Walker F Ann
Department of Chemistry, University of Arizona, PO 210041, Tucson, AZ 85721-0041, USA.
J Inorg Biochem. 2005 Jan;99(1):216-36. doi: 10.1016/j.jinorgbio.2004.10.009.
The nitrophorins are NO-carrying heme proteins that are found in the saliva of two species of blood-sucking insects, the kissing bug (Rhodnius prolixus) and the bedbug (Cimex lectularius). In both insects the NO is bound to the ferric form of the protein, which gives rise to Kds in the micromolar to nanomolar range, and thus upon injection of the saliva into the tissues of the victim the NO can dissociate to cause vasodilation and inhibition of platelet aggregation. The structures of the proteins from each of these insects are unique, and each has a large component of beta-sheet structure, which is unusual for heme proteins. While the Rhodnius nitrophorins increase the effectiveness of their NO-heme proteins by also binding histamine, secreted by the victim in response to the bite, to the heme, the Cimex nitrophorin does not bind histamine but rather binds two molecules of NO reversibly, one to the heme and the other to the cysteine thiolate which serves as the heme ligand in the absence of NO. This requires homolytic cleavage of the Fe-S-Cys bond, which produces an EPR-active Fe(II)-NO complex having the {FeNO}7 electron configuration. For the Rhodnius nitrophorins, the heme of the {FeNO}6 stable NO complex could have the limiting electron configurations Fe(III)-NO+ or Fe(II)-NO+. While vibrational spectroscopy suggests the latter and Mossbauer spectroscopy cannot differentiate between a purely diamagnetic Fe(II) center and a strongly antiferromagnetically coupled Fe(III)-NO* center, the strong ruffling of the heme (with alternate meso-carbons shifted significantly above and below the mean plane of the porphyrin, and concomitant shifts of the beta-pyrrole carbons above and below the mean plane of the porphyrin ring, to produce a very nonplanar porphyrin macrocycle) may suggest at least an important contribution of the latter. The strong ruffling would help to stabilize the (dxz, dyz)4(dxy)1 electron configuration of low-spin Fe(III) (but not low-spin Fe(II)), and the dxy orbital does not have correct symmetry for overlap with the half-filled pi* orbital of NO. This Fe(III)-NO* electron configuration would facilitate reversible dissociation of NO.
嗜硝酸盐蛋白是一类携带一氧化氮(NO)的血红素蛋白,存在于两种吸血昆虫的唾液中,即锥蝽(红带锥蝽)和臭虫(温带臭虫)。在这两种昆虫中,NO与蛋白的三价铁形式结合,其解离常数在微摩尔到纳摩尔范围内,因此当唾液注入受害者组织时,NO会解离,导致血管舒张并抑制血小板聚集。这两种昆虫的嗜硝酸盐蛋白结构独特,且都有很大一部分β-折叠结构,这对血红素蛋白来说并不常见。红带锥蝽的嗜硝酸盐蛋白通过将受害者被咬后分泌的组胺也结合到血红素上,提高了其NO-血红素蛋白的有效性,而温带臭虫的嗜硝酸盐蛋白不结合组胺,而是可逆地结合两个NO分子,一个结合到血红素上,另一个结合到在没有NO时作为血红素配体的半胱氨酸硫醇盐上。这需要Fe-S-Cys键的均裂,产生具有{FeNO}7电子构型的EPR活性Fe(II)-NO络合物。对于红带锥蝽的嗜硝酸盐蛋白,{FeNO}6稳定NO络合物的血红素可能具有极限电子构型Fe(III)-NO+或Fe(II)-NO+。虽然振动光谱表明是后者,且穆斯堡尔光谱无法区分纯抗磁性的Fe(II)中心和强反铁磁耦合的Fe(III)-NO中心,但血红素的强烈褶皱(卟啉的交替中位碳显著高于和低于卟啉平均平面,且β-吡咯碳伴随性地高于和低于卟啉环平均平面,以产生非常非平面的卟啉大环)可能至少表明后者有重要贡献。强烈的褶皱有助于稳定低自旋Fe(III)(而非低自旋Fe(II))的(dxz, dyz)4(dxy)1电子构型,且dxy轨道与NO的半填充π轨道重叠时没有正确的对称性。这种Fe(III)-NO*电子构型将促进NO的可逆解离。