Journal of biomedical science · 2026
Calcium and phosphorylation coordination is a novel mechanism that stabilises protein-complexes during HIV assembly.
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Brémaud Erwan, Mishra Biswa Prasanna, Baqi Ablikim, Masic Veronika, Flipo Thibaut, Everest-Dass Arun, Hartley-Tassell Lauren, Gorry Paul R, Ve Thomas, Spillings Belinda L, Mak Johnson
Аннотация
BACKGROUND: Calcium (Ca2+) signalling and phosphorylation are independent mechanisms that regulate diverse biological processes. It is, however, not appreciated that a normal function of phospho-mimic amino acids (aspartate/glutamate) is to interact with Ca2+ at the atomic level.
METHODS: In this work, we have utilised a combination of molecular virology, phosphorylation proteomics mass spectrometry, surface plasmon resonance, nuclear magnetic resonance, AlphaFold structural prediction, and electron microscopy imaging to systematically evaluated the biology of calcium - phosphorylation interplay.
RESULTS: Here, we leveraged HIV-Ca2+ biology to enable polarised targeting in primary cells to describe an unknown layer of regulatory processes via Ca2+-phosphate (PO43-) bridge to support protein complex formation. We identified novel HIV phosphorylation sites proximal to Endosomal Sorting Complex Required for Transport (ESCRT) binding motifs and potential Ca2+ binding sites through phospho-proteomics. Integrating primary cells, molecular virology, structural biology, biophysical and ultrastructural analyses, we presented multiple examples of coordination between calcium and phosphorylated amino acids to support HIV assembly and function. Our data suggest Ca2+-PO43- could form a bridge between intrinsically disordered protein regions of HIV to: (i) stabilise Pr55Gag-Pr160GagPol complex for virus function; (ii) mediate p6Pol dimerization to support virion maturation; and (iii) modulate viral complex formation to package both viral enzymatic- and cellular- proteins.
CONCLUSIONS: Our work has identified the coordination between calcium and phosphorylated amino acids (presumably via the formation of a salt-bridge) is an unknown layer of regulation that support protein complex formation. In the context of HIV, these Ca2+-PO43- cooperation via the intrinsically disordered protein regions regulates the assembly of HIV complex and modulates its interactions with ESCRT cellular proteins. Importantly, the convergent enrichment of calcium-phosphorylation domains across a wide range of viral and cellular intrinsically disordered protein regions implies Ca2+-PO43- cooperation to be a general regulatory principle in biology.
METHODS: In this work, we have utilised a combination of molecular virology, phosphorylation proteomics mass spectrometry, surface plasmon resonance, nuclear magnetic resonance, AlphaFold structural prediction, and electron microscopy imaging to systematically evaluated the biology of calcium - phosphorylation interplay.
RESULTS: Here, we leveraged HIV-Ca2+ biology to enable polarised targeting in primary cells to describe an unknown layer of regulatory processes via Ca2+-phosphate (PO43-) bridge to support protein complex formation. We identified novel HIV phosphorylation sites proximal to Endosomal Sorting Complex Required for Transport (ESCRT) binding motifs and potential Ca2+ binding sites through phospho-proteomics. Integrating primary cells, molecular virology, structural biology, biophysical and ultrastructural analyses, we presented multiple examples of coordination between calcium and phosphorylated amino acids to support HIV assembly and function. Our data suggest Ca2+-PO43- could form a bridge between intrinsically disordered protein regions of HIV to: (i) stabilise Pr55Gag-Pr160GagPol complex for virus function; (ii) mediate p6Pol dimerization to support virion maturation; and (iii) modulate viral complex formation to package both viral enzymatic- and cellular- proteins.
CONCLUSIONS: Our work has identified the coordination between calcium and phosphorylated amino acids (presumably via the formation of a salt-bridge) is an unknown layer of regulation that support protein complex formation. In the context of HIV, these Ca2+-PO43- cooperation via the intrinsically disordered protein regions regulates the assembly of HIV complex and modulates its interactions with ESCRT cellular proteins. Importantly, the convergent enrichment of calcium-phosphorylation domains across a wide range of viral and cellular intrinsically disordered protein regions implies Ca2+-PO43- cooperation to be a general regulatory principle in biology.