摘要
淋巴特异性酪氨酸磷酸酶(lymphoid-specific tyrosine phosphatase,LYP)主要分布于淋巴系统,是由PTPn22基因编码的非受体蛋白酪氨酸磷酸酶。正常生理条件下,该酶与CSK结合后,可抑制T细胞受体信号传导并维持免疫系统自身稳定。病理条件下,该酶会发生突变而无法正常结合CSK,导致其功能亢进并诱发各种免疫疾病。因此淋巴特异性酪氨酸磷酸酶也被认为是治疗I型糖尿病、风湿性关节炎以及格雷夫斯病等自身免疫疾病的新型靶标。本文将综述其研究进展,并总结已报道的抑制剂的结构类型及活性。
Lymphoid-specific tyrosine phosphatase (LYP) is a phosphatase that is encoded by protein tyrosine phosphatase non-receptor type 22 and is mainly distributed in lymphoid. In psychological condition, LYP inhibits T-cell receptor (TCR) signaling in association with C-terminal kinase (CSK). While in pathological condition, mutant LYP dissociates with CSK, which augments the inhibition of TCR signaling and leads to autoimmune diseases. Consequently, LYP is now considered as a new target of type I diabetes, rheumatic arthritis and Graves disease and some other autoimmune disorders. This review mainly focuses on the development of LYP inhibitors in their structures and activities.
出处
《药学学报》
CAS
CSCD
北大核心
2017年第5期699-705,共7页
Acta Pharmaceutica Sinica
基金
山东省自然科学基金杰出青年基金资助项目(JQ201319)
山东大学自主创新基金资助项目(2016JC018)