HIV infection continues to pose a significant global health challenge,with subSaharan Africa bearing a disproportionate burden.The replication cycle of HIV is fundamentally driven by intricate molecular interactions.T...HIV infection continues to pose a significant global health challenge,with subSaharan Africa bearing a disproportionate burden.The replication cycle of HIV is fundamentally driven by intricate molecular interactions.This study investigates the competitive biochemical interplay between reverse transcriptase(RT)and integrase(IN)enzymes,employing a fractional calculus framework to model their mutual inhibitory effects.Through the application of fixed-point theory and Picard stability analysis,the existence,uniqueness,and stability of the fractional-order system are rigorously established.The role of RT-IN enzymatic competition in influencing HIV replication dynamics is elucidated through global sensitivity analysis using Latin Hypercube Sampling.Furthermore,the model incorporates memory-dependent characteristics by examining three distinct fractional operators,namely,the Caputo,Caputo-Fabrizio,and Atangana-Baleanu operators in the Caputo sense,thereby elucidating their respective influences on system behavior.The Atangana-Baleanu operator,in particular,demonstrates an enhanced capacity to capture the complex,synergistic processes underpinning HIV progression.This research provides a critical nexus between molecular virology and applied mathematics,offering foundational insights for the advancement of more precise and targeted therapeutic strategies against HIV.展开更多
基金Supported by the DST FIST Programme(SR/FST/MS-II/2021/101(C))UGC-JRF(21161010788)+1 种基金supported by NSFC(11831003,12171111)SFC(KZ202110005011)。
文摘HIV infection continues to pose a significant global health challenge,with subSaharan Africa bearing a disproportionate burden.The replication cycle of HIV is fundamentally driven by intricate molecular interactions.This study investigates the competitive biochemical interplay between reverse transcriptase(RT)and integrase(IN)enzymes,employing a fractional calculus framework to model their mutual inhibitory effects.Through the application of fixed-point theory and Picard stability analysis,the existence,uniqueness,and stability of the fractional-order system are rigorously established.The role of RT-IN enzymatic competition in influencing HIV replication dynamics is elucidated through global sensitivity analysis using Latin Hypercube Sampling.Furthermore,the model incorporates memory-dependent characteristics by examining three distinct fractional operators,namely,the Caputo,Caputo-Fabrizio,and Atangana-Baleanu operators in the Caputo sense,thereby elucidating their respective influences on system behavior.The Atangana-Baleanu operator,in particular,demonstrates an enhanced capacity to capture the complex,synergistic processes underpinning HIV progression.This research provides a critical nexus between molecular virology and applied mathematics,offering foundational insights for the advancement of more precise and targeted therapeutic strategies against HIV.
