Pixton David A, Petersen Christine A, Franke Alicja, van Eldik Rudi, Garton Elizabeth M, Andrew Colin R
Department of Chemistry and Biochemistry, Eastern Oregon University, One University Boulevard, La Grande, Oregon 97850-2899, USA.
J Am Chem Soc. 2009 Apr 8;131(13):4846-53. doi: 10.1021/ja809587q.
The bacterial heme protein Alcaligenes xylosoxidans cytochrome c' (AXCP) forms a novel five-coordinate heme-nitrosyl (5c-NO) complex in which NO resides at the proximal heme face in place of the endogenous protein ligand. Intriguingly, AXCP shares NO-binding properties with the eukaryotic NO-sensor, soluble guanylate cyclase (sGC), including 5c-NO formation via two NO-dependent reactions. For both proteins, a model has been proposed in which NO binds to the vacant distal face to form a transient six-coordinate heme-nitrosyl (6c-NO) species, which then converts to a proximal 5c-NO complex via a putative dinitrosyl intermediate. To shed light on this novel reaction mechanism, activation parameters have been determined for distal and proximal NO-binding reactions in AXCP from the effect of temperature and hydrostatic pressure on rate constants. The unusually slow 6c-NO formation reaction has a near-zero entropy of activation and a positive volume of activation (DeltaV(double dagger) = +14.1 cm(3) mol(-1)), consistent with a rate-determining step involving movement of the Leu 16 residue to allow NO binding to the crowded distal site. For the 6c-NO --> 5c-NO conversion, the large positive entropy of activation (DeltaS(double dagger) = +103 J K(-1) mol(-1)) and volume of activation (DeltaV(double dagger) = +24.1 cm(3) mol(-1)) suggest that the putative dinitrosyl intermediate forms via a dissociative mechanism in which the endogenous His ligand dissociates prior to the attack of the second NO molecule on the proximal heme face. These results have important implications for distal vs proximal NO binding in AXCP, as well as mechanisms of 5c-NO formation in heme proteins.
细菌血红素蛋白木糖氧化产碱杆菌细胞色素c'(AXCP)形成一种新型的五配位血红素-亚硝酰基(5c-NO)复合物,其中NO取代内源性蛋白质配体位于血红素近端表面。有趣的是,AXCP与真核生物的NO传感器可溶性鸟苷酸环化酶(sGC)具有相同的NO结合特性,包括通过两个NO依赖性反应形成5c-NO。对于这两种蛋白质,都提出了一个模型,其中NO与空的远端表面结合形成瞬态六配位血红素-亚硝酰基(6c-NO)物种,然后通过假定的二亚硝酰基中间体转化为近端5c-NO复合物。为了阐明这种新的反应机制,通过温度和静水压力对速率常数的影响,确定了AXCP中远端和近端NO结合反应的活化参数。异常缓慢的6c-NO形成反应具有接近零的活化熵和正的活化体积(ΔV‡ = +14.1 cm³ mol⁻¹),这与涉及Leu 16残基移动以使NO结合到拥挤的远端位点的速率决定步骤一致。对于6c-NO→5c-NO的转化,较大的正活化熵(ΔS‡ = +103 J K⁻¹ mol⁻¹)和活化体积(ΔV‡ = +24.1 cm³ mol⁻¹)表明假定的二亚硝酰基中间体通过解离机制形成,其中内源性His配体在第二个NO分子攻击近端血红素表面之前解离。这些结果对于AXCP中远端与近端NO结合以及血红素蛋白中5c-NO形成的机制具有重要意义。