Lima Maria Carolina P, Hornsby Braxten D, Lim Carol S, Cheatham Thomas E
Department of Medicinal Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
Department of Molecular Pharmaceutics, University of Utah, Salt Lake City, Utah 84112, United States.
bioRxiv. 2023 Nov 17:2023.11.15.566894. doi: 10.1101/2023.11.15.566894.
The chimeric oncoprotein Bcr-Abl is the causative agent of virtually all chronic myeloid leukemias (CML) and a subset of acute lymphoblastic leukemias (ALL). As a result of the so-called Philadelphia Chromosome translocation t(9;22), Bcr-Abl manifests as a constitutively active tyrosine kinase which promotes leukemogenesis by activation of cell cycle signaling pathways. Constitutive and oncogenic activation is mediated by an N-terminal coiled-coil oligomerization domain in Bcr (Bcr-CC), presenting a therapeutic target for inhibition of Bcr-Abl activity toward the treatment of Bcr-Abl+ leukemias. Previously, we demonstrated that a rationally designed Bcr-CC mutant, CCmut3, exerts a dominant negative effect upon Bcr-Abl activity by preferential oligomerization with Bcr-CC. Moreover, we have shown conjugation to a leukemia-specific cell-penetrating peptide (CPP-CCmut3) improves intracellular delivery and activity. However, our full-length CPP-CCmut3 construct (81 aa) is encumbered by an intrinsically high degree of conformational variability and susceptibility to proteolytic degradation, relative to traditional small molecule therapeutics. Here, we iterate a new generation of our inhibitor against Bcr-CC mediated Bcr-Abl assembly that is designed to address these constraints through incorporation of all-hydrocarbon staples spanning i, i + 7 positions in helix α2 (CPP-CCmut3-st). We utilize computational modeling and biomolecular simulation to design and characterize single and double staple candidates in silico, evaluating binding energetics and building upon our seminal work modeling single hydrocarbon staples when applied to a truncated Bcr-CC sequence. This strategy enables us to efficiently build, characterize, and screen lead single/double stapled CPP-CCmut3-st candidates for experimental studies and validation in vitro and in vivo. In addition to full-length CPP-CCmut, we model a truncated system characterized by deletion of helix α1 and the flexible-loop linker, which are known to impart high conformational variability. To study the impact of the N-terminal cyclic CPP toward model stability and inhibitor activity, we also model the full-length and truncated systems without CPP, with cyclized CPP, and with linear CPP, for a total of six systems which comprise our library. From this library, we present lead stapled peptide candidates to be synthesized and evaluated experimentally as our next-generation inhibitors against Bcr-Abl.
嵌合癌蛋白Bcr-Abl实际上是所有慢性髓性白血病(CML)以及一部分急性淋巴细胞白血病(ALL)的致病因子。由于所谓的费城染色体易位t(9;22),Bcr-Abl表现为一种组成型活性酪氨酸激酶,它通过激活细胞周期信号通路来促进白血病发生。组成型和致癌性激活由Bcr中的N端卷曲螺旋寡聚化结构域(Bcr-CC)介导,这为抑制Bcr-Abl活性以治疗Bcr-Abl+白血病提供了一个治疗靶点。此前,我们证明了一个经过合理设计的Bcr-CC突变体CCmut3,通过与Bcr-CC优先寡聚化,对Bcr-Abl活性发挥显性负效应。此外,我们还表明与白血病特异性细胞穿透肽(CPP-CCmut3)偶联可改善细胞内递送和活性。然而,相对于传统小分子疗法,我们的全长CPP-CCmut3构建体(81个氨基酸)存在固有高度的构象变异性和对蛋白水解降解的敏感性。在此,我们迭代了新一代针对Bcr-CC介导的Bcr-Abl组装的抑制剂,其设计目的是通过在α2螺旋的i、i + 7位置引入全碳氢钉来解决这些限制(CPP-CCmut3-st)。我们利用计算建模和生物分子模拟在计算机上设计和表征单钉和双钉候选物,评估结合能,并基于我们在将单碳氢钉应用于截短的Bcr-CC序列时的开创性工作。这种策略使我们能够高效地构建、表征和筛选用于实验研究以及体外和体内验证的先导单/双钉CPP-CCmut3-st候选物。除了全长CPP-CCmut,我们还对一个截短系统进行建模,该系统的特征是缺失已知会导致高度构象变异性的α1螺旋和柔性环连接子。为了研究N端环状CPP对模型稳定性和抑制剂活性的影响,我们还对不含CPP、含环化CPP和线性CPP的全长和截短系统进行建模,总共六个系统构成了我们的文库。从这个文库中,我们展示了先导钉肽候选物,它们将被合成并通过实验评估,作为我们针对Bcr-Abl的下一代抑制剂。