Functional analysis of primers and templates in the synthesis of DNA catalyzed by human immunodeficiency virus type 1 reverse transcriptase

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Abstract
The kinetics of copying of poly(A) · (dT)n, poly(A) · (U)n, poly(dA) · (dT)n and poly(A) · (dT)9‐U by reverse transcriptase of human immunodeficiency virus‐1 (HIV‐1) has been studied and the binding affinity of the enzyme, for template or primer, determined. Short oligonucleotides and dTTP served as primers in the HIV‐1 reverse‐transcriptase‐dependent DNA synthesis. Km and Vmax were measured as functions of the primer chain length; the logarithm of the values of both Km and Vmax increased linearly up to 10. For longer primers (n= 11 to n= 24) the increase of those values changes very little. The enhanced affinity of the primers, (dT)n or (U)n due to the formation of one complementary pair, A · dT, dA · dT, A · U was estimated as a factor of 2. A specific property of HIV‐1 reverse transcriptase compared with other DNA polymerases (procaryotes, eucaryotes, other retroviruses and archaebacteria) was its higher affinity to riboprimers as compared to deoxyriboprimers. Relative initial rates when copying poly(A) or poly(dA) templates using different primers and various conditions were compared; the optimal temperature for the reaction of polymerization with poly(A) or poly(dA) templates and (U)10, (dT)10 or (dT)9‐U primers was determined. The maximal activity of the enzyme in the case of poly(A) and decanucleotide primers was found at temperatures between 27–31°C. An increase in the primer length results in the stabilization of the template · primer duplex complexed to the enzyme, thus increasing to more than 40°C the optimal temperature of polymerization. The activation energy (Ea) values of the polymerization reaction for different template · primer complexes were evaluated.

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