University of California

Quest Diagnostics Investments, Inc.

Earl Cornell

Raymond C Stevens

Robert A Nordmeyer

Derek T Yegian

Bernard D Santarsiero

Joseph M Jaklevic

Richard E Reitz

Michael P Caulfield

W Henry Benner

Ronald M Krauss

Gloria Kwangja Lee

Patricia J Blanche

Shuguang Li

Peter G Schultz

William F Kolbe

Gyorgy Snell

Thomas N Earnest

Carl W Cork

Jian Jin

Peter G Shultz

Arthur L Jones

Donald C Uber

Joseph M Jaklevich

The invention provides methods of preparation of lipoproteins from a biological sample, including HDL, LDL, Lp(a), IDL, and VLDL, for diagnostic purposes utilizing differential charged particle mobility analysis methods. Further provided are methods for analyzing the size distribution of lipoproteins by differential charged particle mobility, which lipoproteins are prepared by methods of the invention. Further provided are methods for assessing lipid-related health risk, cardiovascular condition, risk of cardiovascular disease, and responsiveness to a therapeutic intervention, which methods utilize lipoprotein size distributions determined by methods of the invention.

Lipoprotein analysis by differential charged-particle mobility

A method and apparatus for the transportation, remote and unattended mounting, and visual alignment and monitoring of protein crystals for synchrotron generated x-ray diffraction analysis. The protein samples are maintained at liquid nitrogen temperatures at all times: during shipment, before mounting, mounting, alignment, data acquisition and following removal. The samples must additionally be stably aligned to within a few microns at a point in space. The ability to accurately perform these tasks remotely and automatically leads to a significant increase in sample throughput and reliability for high-volume protein characterization efforts. Since the protein samples are placed in a shipping-compatible layered stack of sample cassettes each holding many samples, a large number of samples can be shipped in a single cryogenic shipping container.

Integrated crystal mounting and alignment system for high-throughput biological crystallography

A method is provided for performing array microcrystallizations to determine suitable crystallization conditions for a molecule, the method comprising: forming an array of microcrystallizations, each microcrystallization comprising a drop comprising a mother liquor solution whose composition varies within the array and a molecule to be crystallized, the drop having a volume of less than 1 microliter; storing the array of microcrystallizations under conditions suitable for molecule crystals to form in the drops in the array; and detecting molecule crystal formation in the drops by taking images of the drops.

Automated method for setting up multiple crystallization experiments in submicroliter volumes

A method is provided for forming crystallization experiments for a molecule, the method comprising forming a plurality of crystallization experiments that comprise a molecule to be crystallized and a composition that varies among the plurality of crystallization experiments, the crystallization experiments having a volume less than 1 microliter, the volumes of the plurality of crystallization experiments varying among the experiments by less than 25 nL.

Method for performing submicroliter crystallization experiments with high experiment to experiment precision

Method for performing high density submicroliter crystallization experiments

A method is provided for performing crystallization experiments for a molecule, the method comprising performing a plurality of crystallization experiments where the crystallization experiments have volumes of less than 1 microliter, the crystallization experiments comprising a molecule to be crystallized and a composition that varies among the plurality of crystallization experiments detecting crystal formation in the crystallization experiments.

Method for performing submicroliter crystallization experiments

A method is provided for characterizing a crystal structure of a molecule, the method comprising performing a plurality of crystallization experiments where the crystallization experiments have volumes of less than 1 microliter, the crystallization experiments comprising a molecule to be crystallized and a composition that varies among the plurality of crystallization experiments and diffracting a crystal formed in one of the crystallization experiments.

Method for diffracting crystals formed by submicroliter crystallization experiments

Method for screening microcrystallizations for crystal formation

Growing community of inventors

Antioch, CA, United States of America

Earl Cornell