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Identification, Baculoviral Expression, and Biochemical Characterization of a Novel Cholinesterase of Amblyomma americanum (Acari: Ixodidae)

dc.contributor.authorTemeyer, Kevin B.en
dc.contributor.authorSchlechte, Kristie G.en
dc.contributor.authorGross, Aaron D.en
dc.contributor.authorLohmeyer, Kimberly H.en
dc.date.accessioned2023-04-27T14:53:22Zen
dc.date.available2023-04-27T14:53:22Zen
dc.date.issued2023-04-22en
dc.date.updated2023-04-27T13:50:47Zen
dc.description.abstractA cDNA encoding a novel cholinesterase (ChE, EC 3.1.1.8) from the larvae of <i>Amblyomma americanum</i> (Linnaeus) was identified, sequenced, and expressed in <i>Sf21</i> insect cell culture using the baculoviral expression vector pBlueBac4.5/V5-His. The open reading frame (1746 nucleotides) of the cDNA encoded 581 amino acids beginning with the initiation codon. Identical cDNA sequences were amplified from the total RNA of adult tick synganglion and salivary gland, strongly suggesting expression in both tick synganglion and saliva. The recombinant enzyme (rAaChE1) was highly sensitive to eserine and BW284c51, relatively insensitive to tetraisopropyl pyrophosphoramide (iso-OMPA) and ethopropazine, and hydrolyzed butyrylthiocholine (BuTCh) 5.7 times as fast as acetylthiocholine (ATCh) at 120 &micro;M, with calculated <i>K</i><sub>M</sub> values for acetylthiocholine (ATCh) and butyrylthiocholine of 6.39 &micro;M and 14.18 &micro;M, respectively. The recombinant enzyme was highly sensitive to inhibition by malaoxon, paraoxon, and coroxon in either substrate. Western blots using polyclonal rabbit antibody produced by immunization with a peptide specific for rAaChE1 exhibited reactivity in salivary and synganglial extract blots, indicating the presence of AaChE1 antigenic protein. Total cholinesterase activities of synganglial or salivary gland extracts from adult ticks exhibited biochemical properties very different from the expressed rAaACh1 enzyme, evidencing the substantial presence of additional cholinesterase activities in tick synganglion and saliva. The biological function of AaChE1 remains to be elucidated, but its presence in tick saliva is suggestive of functions in hydrolysis of cholinergic substrates present in the large blood mean and potential involvement in the modulation of host immune responses to tick feeding and introduced pathogens.en
dc.description.versionPublished versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationTemeyer, K.B.; Schlechte, K.G.; Gross, A.D.; Lohmeyer, K.H. Identification, Baculoviral Expression, and Biochemical Characterization of a Novel Cholinesterase of Amblyomma americanum (Acari: Ixodidae). Int. J. Mol. Sci. 2023, 24, 7681.en
dc.identifier.doihttps://doi.org/10.3390/ijms24097681en
dc.identifier.urihttp://hdl.handle.net/10919/114824en
dc.language.isoenen
dc.publisherMDPIen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subjectsalivary cholinesteraseen
dc.subjectsynganglionen
dc.subjectixodid ticken
dc.subjectlone star ticken
dc.subjectvector-borne diseaseen
dc.titleIdentification, Baculoviral Expression, and Biochemical Characterization of a Novel Cholinesterase of Amblyomma americanum (Acari: Ixodidae)en
dc.title.serialInternational Journal of Molecular Scienceen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten

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