Department of Biomolecular Sciences, Weizmann Institute of Science, Rehovot, Israel.
Life Sciences Core Facilities, Weizmann Institute of Science, Rehovot, Israel.
Life Sci Alliance. 2023 Jul 17;6(10). doi: 10.26508/lsa.202201634. Print 2023 Oct.
Protein degradation is one of the essential mechanisms that enables reshaping of the proteome landscape in response to various stimuli. The largest E3 ubiquitin ligase family that targets proteins to degradation by catalyzing ubiquitination is the cullin-RING ligases (CRLs). Many of the proteins that are regulated by CRLs are central to tumorigenesis and tumor progression, and dysregulation of the CRL family is frequently associated with cancer. The CRL family comprises ∼300 complexes, all of which are regulated by the COP9 signalosome complex (CSN). Therefore, CSN is considered an attractive target for therapeutic intervention. Research efforts for targeted CSN inhibition have been directed towards inhibition of the complex enzymatic subunit, CSN5. Here, we have taken a fresh approach focusing on CSNAP, the smallest CSN subunit. Our results show that the C-terminal region of CSNAP is tightly packed within the CSN complex, in a groove formed by CSN3 and CSN8. We show that a 16 amino acid C-terminal peptide, derived from this CSN-interacting region, can displace the endogenous CSNAP subunit from the complex. This, in turn, leads to a CSNAP null phenotype that attenuates CSN activity and consequently CRLs function. Overall, our findings emphasize the potential of a CSNAP-based peptide for CSN inhibition as a new therapeutic avenue.
蛋白质降解是一种重要的机制,能够响应各种刺激重塑蛋白质组景观。靶向蛋白质降解的最大 E3 泛素连接酶家族是 cullin-RING 连接酶 (CRLs)。许多受 CRL 调节的蛋白质是肿瘤发生和肿瘤进展的核心,CRL 家族的失调常与癌症有关。CRL 家族包括约 300 个复合物,所有这些复合物都受 COP9 信号体复合物 (CSN) 的调节。因此,CSN 被认为是治疗干预的一个有吸引力的靶点。针对 CSN 抑制的靶向研究努力集中在抑制复杂的酶亚基 CSN5 上。在这里,我们采取了一种新的方法,专注于 CSNAP,这是 CSN 中最小的亚基。我们的结果表明,CSNAP 的 C 末端区域在 CSN 复合物中紧密包装,位于 CSN3 和 CSN8 形成的凹槽中。我们表明,来自该 CSN 相互作用区域的 16 个氨基酸 C 末端肽可以将内源性 CSNAP 亚基从复合物中置换出来。这反过来又导致 CSNAP 缺失表型,削弱了 CSN 活性,从而影响了 CRL 的功能。总的来说,我们的研究结果强调了基于 CSNAP 的肽作为一种新的治疗途径抑制 CSN 的潜力。