Literature DB >> 33074537

Identification of SH2 Domain-Mediated Protein Interactions that Operate at Fertilization in the Sea Star Patiria miniata.

Lauren Bates1, Emily Wiseman2, Jamie Kitson2, David J Carroll3.   

Abstract

The signaling mechanisms controlling internal calcium release at fertilization in animals are still largely unknown. Echinoderms, such as the sea star Patiria miniata, produce abundant and easily accessible sperm and eggs. In addition, eggs are naturally synchronized at the same cell cycle stage, collectively making these animals an attractive model to study the signaling proteins controlling fertilization. However, the lack of antibodies to identify proteins in this model system has slowed progress in identifying key signaling molecules. With the advances in mass spectrometry, we present a method for identifying tyrosine phosphorylated proteins binding to GST-tagged SH2 domains in sea star cell lysates for downstream mass spectrometry analysis.

Entities:  

Keywords:  Affinity interaction; Ca release; Egg activation; Fertilization; GST fusion protein; Phospholipase C gamma; Src Family Kinase

Mesh:

Year:  2021        PMID: 33074537     DOI: 10.1007/978-1-0716-0974-3_7

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  The amino-terminal Src homology 2 domain of phospholipase C gamma 1 is essential for TCR-induced tyrosine phosphorylation of phospholipase C gamma 1.

Authors:  B Stoica; K E DeBell; L Graham; B L Rellahan; M A Alava; J Laborda; E Bonvini
Journal:  J Immunol       Date:  1998-02-01       Impact factor: 5.422

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.