trna synthetase 中文意思是什麼

trna synthetase 解釋
trna合成酶
  1. Polymyositis ( pm ) and dermatoyositis ( dm ), devastating inflammatory muscle diseases, are associated with the myositis - specific anti - jo - 1 autoantibody, found in 25 - 40 % of such patients. anti - jo - 1 antibodies react with histidyl - trna synthetase

    抗組氨酰? trna合成酶抗體,臨床上又稱抗jo - 1抗體,是診斷這類疾病的標志性抗體。
  2. A page gel, stained by the petiodic acid - schiff ' s method to reveal glycoproteins, further displayed that the bindng - protein was a glycoprotein belonging to lectin, which contained 17. 4 % ( w / w ) neutral carbohydrate content of the glycoprotein detected by the phenol / h2so4 method. peptide mapping was comparable to the reported protein in protein bank. the database homology search ( ncbi blast ) indicated that the binding - protein shared 70 - 80 % homogeneity to l - aspartate oxidase, aspartyl / glutamyl - trna ( asn / gln ) amidotransferase subunit b, glutamyl - trna reductase, histidyl - trna synthetase

    連續梯度聚丙烯耽胺凝膠電泳、 sds一聚丙烯酞胺凝膠電泳和等電聚焦的結果表明該蛋白分子量為1 「 . skda ,由二個相同的亞基組成,亞基分子量為」 . ikda ,等電點為8 . 25 .糖蛋白染色結合考馬斯亮藍染色的結果證實此結合蛋白是個糖蛋白,其中糖含量為17 . 44 % ,蛋白含量為82 . 56 % .凝集反應確定該糖蛋白也是一個凝集素
  3. Hisityl - trna synthetase catalyzes the aminoacylation of trnahis in the initial step of protein biosynthesis. the involumen of histidyl - trna synthetase in autoimmune diseases is another feature of the enzyme. in studies, it is reported that purified jo - 1 antigen can increase the detection rate of anti - jo - 1 antibody. but it is difficult to obtain a single component by biochemical extraction. genetic engineering can help us to desolve this problem. after looking up mrna sequence encoding histidyl - trna synthetase in genebank, we used rt - pcr technology to gain its full length dna sequence. the vestor ptybllwas used in the construction of expressing vestor. we transformed the jo - 1 gene into er2566 and used this system to express fusion jo - 1 antigen

    本實驗從人胎盤中提取總rna ,利用rt - pcr技術獲得了編碼jo - 1的基因整長序列,選用impact - cn系統中的ptyb11載體,構建了jo - 1基因的克隆與表達載體,並轉化大腸桿菌er2566 ,經過抗性篩選、分子量大小比較、雙酶切鑒定、和pcr鑒定等多種方法驗證,篩選出了5個陽性克隆。
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