Scian Michele, Guttman Miklos, Bouldin Samantha D, Outten Caryn E, Atkins William M
Department of Medicinal Chemistry, University of Washington , Box 357610, Seattle, Washington 98195-7610, United States.
Department of Chemistry and Biochemistry, University of South Carolina , Columbia, South Carolina 29208, United States.
Biochemistry. 2016 Aug 23;55(33):4720-30. doi: 10.1021/acs.biochem.6b00622. Epub 2016 Aug 11.
The myeloablative agent busulfan (1,4-butanediol dimethanesulfonate) is an old drug that is used routinely to eliminate cancerous bone marrow prior to hematopoietic stem cell transplant. The myeloablative activity and systemic toxicity of busulfan have been ascribed to its ability to cross-link DNA. In contrast, here we demonstrate that incubation of busulfan with the thiol redox proteins glutaredoxin or thioredoxin at pH 7.4 and 37 °C results in the formation of putative S-tetrahydrothiophenium adducts at their catalytic Cys residues, followed by β-elimination to yield dehydroalanine. Both proteins contain a second Cys, in their catalytic C-X-X-C motif, which reacts with the dehydroalanine, the initial Cys adduct with busulfan, or the S-tetrahydrothiophenium, to form novel intramolecular cross-links. The reactivity of the dehydroalanine (DHA) formed is further demonstrated by adduction with glutathione to yield a lanthionine and by a novel reaction with the reducing agent tris(2-carboxyethyl)phosphine (TCEP), which yields a phosphine adduct via Michael addition to the DHA. Formation of a second quaternary organophosphonium salt via nucleophilic substitution with TCEP on the initial busulfan-protein adduct or on the THT(+)-Redoxin species is also observed. These results reveal a rich potential for reactions of busulfan with proteins in vitro, and likely in vivo. It is striking that several of the chemically altered protein products retain none of the atoms of busulfan, in contrast to typical drug-protein adducts or traditional protein modification reagents. In particular, the ability of a clinically used drug to convert Cys to dehydrolanine in intact proteins, and its subsequent reaction with biological thiols, is unprecedented.
清髓性药物白消安(1,4 - 丁二醇二甲磺酸酯)是一种老药,常用于在造血干细胞移植前清除癌性骨髓。白消安的清髓活性和全身毒性归因于其交联DNA的能力。相比之下,我们在此证明,在pH 7.4和37°C条件下,白消安与硫醇氧化还原蛋白谷氧还蛋白或硫氧还蛋白孵育,会在其催化性半胱氨酸残基处形成推定的S - 四氢噻吩鎓加合物,随后发生β消除反应生成脱氢丙氨酸。这两种蛋白质在其催化性C - X - X - C基序中都含有第二个半胱氨酸,它会与脱氢丙氨酸、最初与白消安形成的半胱氨酸加合物或S - 四氢噻吩鎓反应,形成新型分子内交联。通过与谷胱甘肽加合生成羊毛硫氨酸以及与还原剂三(2 - 羧乙基)膦(TCEP)发生新型反应进一步证明了所形成的脱氢丙氨酸(DHA)的反应活性,后者通过迈克尔加成反应与DHA生成膦加合物。还观察到通过TCEP对最初的白消安 - 蛋白质加合物或THT(+) - 氧化还原蛋白物种进行亲核取代形成第二种季鏻盐。这些结果揭示了白消安在体外以及可能在体内与蛋白质发生反应的丰富潜力。令人惊讶的是,与典型的药物 - 蛋白质加合物或传统蛋白质修饰试剂相比,几种化学改变的蛋白质产物都不保留白消安的任何原子。特别是,一种临床使用的药物能够在完整蛋白质中将半胱氨酸转化为脱氢丙氨酸,并随后与生物硫醇发生反应,这是前所未有的。