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Expression, purification, crystallization and crystallographic study of Lutzomyia longipalpis LJL143.

Authors :
Kelleher A
Liu Z
Seid CA
Zhan B
Asojo OA
Source :
Acta crystallographica. Section F, Structural biology communications [Acta Crystallogr F Struct Biol Commun] 2015 Jul; Vol. 71 (Pt 7), pp. 925-8. Date of Electronic Publication: 2015 Jun 27.
Publication Year :
2015

Abstract

Leishmaniasis is a neglected vector-borne disease with a global prevalence of over 12 million cases and 59,000 annual deaths. Transmission of the parasite requires salivary proteins, including LJL143 from the New World sandfly Lutzomyia longipalpis. LJL143 is a known marker of sandfly exposure in zoonotic hosts. LJL143 was crystallized from soluble protein expressed using Pichia pastoris. X-ray data were collected to 2.6 Å resolution from orthorhombic crystals belonging to space group P2(1)2(1)2(1), with average unit-cell parameters a = 57.39, b = 70.24, c = 79.58 Å. The crystals are predicted to have a monomer in the asymmetric unit, with an estimated solvent content of 48.5%. LJL143 has negligible homology to any reported structures, so the phases could not be determined by molecular replacement. All attempts at S-SAD failed and future studies include experimental phase determination using heavy-atom derivatives.

Details

Language :
English
ISSN :
2053-230X
Volume :
71
Issue :
Pt 7
Database :
MEDLINE
Journal :
Acta crystallographica. Section F, Structural biology communications
Publication Type :
Academic Journal
Accession number :
26144240
Full Text :
https://doi.org/10.1107/S2053230X15009486