Protein S-nitrosylation:: Purview and parameters

被引：1687

作者：

Hess, DT

Matsumoto, A

Kim, SO

Marshall, HE

Stamler, JS

机构：

[1] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA

[2] Duke Univ, Med Ctr, Dept Biochem, Durham, NC 27710 USA

[3] Duke Univ, Med Ctr, Howard Hughes Med Inst, Durham, NC 27710 USA

来源：

NATURE REVIEWS MOLECULAR CELL BIOLOGY | 2005年 / 6卷 / 02期

关键词：

D O I：

10.1038/nrm1569

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

S-nitrosylation, the covalent attachment of a nitrogen monoxide group to the thiol side chain of cysteine, has emerged as an important mechanism for dynamic, post-translational regulation of most or all main classes of protein. S-nitrosylation thereby conveys a large part of the ubiquitous influence of nitric oxide (NO) on cellular signal transduction, and provides a mechanism for redox-based physiological regulation.

引用

收藏

页码：150 / 166

页数：17

相关论文

共 154 条

[1] Nitric oxide controls Src kinase activity through a sulfhydryl group modification-mediated Tyr-527-independent and Tyr-416-linked mechanism [J].

Akhand, AK ;

Pu, MY ;

Senga, T ;

Kato, M ;

Suzuki, H ;

Miyata, T ;

Hamaguchi, M ;

Nakashima, I .

JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (36) :25821-25826

[2] Interactive effects of nitric oxide and the p53 tumor suppressor gene in carcinogenesis and tumor progression [J].

Ambs, S ;

Hussain, SP ;

Harris, CC .

FASEB JOURNAL, 1997, 11 (06) :443-448

[3] S-glutathionylation decreases Mg2+ inhibition and S-nitrosylation enhances Ca2+ activation of RyR1 channels [J].

Aracena, P ;

Sánchez, G ;

Donoso, P ;

Hamilton, SL ;

Hidalgo, C .

JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (44) :42927-42935

[4] NO+, NO(CENTER-DOT), AND NO- DONATION BY S-NITROSOTHIOLS - IMPLICATIONS FOR REGULATION OF PHYSIOLOGICAL FUNCTIONS BY S-NITROSYLATION AND ACCELERATION OF DISULFIDE FORMATION [J].

ARNELLE, DR ;

STAMLER, JS .

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 318 (02) :279-285

[5]

ATKINS WM, 1993, J BIOL CHEM, V268, P19188

[6] Nitric oxide regulates the heart by spatial confinement of nitric oxide synthase isoforms [J].

Barouch, LA ;

Harrison, RW ;

Skaf, MW ;

Rosas, GO ;

Cappola, TP ;

Kobeissi, ZA ;

Hobai, IA ;

Lemmon, CA ;

Burnett, AL ;

O'Rourke, B ;

Rodriguez, ER ;

Huang, PL ;

Lima, JAC ;

Berkowitz, DE ;

Hare, JM .

NATURE, 2002, 416 (6878) :337-340

[7] S-N dissociation energies of S-nitrosothiols:: On the origins of nitrosothiol decomposition rates [J].

Bartberger, MD ;

Mannion, JD ;

Powell, SC ;

Stamler, JS ;

Houk, KN ;

Toone, EJ .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (36) :8868-8869

[8] Theory, spectroscopy, and crystallographic analysis of S-nitrosothiols:: Conformational distribution dictates spectroscopic behavior [J].

Bartberger, MD ;

Houk, KN ;

Powell, SC ;

Mannion, JD ;

Lo, KY ;

Stamler, JS ;

Toone, EJ .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (24) :5889-5890

[9] Nitric oxide inhibits ornithine decarboxylase via S-nitrosylation of cysteine 360 in the active site of the enzyme [J].

Bauer, PM ;

Buga, GM ;

Fukuto, JM ;

Pegg, AE ;

Ignarro, LJ .

JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (37) :34458-34464

[10] Structural determinants influencing the reaction of cysteine-containing peptides with palmitoyl-coenzyme A and other thioesters [J].

Bizzozero, OA ;

Bixler, HA ;

Pastuszyn, A .

BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2001, 1545 (1-2) :278-288

← 1 2 3 4 5 6 7 8 9 10 →