Probing Proteoform Heterogeneity from Single Human Oocytes

MS) detection, we identified 559 proteins and 769 unique proteoforms across 28 oocytes from 8 donors, with an average of 78 unique proteoforms per oocyte. We used scPiMS to selectively sample oocytes and cumulus granulosa cells from single cumulus oocyte complexes (COCs) to identify proteoforms specific to these cell types. Finally, we determined proteoform landscapes for members of the oocyte-specific subcortical maternal complex (SCMC), KHDC3 and OOEP, and found new proteoforms that differ with donor age. Together, these first-in-class observations provide a foundation for understanding protein-level changes in oocyte biology across puberty to ultimately improve the efficiency of IVM and make fertility restoration options accessible for more patients.

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Journal
Molecular & Cellular Proteomics
Published
2026-04-01
DOI
https://doi.org/10.1016/j.mcpro.2026.101566
Primary Topic
Reproductive Biology and Fertility
Type
article
Field-Weighted Citation Impact
0.00

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article

Probing Proteoform Heterogeneity from Single Human Oocytes

Kanchustambham Vijayalakshmi, Chelsea Lock, Elizabeth Tsui, Indira Plá et al.
Molecular & Cellular Proteomics
Reproductive Biology and Fertility
article

Probing Proteoform Heterogeneity from Single Human Oocytes

Kanchustambham Vijayalakshmi, Chelsea Lock, Elizabeth Tsui, Indira Plá, Tian Xu, Hannah B. McDowell, Diane C. Saunders, Monica M. Laronda, Neil L. Kelleher, Jared O. Kafader, Nickolas P. Fisher
article en

Abstract

MS) detection, we identified 559 proteins and 769 unique proteoforms across 28 oocytes from 8 donors, with an average of 78 unique proteoforms per oocyte. We used scPiMS to selectively sample oocytes and cumulus granulosa cells from single cumulus oocyte complexes (COCs) to identify proteoforms specific to these cell types. Finally, we determined proteoform landscapes for members of the oocyte-specific subcortical maternal complex (SCMC), KHDC3 and OOEP, and found new proteoforms that differ with donor age. Together, these first-in-class observations provide a foundation for understanding protein-level changes in oocyte biology across puberty to ultimately improve the efficiency of IVM and make fertility restoration options accessible for more patients.

Molecular & Cellular Proteomics
Northwestern University (US), Lurie Children's Hospital (US), Robert H. Lurie Comprehensive Cancer Center of Northwestern University
National Institutes of Health, NIH Office of the Director
Zero hunger
Openalex Percentile: Top 23%
Reproductive Biology and Fertility
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Probing Proteoform Heterogeneity from Single Human Oocytes — Kanchustambham Vijayalakshmi, Chelsea Lock, et al. · Molecular & Cellular Proteomics (2026) | TGRS Research Map | TGRS