Summary
Sperm are highly specialised cells whose structure is optimised for a defined function. Although the distinctive sperm ultrastructure has been known for many years thanks to electron microscopy, an understanding of the molecular details of sperm specialisation is severely lagging. The gap in our molecular understanding relates to the difficulties in genetically manipulating sperm.
Over the past five years, my lab has pioneered the use of cryo-electron tomography to study mature mammalian sperm at the molecular level. We developed workflows based on cryo-focused ion beam milling and sub-tomogram averaging that allowed us to provide the first in-cell structures of mammalian sperm flagella, revealing unique microtubule inner proteins. We further showed that the sperm centrioles and their surrounding matrix form a dynamic basal complex that facilitates a cascade of internal sliding, coupling tail beating with asymmetric head kinking. Although these findings contribute profoundly to the field, the resolution achieved in these studies (~20Å) precluded protein identification in most cases.
Now I plan to develop a workflow based on single particle analysis, achieving near-atomic resolution, but without purification. I will apply this workflow, together with biochemical assays and cellular cryo-electron tomography, to humans and other species to resolve how germ cells get into shape and acquire motility. Specifically, the mechanisms underlining 1) nuclear shaping 2) centriole remodelling 3) mitochondrial sheath assembly 4) motor apparatus activation.
Understanding how male germ cells get into shape is of clinical relevance, as sperm morphological defects are often observed in infertility. Moreover, the success rate of assisted reproduction technologies can be improved with better diagnosis and we expect that the new proteins we identify will help this process. Conversely, understanding the acquisition of motility could potentially be used to develop a male contraceptive.
Over the past five years, my lab has pioneered the use of cryo-electron tomography to study mature mammalian sperm at the molecular level. We developed workflows based on cryo-focused ion beam milling and sub-tomogram averaging that allowed us to provide the first in-cell structures of mammalian sperm flagella, revealing unique microtubule inner proteins. We further showed that the sperm centrioles and their surrounding matrix form a dynamic basal complex that facilitates a cascade of internal sliding, coupling tail beating with asymmetric head kinking. Although these findings contribute profoundly to the field, the resolution achieved in these studies (~20Å) precluded protein identification in most cases.
Now I plan to develop a workflow based on single particle analysis, achieving near-atomic resolution, but without purification. I will apply this workflow, together with biochemical assays and cellular cryo-electron tomography, to humans and other species to resolve how germ cells get into shape and acquire motility. Specifically, the mechanisms underlining 1) nuclear shaping 2) centriole remodelling 3) mitochondrial sheath assembly 4) motor apparatus activation.
Understanding how male germ cells get into shape is of clinical relevance, as sperm morphological defects are often observed in infertility. Moreover, the success rate of assisted reproduction technologies can be improved with better diagnosis and we expect that the new proteins we identify will help this process. Conversely, understanding the acquisition of motility could potentially be used to develop a male contraceptive.
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| Web resources: | https://cordis.europa.eu/project/id/101088673 |
| Start date: | 01-10-2023 |
| End date: | 30-09-2028 |
| Total budget - Public funding: | 1 999 963,00 Euro - 1 999 963,00 Euro |
Cordis data
Original description
Sperm are highly specialised cells whose structure is optimised for a defined function. Although the distinctive sperm ultrastructure has been known for many years thanks to electron microscopy, an understanding of the molecular details of sperm specialisation is severely lagging. The gap in our molecular understanding relates to the difficulties in genetically manipulating sperm.Over the past five years, my lab has pioneered the use of cryo-electron tomography to study mature mammalian sperm at the molecular level. We developed workflows based on cryo-focused ion beam milling and sub-tomogram averaging that allowed us to provide the first in-cell structures of mammalian sperm flagella, revealing unique microtubule inner proteins. We further showed that the sperm centrioles and their surrounding matrix form a dynamic basal complex that facilitates a cascade of internal sliding, coupling tail beating with asymmetric head kinking. Although these findings contribute profoundly to the field, the resolution achieved in these studies (~20Å) precluded protein identification in most cases.
Now I plan to develop a workflow based on single particle analysis, achieving near-atomic resolution, but without purification. I will apply this workflow, together with biochemical assays and cellular cryo-electron tomography, to humans and other species to resolve how germ cells get into shape and acquire motility. Specifically, the mechanisms underlining 1) nuclear shaping 2) centriole remodelling 3) mitochondrial sheath assembly 4) motor apparatus activation.
Understanding how male germ cells get into shape is of clinical relevance, as sperm morphological defects are often observed in infertility. Moreover, the success rate of assisted reproduction technologies can be improved with better diagnosis and we expect that the new proteins we identify will help this process. Conversely, understanding the acquisition of motility could potentially be used to develop a male contraceptive.
Status
SIGNEDCall topic
ERC-2022-COGUpdate Date
31-07-2023
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