KOPS - Das Institutionelle Repositorium der Universität Konstanz

Exploring the Effects of Active Site Constraints on HIV-1 Reverse Transcriptase DNA Polymerase Fidelity

Exploring the Effects of Active Site Constraints on HIV-1 Reverse Transcriptase DNA Polymerase Fidelity

Zitieren

Dateien zu dieser Ressource

Prüfsumme: MD5:1fcf23768224f876484cbb0da0144a47

CRAMER, Janina, Michael STRERATH, Andreas MARX, Tobias RESTLE, 2002. Exploring the Effects of Active Site Constraints on HIV-1 Reverse Transcriptase DNA Polymerase Fidelity. In: Journal of Biological Chemistry : JBC. 277(46), pp. 43593-43598. ISSN 0021-9258. eISSN 1083-351X. Available under: doi: 10.1074/jbc.M207854200

@article{Cramer2002-11-15Explo-33842, title={Exploring the Effects of Active Site Constraints on HIV-1 Reverse Transcriptase DNA Polymerase Fidelity}, year={2002}, doi={10.1074/jbc.M207854200}, number={46}, volume={277}, issn={0021-9258}, journal={Journal of Biological Chemistry : JBC}, pages={43593--43598}, author={Cramer, Janina and Strerath, Michael and Marx, Andreas and Restle, Tobias} }

2002-11-15 Cramer, Janina Cramer, Janina Exploring the Effects of Active Site Constraints on HIV-1 Reverse Transcriptase DNA Polymerase Fidelity Restle, Tobias Strerath, Michael 2016-05-09T13:52:01Z Restle, Tobias To examine the concept of polymerase active site tightness as a criteria for DNA polymerase fidelity, we performed pre-steady-state single nucleotide incorporation kinetic analyses with sugar modified thymidine 5'-triphosphate (TTP) analogues and human immunodeficiency virus (HIV-1) reverse transcriptase (RT). The employed TTP analogues (T<sup>R</sup>TP) are modified at the 4'-position of the sugar moiety with alkyl groups, gradually expanding their steric demand. Introduction of a methyl group reduces the maximum rate of nucleotide incorporation by about 200-fold for RT<sup>WT</sup> and about 400-fold for RT<sup>M184V</sup>. Interestingly, the affinity of RT for the modified nucleotide is only marginally affected. Increasing the size to an ethyl group leads to further reduction of the rate of incorporation and first effects on binding affinities are observed. Finally, substitution for an isopropyl group results not only in a further reduction of incorporation rates but also in a dramatic loss of binding affinity for the nucleotide analogue. By increasing the steric demand the effects on RT<sup>M184V</sup> in comparison with RT<sup>WT</sup> become progressively more pronounced. Misincorporation of either TTP or T<sup>Me</sup>TP opposite a template G causes additional decline in incorporation rates accompanied by a drastic decrease in binding affinities. This results in relative incorporation efficiencies [(k(pol)/K(d))(incorrect)/(k(pol)/K(d))(TTPcorrect)] of 4.1 x 10<sup>-5</sup> for TTP and 3.4 x 10<sup>-6</sup> for T<sup>Me</sup>TP in case of RT<sup>WT</sup> and 1.4 x 10<sup>-5</sup> for TTP and 2.9 x 10<sup>-8</sup> for T<sup>Me</sup>TP in case of RT<sup>M184V</sup>. 2016-05-09T13:52:01Z Marx, Andreas eng Strerath, Michael Marx, Andreas

Dateiabrufe seit 09.05.2016 (Informationen über die Zugriffsstatistik)

Cramer_0-329661.pdf 171

Das Dokument erscheint in:

KOPS Suche


Stöbern

Mein Benutzerkonto