Department of Chemistry, Wesleyan University , Lawn Avenue, Middletown, Connecticut 06459, United States.
Biochemistry. 2013 May 28;52(21):3712-20. doi: 10.1021/bi4003887. Epub 2013 May 16.
The effectiveness of β-lactam antibiotics is greatly limited by the ability of bacteria to produce β-lactamases. These enzymes catalyze the hydrolysis of β-lactams and thus loss of their antibiotic activity. The search for inhibitors of β-lactamases began soon after β-lactams were introduced into medical practice and continues today. Some time ago, we introduced a new class of covalent serine β-lactamase inhibitors, the O-aryloxycarbonyl hydroxamates, that inactivated these enzymes by a unique mechanism in which the active site became cross-linked. We describe in this paper some new variants of this class of inhibitor. First, we investigated compounds in which more polar hydroxamates were incorporated. These were generally not more active than the original compounds against representative class A and class C β-lactamases, but one of them, 1-(benzoyl)-O-(phenoxycarbonyl)-3-hydroxyurea, was significantly more stable in solution, thus revealing a useful platform for further design. Second, we describe a series of O-(arylphosphoryl) hydroxamates that are also irreversible inactivators of class A and class C β-lactamases, by phosphorylation of the enzyme, as revealed by mass spectra. These compounds did not, however, cross-link the enzyme active site. A striking feature of their structure-activity profile was that hydroxamate remained the leaving group on enzyme phosphorylation rather than aryloxide, even though the aryloxide was intrinsically the better leaving group, as indicated by pKa values and demonstrated by the products of hydrolysis in free solution. Model building suggested that this phenomenon arises from the relative affinity of the enzyme active site components for the two leaving groups. The results obtained for both groups of inhibitors are important for further optimization of these inhibitors.
β-内酰胺类抗生素的有效性受到细菌产生β-内酰胺酶的能力的极大限制。这些酶催化β-内酰胺的水解,从而失去其抗生素活性。β-内酰胺酶抑制剂的研究从β-内酰胺类抗生素引入临床实践后不久就开始了,并且一直持续到今天。不久前,我们引入了一类新的共价丝氨酸β-内酰胺酶抑制剂,即 O-芳氧基羰基羟肟酸,它们通过独特的机制使这些酶失活,其中活性部位发生交联。本文介绍了该类抑制剂的一些新变体。首先,我们研究了含有更多极性羟肟酸的化合物。这些化合物的活性一般不比原始化合物对代表性的 A 类和 C 类β-内酰胺酶更有效,但其中一种化合物 1-(苯甲酰基)-O-(苯氧基羰基)-3-羟基脲在溶液中更加稳定,因此为进一步设计提供了一个有用的平台。其次,我们描述了一系列 O-(芳基膦酰基)羟肟酸,它们也是 A 类和 C 类β-内酰胺酶的不可逆失活剂,通过酶的磷酸化来实现,如质谱所揭示的。然而,这些化合物并没有使酶的活性部位发生交联。它们的结构-活性关系的一个显著特点是,在酶磷酸化时,羟肟酸仍然是离去基团,而不是芳氧基,尽管芳氧基本身是更好的离去基团,这可以通过 pKa 值来指示,并通过游离溶液中水解的产物来证明。模型构建表明,这种现象源于酶活性部位成分对两个离去基团的相对亲和力。这两组抑制剂的结果对于进一步优化这些抑制剂都非常重要。