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Kaczmarski, J.

Publications and source records attributed to Kaczmarski, J..

2 recordsLinked to original sources

Enthalpy-entropy trade-offs in the evolution of ligand specificity in a superfamily of transcription factors

Proteins operate through ligand and solvent interactions governed by thermodynamics, yet the enthalpy-entropy trade-offs that guide their functional evolution remain poorly understood. The LacI/GalR family (LGF) of transcription factors provides a system for examining how these trade-offs evolve over billions of years but has seldom been studied from a full thermodynamic perspective. While the evolution of ligand specificity has been well-studied, the thermodynamic determinants underlying the changes in specificity is not well understood - especially how proteins alter thermodynamic strategies to optimize affinity. By reconstructing LGF ancestors, we reveal a shift from entropy-driven binding in the most distant ancestor, to enthalpy-driven binding in the most recent ancestor and extant LacI. The most distant ancestor is characterized by the ability to bind its ligand in an open and dynamic conformation, and we propose that entropically-driven binding is driven by the presence of entropic reservoirs. This thermodynamic binding trade-off between the most distant and most recent ancestor is in accordance with the concept of ancient life that existed in a hot Earth environment, where higher temperatures enhanced entropically-driven binding. This suggests that molecular binding mechanisms evolved not just for ligand specificity, but to adapt to environmental pressures such as cooling Earth temperatures where enthalpic binding modes are favored.

biochemistry↗

Avid binding by B cells to the Plasmodium circumsporozoite protein repeat suppresses responses to protective subdominant epitopes

Antibodies targeting the NANP/NVDP repeat domain of the Plasmodium falciparum circumsporozoite protein (CSPRepeat) can confer protection against malaria. However, it has also been suggested that this repeat domain exists as a decoy that distracts the immune system from mounting protective responses targeting other domains of CSP. Here we show that B cell responses to the repeat domain are indeed [~]10 fold higher than responses to the N- and C-terminal regions of CSP after sporozoite immunization. We investigated the role of the number of CSPRepeat-specific naive precursor B cells and high avidity binding by B cells in driving the immunodominance of the CSPRepeat. Using adoptive transfer of germline precursors specific for the CSPRepeat, we found that increasing precursor number did indeed increase the responses to the repeat region, but not to the detriment of responses to other epitopes. To investigate the role of avid binding by B cells to the CSPRepeat in driving immunodominance we generated CSP9: a truncated CSP molecule with just 9 NANP repeats. Compared to near full length CSP molecules, CSP9 induced lower BCR signalling in CSPRepeat-specific cells and induced stronger responses to non-repeat epitopes. Finally, we found mice immunized with CSP9 molecules were strongly protected against mosquito bite challenge. Collectively these data demonstrate that the CSPRepeat does function as an immunodominant decoy and that truncated CSP molecules may be a promising avenue for future malaria vaccines. Significance StatementMalaria kills approximately 420,000 individuals each year(1). Our best vaccine, RTS,S/AS01 is based on the circumsporozoite protein that coasts the surface of the parasite. However, this vaccine is only partially protective. Here we show that responses to a repeat region in the circumsporozoite dominate the immune response. However, immunizing with a circumsporozoite protein with a shortened repeat region induces a more diverse immune response, which could be an avenue to make better malaria vaccines.

immunology↗