Cloning and expression of soluble truncated variants of Borrelia OspA, OspB and Vmp7
Patent
·
OSTI ID:870674
- Bellport, NY
- San Antonio, TX
A method is provided herein for preparing soluble recombinant variations of Borrelia lipoproteins such as Borrelia burgdorferi outer surface protein A (OspA) and outer surface protein B (OspB), and B. hermsii variable major protein 7 (Vmp7). The method includes synthesizing a set of oligonucleotide primers, amplifying the template DNA utilizing the PCR, purifying the amplification products, cloning the amplification products into a suitable expression vector, transforming a suitable host utilizing the cloned expression vector, cultivating the transformed host for protein production and subsequently isolating and purifying the resulting protein. Also provided are soluble, recombinant variations of Borrelia burgdorferi outer surface protein A (OspA), outer surface protein B (OspB), and B. hermsii variable major protein 7 (Vmp7). The expression vectors harboring DNA encoding the recombinant variations, pET9-OspA, pET9-OspB and pET9-Vmp7, as well as the E. coli host BL21(DE3)/pLysS transformed with each of these vectors, are also disclosed.
- Research Organization:
- ASSOC UNIVERSITIES INC
- DOE Contract Number:
- AC02-76CH00016
- Assignee:
- Associated Universities, Inc. (Washington, DC)
- Patent Number(s):
- US 5571718
- Application Number:
- 07/941,523
- OSTI ID:
- 870674
- Country of Publication:
- United States
- Language:
- English
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amplification
amplifying
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cloned
cloning
coli
cultivating
de3
disclosed
dna
dna encoding
dna utilizing
encoding
expression
expression vector
expression vectors
harboring
hermsii
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major
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oligonucleotide
oligonucleotide primer
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ospa
ospb
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pet9-ospb
pet9-vmp7
plyss
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purifying
recombinant
resulting
set
soluble
subsequently
suitable
suitable host
surface
synthesizing
template
transformed
transformed host
transforming
truncated
utilizing
variable
variants
variations
vector
vectors
vmp7
amplification
amplifying
bl21
borrelia
burgdorferi
cloned
cloning
coli
cultivating
de3
disclosed
dna
dna encoding
dna utilizing
encoding
expression
expression vector
expression vectors
harboring
hermsii
host
isolating
lipoproteins
major
method
oligonucleotide
oligonucleotide primer
oligonucleotide primers
ospa
ospb
outer
outer surface
pcr
pet9-ospa
pet9-ospb
pet9-vmp7
plyss
preparing
primers
production
products
protein
provided
purifying
recombinant
resulting
set
soluble
subsequently
suitable
suitable host
surface
synthesizing
template
transformed
transformed host
transforming
truncated
utilizing
variable
variants
variations
vector
vectors
vmp7