Heinlein C A, Chang C
Department of Pathology, University of Rochester, NY, USA.
Endocrine. 2001 Mar;14(2):143-9. doi: 10.1385/ENDO:14:2:143.
Molecular chaperones assist proteins to reach their mature and functional conformation. It has become apparent in recent years that chaperones function as part of a multiprotein heterocomplex that is potentially involved not only in protein folding, but also in intracellular trafficking and in targeting proteins for degradation. In the case of steroid receptors, the activity of the chaperone heterocomplex, as well as the proteins comprising the heterocomplex, has an effect on the observed ligand-dependent transcriptional activity of the receptor. The direct interaction between chaperones and steroid receptors makes them potential therapeutic targets in a number of pathologic conditions. In the case of cancers with steroid receptor involvement, such as breast and prostate cancer, the inhibition of chaperone activity may inhibit tumor cell growth. Conversely, enhancement of chaperone activity may be beneficial in disorders of protein misfolding, as in the case of androgen receptor aggregates found in Spinal and Bulbar Muscular Atrophy.
分子伴侣协助蛋白质达到其成熟且具有功能的构象。近年来已变得明显的是,伴侣蛋白作为多蛋白异源复合物的一部分发挥作用,该复合物不仅可能参与蛋白质折叠,还参与细胞内运输以及将蛋白质靶向降解。就类固醇受体而言,伴侣蛋白异源复合物的活性以及构成该异源复合物的蛋白质,会对所观察到的受体的配体依赖性转录活性产生影响。伴侣蛋白与类固醇受体之间的直接相互作用使其成为多种病理状况下潜在的治疗靶点。在涉及类固醇受体的癌症(如乳腺癌和前列腺癌)中,抑制伴侣蛋白活性可能会抑制肿瘤细胞生长。相反,增强伴侣蛋白活性可能对蛋白质错误折叠的疾病有益,如在脊髓延髓肌肉萎缩症中发现的雄激素受体聚集体的情况。