SUPPORT AND DEVELOPMENT OF EMAN FOR ELECTRON MICROSCOPY IMAGE PROCESSING

Information

  • Research Project
  • 10242780
  • ApplicationId
    10242780
  • Core Project Number
    R01GM080139
  • Full Project Number
    5R01GM080139-16
  • Serial Number
    080139
  • FOA Number
    PA-19-056
  • Sub Project Id
  • Project Start Date
    6/1/2006 - 17 years ago
  • Project End Date
    8/31/2023 - 8 months ago
  • Program Officer Name
    FLICKER, PAULA F
  • Budget Start Date
    9/1/2021 - 2 years ago
  • Budget End Date
    8/31/2022 - a year ago
  • Fiscal Year
    2021
  • Support Year
    16
  • Suffix
  • Award Notice Date
    9/16/2021 - 2 years ago

SUPPORT AND DEVELOPMENT OF EMAN FOR ELECTRON MICROSCOPY IMAGE PROCESSING

EMAN is one of the most well-established and widely used scientific image processing suites targeting the rapidly growing CryoEM/CryoET community worldwide. In turn, the CryoEM and CryoET studies which it enables permit determination of the structures of interacting macromolecules both in-vitro and in-vivo, and are being used to better understand the biochemical processes taking place in cells, to better identify potential drug targets and develop novel diagnostics. With the higher resolutions now possible in this field, direct drug interaction structural studies are now possible, and being used to gain insight into the mode of action of drugs within the cell. Unlike many newer tools in the field, such as Relion, CisTEM and CryoSparc, which focus on specific refinement tasks, EMAN is a versatile, modular suite capable of performing a variety of image processing tasks with hundreds of algorithms supporting virtually all of the standard file formats and mathematical conventions used in the field, as well as other related imaging fields. It provides an ideal platform for prototyping fundamental new algorithm developments, while still able to achieve data-limited resolution in single particle reconstruction. While high resolution single particle refinement has become routine in recent years, thanks largely to the dramatic data quality improvements provided by new detector technology, there remain significant opportunities for improvements in mitigating model bias, efficient use of data, and analysis of complexes with compositional or conformational variability. Some of the most important problems from a biological perspective involve the sort of compositional and conformational variability which remain challenging problems. The field also remains susceptible to problems of initial model bias, which are exacerbated in systems exhibiting structural variability, and as a result many structures are still published with exaggerated resolution claims. The standard protocols used by many in the field typically involve discarding a very large fraction of the raw data (as much as 80-90% in some cases), often based on qualitative assessments, raising questions related to rigor and reproducibility of structural results. In this proposal, we will develop or adapt image processing techniques to help resolve these issues, based on developments or unrealized concepts from mathematics and computer science.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R01
  • Administering IC
    GM
  • Application Type
    5
  • Direct Cost Amount
    215539
  • Indirect Cost Amount
    129323
  • Total Cost
    344862
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF MEDICINE
  • Funding ICs
    NIGMS:344862\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    MSFD
  • Study Section Name
    Macromolecular Structure and Function D Study Section
  • Organization Name
    BAYLOR COLLEGE OF MEDICINE
  • Organization Department
    BIOCHEMISTRY
  • Organization DUNS
    051113330
  • Organization City
    HOUSTON
  • Organization State
    TX
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    770303411
  • Organization District
    UNITED STATES