Griffith I J, Smith P M, Pollock J, Theerakulpisut P, Avjioglu A, Davies S, Hough T, Singh M B, Simpson R J, Ward L D
ImmuLogic Pharmaceutical Corporation, Cambridge, MA 02139.
FEBS Lett. 1991 Feb 25;279(2):210-5. doi: 10.1016/0014-5793(91)80151-r.
We have isolated a full length cDNA clone encoding the major glycoprotein allergen Lol pI. The clone was selected using a combination of immunological screening of a cDNA expression library and PCR amplification of Lol pI-specific transcripts. Lol pI expressed in bacteria as a fusion protein shows recognition by specific IgE antibodies present in sera of grass pollen-allergic subjects. Northern analysis has shown that the Lol pI transcripts are expressed only in pollen of rye-grass. Molecular cloning of Lol pI provides a molecular genetic approach to study the structure-function relationship of allergens.
我们分离出了一个编码主要糖蛋白过敏原黑麦草花粉变应原I(Lol pI)的全长cDNA克隆。该克隆是通过对cDNA表达文库进行免疫筛选和对Lol pI特异性转录本进行PCR扩增相结合的方法筛选出来的。在细菌中作为融合蛋白表达的Lol pI可被草花粉过敏患者血清中的特异性IgE抗体识别。Northern分析表明,Lol pI转录本仅在黑麦草花粉中表达。Lol pI的分子克隆为研究过敏原的结构-功能关系提供了一种分子遗传学方法。