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Regulation of Protein Nitrosylation by Thioredoxin 1

  • Narayani Nagarajan
  • Junichi SadoshimaEmail author
Chapter
Part of the Advances in Biochemistry in Health and Disease book series (ABHD, volume 16)

Abstract

Addition of an SNO group to a cysteine thiol in a protein is called protein S-nitrosylation. When the donor of the SNO group is another protein, then the transfer is referred to as trans-nitrosylation. One key protein that mediates trans-nitrosylation and denitrosylation is thioredoxin1 (Trx1). Trx1 is a 12 kDa redox protein with five cysteine residues: Cys32, 35, 62, 69 and 73. Factors such as pH conditions and cysteine residue redox status affect the S-nitrosylation of Trx1. Several studies have reported that Trx1 promotes trans-nitrosylation of caspase-3, ASK1, and peroxiredoxin-1. On the other hand, Trx1 can trigger denitrosylation of SNO-caspase-3, SNO-metallothionein, SNO-albumin, SNO-caspase-8, GAPDH, annexin-1, etc. By regulating the balance between S-nitrosylation and denitrosylation, Trx1 helps maintain the nitroso-redox balance in the cell. Trx1-mediated S-nitrosylation and denitrosylation of proteins affect several cellular functions, including apoptosis, heme protein maturation and insertion, and exocytosis as well as various pathophysiological conditions, such as inflammation, cancer and cardiovascular diseases. In this chapter, we shall discuss in detail the molecular mechanism of Trx1-mediated trans-nitrosylation and denitrosylation and its importance in the cellular milieu.

Keywords

Thioredoxin 1 Protein S-nitrosylation Denitrosylation Trans-nitrosylation Cardiovascular diseases Cancer Inflammation 

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Copyright information

© Springer International Publishing Switzerland 2016

Authors and Affiliations

  1. 1.Department of Cell Biology and Molecular Medicine, Cardiovascular Research InstituteRutgers New Jersey Medical SchoolNewarkUSA

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