亚胺酯作为血红蛋白A(HbA)分子内交联剂的潜力进行了研究,该交联剂作用于蛋白质富含正电荷的区域(二磷酸甘油酸口袋)。辛二酸酯在β链之间引入交联,并抑制HbA解离成αβ二聚体。与辛二酸二阿司匹林衍生物不存在交联相比,这种辛二酸酯观察到的容易交联反应表明该试剂的磺基琥珀酰亚胺部分对靶向位点有很强的“导向”影响。讨论了这种交联方法在制备基于血红蛋白的血液替代品中的应用。

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