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本文引用的文献

1
Catalytic metallodrugs based on the LaR2C peptide target HCV SLIV IRES RNA.基于LaR2C肽的催化金属药物靶向丙型肝炎病毒(HCV)SLIV IRES RNA。
Dalton Trans. 2015 Dec 28;44(48):20972-82. doi: 10.1039/c5dt02837j. Epub 2015 Nov 19.
2
Toward Efficient Enzymes for the Generation of Universal Blood through Structure-Guided Directed Evolution.通过结构导向的定向进化生成通用血液的高效酶。
J Am Chem Soc. 2015 May 6;137(17):5695-705. doi: 10.1021/ja5116088. Epub 2015 Apr 24.
3
Toward the design of a catalytic metallodrug: selective cleavage of G-quadruplex telomeric DNA by an anticancer copper-acridine-ATCUN complex.迈向催化金属药物的设计:一种抗癌铜-吖啶-ATCUN配合物对G-四链体端粒DNA的选择性切割
Angew Chem Int Ed Engl. 2015 Feb 2;54(6):1901-5. doi: 10.1002/anie.201410434. Epub 2014 Dec 11.
4
Inactivation of sortase A mediated by metal ATCUN complexes.由金属ATCUN配合物介导的分选酶A失活
J Biol Inorg Chem. 2014 Dec;19(8):1327-39. doi: 10.1007/s00775-014-1190-x. Epub 2014 Sep 9.
5
Structure and substrate specificity of a eukaryotic fucosidase from Fusarium graminearum.禾谷镰刀菌真核岩藻糖苷酶的结构与底物特异性
J Biol Chem. 2014 Sep 12;289(37):25624-38. doi: 10.1074/jbc.M114.583286. Epub 2014 Aug 1.
6
Insight into the recognition, binding, and reactivity of catalytic metallodrugs targeting stem loop IIb of hepatitis C IRES RNA.深入了解靶向丙型肝炎病毒内部核糖体进入位点(IRES)RNA茎环IIb的催化金属药物的识别、结合和反应活性。
ChemMedChem. 2014 Jun;9(6):1275-85. doi: 10.1002/cmdc.201400070. Epub 2014 Apr 22.
7
Transfusion reaction in a case with the rare Bombay blood group.一例罕见孟买血型患者的输血反应。
Asian J Transfus Sci. 2013 Jan;7(1):86-7. doi: 10.4103/0973-6247.106754.
8
Differences in the substrate specificities and active-site structures of two α-L-fucosidases (glycoside hydrolase family 29) from Bacteroides thetaiotaomicron.来自多形拟杆菌的两种α-L-岩藻糖苷酶(糖苷水解酶家族29)在底物特异性和活性位点结构上的差异。
Biosci Biotechnol Biochem. 2012;76(5):1022-4. doi: 10.1271/bbb.111004. Epub 2012 May 7.
9
Identification of a rare blood group, "Bombay (Oh) phenotype," in Bhuyan tribe of Northwestern Orissa, India.在印度奥里萨邦西北部的布扬部落中发现一种罕见血型“孟买(Oh)血型”。
Indian J Hum Genet. 2007 Sep;13(3):109-13. doi: 10.4103/0971-6866.38985.
10
Utilization of natural fucosylated oligosaccharides by three novel alpha-L-fucosidases from a probiotic Lactobacillus casei strain.新型益生菌干酪乳杆菌来源的α-L-岩藻糖苷酶对天然岩藻糖基化低聚糖的利用
Appl Environ Microbiol. 2011 Jan;77(2):703-5. doi: 10.1128/AEM.01906-10. Epub 2010 Nov 19.

人工糖苷酶的设计:从人红细胞中去除 H 抗原的金属肽。

Design of Artificial Glycosidases: Metallopeptides that Remove H Antigen from Human Erythrocytes.

机构信息

Department of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, OH, 43210, USA.

出版信息

Angew Chem Int Ed Engl. 2017 Mar 1;56(10):2763-2766. doi: 10.1002/anie.201612079. Epub 2017 Jan 27.

DOI:10.1002/anie.201612079
PMID:28128528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5455340/
Abstract

Catalysts that promote carbohydrate degradation have a wide range of potential applications, but the use of either enzyme glycosidases or small-molecule catalysts in biological systems raises significant challenges. Herein, we demonstrate a novel strategy for the design of synthetic agents that mimic natural glycosidases and address current problems for biological use. This strategy is illustrated by application to the development of potential blood substitutes for the rare Bombay blood type that is characterized by a deficiency of H2 antigen. Metallopeptides with 16 to 20 amino acids were constructed as artificial fucosidases that exhibit selective carbohydrate cleavage reactivity toward l-fucose over d-glucose. Selective fucose cleavage from the H2-antigen saccharide enables efficient removal of H2 antigen from erythrocytes and thereby accomplishes the conversion of regular human type-O blood into a potential blood substitute for the rare Bombay blood type.

摘要

促进碳水化合物降解的催化剂具有广泛的潜在应用,但在生物系统中使用酶糖苷酶或小分子催化剂会带来重大挑战。在此,我们展示了一种设计模拟天然糖苷酶的合成试剂的新策略,并解决了生物应用中的当前问题。该策略通过应用于开发罕见的孟买血型的潜在血液替代品得到了说明,这种血型的特征是缺乏 H2 抗原。构建了具有 16 至 20 个氨基酸的金属肽作为人工岩藻糖苷酶,其对 l-岩藻糖相对于 d-葡萄糖表现出选择性的碳水化合物切割反应性。从 H2 抗原糖中选择性切割岩藻糖可有效地从红细胞中去除 H2 抗原,从而将常规的人类 O 型血转化为罕见的孟买血型的潜在血液替代品。