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使用星爆型聚酰胺-胺(PAMAM)树枝状大分子合成新型聚合物结合的腺嘌呤核苷酸。

Synthesis of new polymer-bound adenine nucleotides using starburst PAMAM dendrimers.

作者信息

Abdelmoez Wael, Yasuda Masahiro, Ogino Hiroyasu, Ishimi Kosaku, Ishikawa Haruo

机构信息

Department of Chemical Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Sakai, Osaka 599-8531, Japan.

出版信息

Biotechnol Prog. 2002 Jul-Aug;18(4):706-12. doi: 10.1021/bp020062o.

Abstract

Two types of new polymer-bound adenine nucleotides were synthesized by coupling adenine nucleotides (ATP and ADP) with starburst polyamidoamine (PAMAM) dendrimers. The first type was obtained by coupling native adenine nucleotides directly with a carboxy-terminated PAMAM dendrimer. In the second type, the nucleotides were modified by introducing a spacer arm containing a carboxylic end group (N(6)-R-ATP and N(6)-R-ADP) and coupled with an amine-terminated PAMAM dendrimer. Both types of the dendrimers were coupled with native or the modified nucleotides using the well-known carbodiimide activation technique. The optimum coupling pH and temperature were 4 and 30 degrees C, respectively, for preparing the carboxy-terminated PAMAM-bound ATP or ADP, and were 9 and 50 degrees C, respectively, for preparing the amine-terminated PAMAM-bound N(6)-R-ATP or N(6)-R-ADP. The ATP or ADP contents in the synthesized polymers were found to be 4 mol of ATP or of ADP/mol of carboxy-terminated PAMAM-bound ATP or ADP and 25 mol of ATP or of ADP/mol of amine-terminated PAMAM-bound N(6)-R-ATP or N(6)-R-ADP. The coenzymatic activities relative to the native ATP of the carboxy-terminated PAMAM-bound ATP against glucokinase and hexokinase were 16 and 7%, respectively, and those of the amine-terminated PAMAM-bound N(6)-R-ATP 2 and 1%, respectively. The coenzymatic activities relative to the native ADP of the carboxy-terminated PAMAM-bound ADP and the amine-terminated PAMAM-bound N(6)-R-ADP against acetate kinase were 24 and 3.5%, respectively.

摘要

通过将腺嘌呤核苷酸(ATP和ADP)与星状聚酰胺胺(PAMAM)树枝状大分子偶联,合成了两种新型的聚合物结合腺嘌呤核苷酸。第一种是通过将天然腺嘌呤核苷酸直接与羧基末端的PAMAM树枝状大分子偶联得到的。第二种类型中,核苷酸通过引入含有羧基端基的间隔臂(N(6)-R-ATP和N(6)-R-ADP)进行修饰,并与胺基末端的PAMAM树枝状大分子偶联。两种类型的树枝状大分子均使用著名的碳二亚胺活化技术与天然或修饰的核苷酸偶联。制备羧基末端PAMAM结合的ATP或ADP时,最佳偶联pH和温度分别为4和30℃,而制备胺基末端PAMAM结合的N(6)-R-ATP或N(6)-R-ADP时,最佳偶联pH和温度分别为9和50℃。发现合成聚合物中ATP或ADP的含量分别为4摩尔ATP或ADP/摩尔羧基末端PAMAM结合的ATP或ADP以及25摩尔ATP或ADP/摩尔胺基末端PAMAM结合的N(6)-R-ATP或N(6)-R-ADP。羧基末端PAMAM结合的ATP相对于天然ATP对葡萄糖激酶和己糖激酶的辅酶活性分别为16%和7%,胺基末端PAMAM结合的N(6)-R-ATP的辅酶活性分别为2%和1%。羧基末端PAMAM结合的ADP和胺基末端PAMAM结合的N(6)-R-ADP相对于天然ADP对乙酸激酶的辅酶活性分别为24%和3.5%。

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