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Identification of Bilin binding protein from hebomoia glaucippe

ABSTRACT: Hebomoia glaucippe wings (Linnaeus, 1758) protein extraction with lysis buffer containing urea, thiourea, reducing agent, detergent Two dimensional electrophoresis Spot picking

INSTRUMENT(S): Bruker HCTetdII

ORGANISM(S): Hebomoia Glaucippe (great Orangetip Butterfly)

SUBMITTER: Gert Lubec

LAB HEAD: Gert Lubec

PROVIDER: PRD000623 | Pride | 2012-05-01

REPOSITORIES: Pride

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			Action	DRS
	PRIDE_Exp_Complete_Ac_20970.pride.mgf.gz	Mgf
	PRIDE_Exp_Complete_Ac_20970.pride.mztab.gz	Mztab
	PRIDE_Exp_Complete_Ac_20970.xml.gz	Xml
	PRIDE_Exp_Complete_Ac_20971.pride.mgf.gz	Mgf
	PRIDE_Exp_Complete_Ac_20971.pride.mztab.gz	Mztab

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Project description:The identification of putative biomarkers for predicting abdominal aortic aneurysm (AAA) progression can be achieved through proteomic strategies, particularly with shotgun proteomics. However, the heterogeneity of AAA tissue poses challenges for tissue homogenization and protein extraction, compromising reproducibility, an essential factor for clinical translation. Thus, we aimed to optimize a protocol for AAA tissue homogenization and protein extraction and to develop a standard operating procedure (SOP) to maximize protein yield and foster reproducibility in the field. In this context, several experimental variables were systematically tested in a bead-beating method for tissue homogenisation, including bead size (1.4 mm versus 2.8 mm of diameter), the number of extraction cycles (one up to three), a bead-to-tissue mass ratio at 20, 30, or 40, the lysis buffer-to-tissue ratio (10, 15, or 20 μL/mg), and the lysis buffer composition (RIPA, Urea/thiourea, and HEPES). Optimal conditions for protein extraction were achieved using 1.4 mm zirconium dioxide beads in two homogenization cycles, with a bead-to-tissue mass ratio of 30:1 and a lysis buffer-to-tissue ratio of 20 μL lysis buffer per milligram of tissue, in 2 mL O-ring cryotubes. Depending on the purpose of downstream analysis, recommendations for the use of each lysis buffers were provided based on their specific performance across specific indexes. In this context, HEPES and Urea/Thiourea buffers are recommended for studies prioritizing quantification reproducibility, while RIPA buffer is advised for protein extraction reproducibility. As a proof of concept, the optimized SOP was applied to characterize the AAA tissue proteome and several processes and pathways relevant in AAA pathophysiology were highlighted, including blood coagulation, cellular responses to stress, neutrophil degranulation, wound healing, and pathways of the immune system. Additionally, the enrichment analysis identified ECM remodeling and platelet activation, and degranulation as strongly represented pathways across the functional analysis for each buffer, reinforcing their contribution to aneurysm pathophysiology. Hence, these findings demonstrated that the SOP is well-suited for identifying disease-relevant biomarkers and therapeutic targets.

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Identification of Bilin binding protein from hebomoia glaucippe

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