Nitrophorins - Lipocalin-based heme proteins transporting nitric oxide

被引:13
作者
Ascenzi, P
Nardini, M
Bolognesi, M
Montfort, WR
机构
[1] Univ Rome Tre, Dept Biol, I-00146 Rome, Italy
[2] Univ Genoa, Adv Biotechnol Ctr, I-16132 Genoa, Italy
[3] Univ Genoa, Dept Phys, Natl Inst Phys Matter, I-16132 Genoa, Italy
[4] Univ Arizona, Dept Biochem & Mol Biophys, Tucson, AZ 85721 USA
关键词
heme protein; hemoglobin; lipocalin; nitrophorin; nitric oxide storage; nitric oxide transport; histamine sequestering; anticoagulation activity;
D O I
10.1002/bmb.2002.494030010016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Nitrophorins 1-4 (NPs; NP1 to NP4) are salivary heme proteins secreted from the blood-sucking insect Rhodnius prolixus. NPs transfer nitric oxide (NO) to the victim, resulting in vasodilatation, sequester histamine, reducing host inflammation and immune response, and inhibit blood coagulation. The NP fold is based on an eight-stranded antiparallel beta-barrel, typically observed in the lipocalin homology family, which hosts a heme group. Although NPs use the ferric heme to bind NO and histamine, they are unrelated to the six/eight alpha-helix (non)vertebrate hemoglobins, which bind NO preferentially to the ferrous heme, but do not bind histamine. Therefore, NPs and hemoglobins can be considered as an evolutionary experiment, where the heme group has been adapted to structurally different protein families to achieve similar function(s).
引用
收藏
页码:68 / 71
页数:4
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