Engineered nanoparticles enable deep proteomics studies at scale by leveraging tunable nano–bio interactions

Author:

Ferdosi Shadi1ORCID,Tangeysh Behzad1,Brown Tristan R.1ORCID,Everley Patrick A.1,Figa Michael1,McLean Matthew1,Elgierari Eltaher M.1,Zhao Xiaoyan1ORCID,Garcia Veder J.1ORCID,Wang Tianyu1,Chang Matthew E. K.2ORCID,Riedesel Kateryna1,Chu Jessica1,Mahoney Max1,Xia Hongwei1,O’Brien Evan S.1,Stolarczyk Craig1,Harris Damian1ORCID,Platt Theodore L.1,Ma Philip1,Goldberg Martin1,Langer Robert3ORCID,Flory Mark R.2,Benz Ryan1,Tao Wei45ORCID,Cuevas Juan Cruz1,Batzoglou Serafim1,Blume John E.1ORCID,Siddiqui Asim1,Hornburg Daniel1,Farokhzad Omid C.145ORCID

Affiliation:

1. Seer, Inc., Redwood City, CA 94065

2. CEDAR Center, Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239-3098

3. David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139

4. Center for Nanomedicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115

5. Department of Anesthesiology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115

Abstract

Significance Deep profiling of the plasma proteome at scale has been a challenge for traditional approaches. We achieve superior performance across the dimensions of precision, depth, and throughput using a panel of surface-functionalized superparamagnetic nanoparticles in comparison to conventional workflows for deep proteomics interrogation. Our automated workflow leverages competitive nanoparticle–protein binding equilibria that quantitatively compress the large dynamic range of proteomes to an accessible scale. Using machine learning, we dissect the contribution of individual physicochemical properties of nanoparticles to the composition of protein coronas. Our results suggest that nanoparticle functionalization can be tailored to protein sets. This work demonstrates the feasibility of deep, precise, unbiased plasma proteomics at a scale compatible with large-scale genomics enabling multiomic studies.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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