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ABSTRACT: Gila Monster, Heloderma suspectum, restriction site-associated DNA sequencing data (ddRADseq) throughout Nevada and Utah, USA (2018-2020)

PROVIDER: PRJNA844500 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR19514400.fastq.gz	Fastqsanger.gz
	SRR19514401.fastq.gz	Fastqsanger.gz
	SRR19514402.fastq.gz	Fastqsanger.gz
	SRR19514403.fastq.gz	Fastqsanger.gz
	SRR19514404.fastq.gz	Fastqsanger.gz

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Project description:The archetypical venomous lizard species are the helodermatids, the Gila Monster (Heloderma suspectum) and the Beaded Lizards (Heloderma horridum). In the present study, the gila monster venom proteome was characterized using 2D-gel electrophoresis and tandem mass spectrometry-based de novo peptide sequencing followed by protein identification based on sequence homology. A total of 39 different proteins were identified out of the 58 selected spots that represent the major constituents of venom. Of these proteins, 19 have not previously been identified in helodermatid venom. The data showed that helodermatid venom is complex and that this complexity is caused by genetic isoforms and post-translational modifications including proteolytic processing. In addition, the venom proteome analysis revealed that the major constituents of the gila monster venom are kallikrein-like serine proteinases (EC 3.4.21) and phospholipase A2 (type III) enzymes (EC 3.1.1.4). A neuroendocrine convertase 1 homolog that most likely converts the proforms of the previously identified bioactive exendins into the mature and active forms was identified suggesting that these peptide toxins are secreted as proforms that are activated by proteolytic cleavage following secretion as opposed to being activated intracellularly. The presented global protein identification-analysis provides the first overview of the helodermatid venom composition.

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