Manjula B N, Smith P K, Malavalli A, Acharya A S
Division of Hematology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Artif Cells Blood Substit Immobil Biotechnol. 1995;23(3):311-8. doi: 10.3109/10731199509117947.
The sulfosuccinimidyl esters of suberic and sebacic acids readily introduce intramolecular crosslinks into oxy HbA at pH 7.4, the relative efficiency of crosslinking by the suberate ester being slightly higher than that of sebacate. Nearly quantitative intramolecular crosslinking of HbA (0.5 mM) is achieved at pH 7.4 and 4 degrees C by using 5 and 10 fold molar excess of the suberic and sebacic acid, respectively. In contrast to the facile crosslinking reaction seen with the bis sulfosuccinimidyl sebacate, bis sulfosuccinimidyl sebacate and bis (3:5 dibromo salicyl) sebacate did not introduce any crosslinking into HbA despite the fact that the 'crosslinking arm' of the two bifunctional reagents is the same. The discrepant reactivity of the two reagents demonstrates the 'steering' influence of the negative charge of the leaving group of the reagent, namely sulfo succinimidyl moiety to specific domains of HbA rich in positively charged groups. A second advantage is also anticipated in the use of the sulfosuccinimidyl esters of aliphatic dicarboxylic acids. We speculate that the intermediate in the crosslinking reaction mimics the structural aspects of the low oxygen affinity 'psuedo crosslinked Hb'. Conversion of the low oxygen affinity 'psuedocrosslinked Hb' into crosslinked Hb by the formation of the second isopeptide bond may lead to the 'freezing in' of the elements of low oxygen affinity structure. Consistent with this speculation, the suberate crosslinked Hb indeed exhibited low oxygen affinity even though the crosslinking reaction was carried out in the oxy state.(ABSTRACT TRUNCATED AT 250 WORDS)
辛二酸和癸二酸的磺基琥珀酰亚胺酯在pH 7.4时能轻易地将分子内交联引入氧合血红蛋白A(HbA)中,辛二酸酯的交联相对效率略高于癸二酸酯。在pH 7.4和4℃条件下,分别使用5倍和10倍摩尔过量的辛二酸和癸二酸,可实现HbA(0.5 mM)近乎定量的分子内交联。与双磺基琥珀酰亚胺基癸二酸酯所见的容易的交联反应相反,双磺基琥珀酰亚胺基癸二酸酯和双(3:5 - 二溴水杨基)癸二酸酯尽管两种双功能试剂的“交联臂”相同,但并未将任何交联引入HbA中。两种试剂不同的反应活性证明了试剂离去基团(即磺基琥珀酰亚胺部分)的负电荷对富含带正电荷基团的HbA特定结构域的“导向”影响。在使用脂肪族二羧酸的磺基琥珀酰亚胺酯时还预期有第二个优点。我们推测交联反应中的中间体模拟了低氧亲和力“假交联Hb”的结构特征。通过形成第二个异肽键将低氧亲和力“假交联Hb”转化为交联Hb可能导致低氧亲和力结构元素的“固定”。与这一推测一致,辛二酸酯交联的Hb即使在氧合状态下进行交联反应,确实表现出低氧亲和力。(摘要截短至250字)