Expression and Purification of Snake Antivenom Peptide in Pichia pastoris

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" Expression and Purification of Snake Antivenom Peptide in Pichia pastoris "
Juarez Contreras, Israel Komives, Claire

Document Type	:	Latin Dissertation
Language of Document	:	English
Record Number	:	1106268
Doc. No	:	TLpq2383389006
Main Entry	:	Juarez Contreras, Israel
	:	Komives, Claire
Title & Author	:	Expression and Purification of Snake Antivenom Peptide in Pichia pastoris\ Juarez Contreras, IsraelKomives, Claire
College	:	San Jose State University
Date	:	2019
student score	:	2019
Degree	:	M.S.
Page No	:	54
Abstract	:	It has been shown that a peptide of the first 10-15 N-terminal amino acids of the lethal toxin neutralizing factor (LTNF) protein found in opossums (Didelphis spp.) holds promise as a low-cost therapy for snake envenomation. To date, the 11-mer has been expressed in E. coli and shown to neutralize snake venoms. However, possible endotoxin concerns warrant an investigation into other microbial hosts. The methylotrophic yeast, Pichia pastoris, shows promise as an alternative host. Active LTNF peptide was expressed and purified in P. pastoris. This was accomplished by subcloning a tandem repeat of the first 15 N-terminal amino acids of lethal toxin neutralizing factor (LTNF-15) into the Pichia expression vector, PPIC9K and transforming the yeast via electroporation. Expression of LTNF-15 from Pichia was verified by applying a fluorescent histidine tag stain onto a SDS-PAGE gel containing supernatant samples of P. pastoris clones. Purification of the LTNF-15 peptide was conducted by Ni-NTA purification. It was found that expressed LTNF-15 peptide demonstrated neutralizing activity in an in vitro assay using azocasein. In addition, it was determined that a protein concentration of 70 mg/L of LTNF-15 was attained during the fermentation process. Thus, showing promise of Pichia as a viable production host.
Subject	:	Biochemistry
	:	Bioengineering
	:	Chemical engineering