Khan Asra Nasir, Khan Rizwan Hasan
Interdisciplinary Biotechnology Unit, AMU, Aligarh 202002, India.
Interdisciplinary Biotechnology Unit, AMU, Aligarh 202002, India.
Int J Biol Macromol. 2022 Dec 31;223(Pt A):143-160. doi: 10.1016/j.ijbiomac.2022.11.031. Epub 2022 Nov 8.
Most of the cell's chemical reactions and structural components are facilitated by proteins. But proteins are highly dynamic molecules, where numerous modifications or changes in the cellular environment can affect their native conformational fold leading to protein aggregation. Various stress conditions, such as oxidative stress, mutations and metal toxicity may cause protein misfolding and aggregation by shifting the conformational equilibrium towards more aggregation-prone states. Most of the protein misfolding diseases (PMDs) involve aggregation of protein. We have discussed such proteins like Aβ peptide, α-synuclein, amylin and lysozyme involved in Alzheimer's, Parkinson's, type II diabetes and non-neuropathic systemic amyloidosis respectively. Till date, all advances in PMDs therapeutics help symptomatically but do not prevent the root cause of the disease, i.e., the aggregation of protein involved in the diseases. Current efforts focused on developing therapies for PMDs have employed diverse strategies; repositioning pre-existing drugs as it saves time and money; natural compounds that are touted as potential drug candidates have an advantage of being taken in diet normally and will induce lesser side effects. This review also covers recently developed therapeutic strategies like antisense drugs and disaggregases which has yielded therapeutic agents that have transitioned from preclinical studies into human clinical trials.
细胞的大多数化学反应和结构成分都由蛋白质促成。但蛋白质是高度动态的分子,细胞环境中的众多修饰或变化会影响其天然构象折叠,导致蛋白质聚集。各种应激条件,如氧化应激、突变和金属毒性,可能通过将构象平衡向更易聚集的状态转移而导致蛋白质错误折叠和聚集。大多数蛋白质错误折叠疾病(PMD)都涉及蛋白质聚集。我们已经讨论了分别参与阿尔茨海默病、帕金森病、II型糖尿病和非神经性系统性淀粉样变性的Aβ肽、α-突触核蛋白、胰淀素和溶菌酶等蛋白质。迄今为止,PMD治疗学的所有进展都只是缓解症状,而不能预防疾病的根本原因,即疾病中涉及的蛋白质聚集。目前致力于开发PMD治疗方法的努力采用了多种策略;重新利用现有药物,因为这样省时省钱;被吹捧为潜在候选药物的天然化合物具有通常可通过饮食摄入且副作用较小的优势。本综述还涵盖了最近开发的治疗策略,如反义药物和解聚酶,这些策略已经产生了从临床前研究过渡到人体临床试验的治疗药物。