Marjan Hadian-Jazi

Dr. Marjan Hadian-Jazi

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Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 September 2025 in Nature Immunology
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CTCarlson Tsui
Carlson Tsui
LHLeonie Heyden
Leonie Heyden
LWLifen Wen
Lifen Wen
CGCatarina Gago da Graça
Catarina Gago da Graça
NPNikita Potemkin
Nikita Potemkin
AKAxel Kallies
Axel Kallies

13 September 2021 in Journal of Applied Crystallography
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Journal Article
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MHMarjan Hadian-Jazi
Marjan Hadian-Jazi
ASAlireza Sadri
Alireza Sadri
ABAnton Barty
Anton Barty
OYOleksandr M. Yefanov
Oleksandr M. Yefanov
MGMarina Galchenkova
Marina Galchenkova
BABrian Abbey
Brian Abbey
A peak-finding algorithm for serial crystallography (SX) data analysis based on the principle of `robust statistics' has been developed. Methods which are statistically robust are generally more insensitive to any departures from model assumptions and are particularly effective when analysing mixtures of probability distributions. For example, these methods enable the discretization of data into a group comprising inliers (i.e. the background noise) and another group comprising outliers (i.e. Bragg peaks). Our robust statistics algorithm has two key advantages, which are demonstrated through testing using multiple SX data sets. First, it is relatively insensitive to the exact value of the input parameters and hence requires minimal optimization. This is critical for the algorithm to be able to run unsupervised, allowing for automated selection or `vetoing' of SX diffraction data. Secondly, the processing of individual diffraction patterns can be easily parallelized. This means that it can analyse data from multiple detector modules simultaneously, making it ideally suited to real-time data processing. These characteristics mean that the robust peak finder (RPF) algorithm will be particularly beneficial for the new class of MHz X-ray free-electron laser sources, which generate large amounts of data in a short period of time.

1 August 2019 in Review of Scientific Instruments
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PBP. Berntsen
P. Berntsen
MHMarjan Hadian-Jazi
Marjan Hadian-Jazi
MKM. Kusel
M. Kusel
Andrew V. MartinAndrew V. Martin
Andrew V. Martin
TET. Ericsson
T. Ericsson
BABrian Abbey
Brian Abbey
A serial millisecond crystallography (SMX) facility has recently been implemented at the macromolecular crystallography beamline, MX2 at the Australian Synchrotron. The setup utilizes a combination of an EIGER X 16M detector system and an in-house developed high-viscosity injector, “Lipidico.” Lipidico uses a syringe needle to extrude the microcrystal-containing viscous media and it is compatible with commercially available syringes. The combination of sample delivery via protein crystals suspended in a viscous mixture and a millisecond frame rate detector enables high-throughput serial crystallography at the Australian Synchrotron. A hit-finding algorithm, based on the principles of “robust-statistics,” is employed to rapidly process the data. Here we present the first SMX experimental results with a detector frame rate of 100 Hz (10 ms exposures) and the Lipidico injector using a mixture of lysozyme microcrystals embedded in high vacuum silicon grease. Details of the experimental setup, sample injector, and data analysis pipeline are designed and developed as part of the Australian Synchrotron SMX instrument and are reviewed here.

3 November 2017 in Journal of Applied Crystallography
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MHMarjan Hadian-Jazi
Marjan Hadian-Jazi
Marc MesserschmidtMarc Messerschmidt
Marc Messerschmidt
Connie DarmaninConnie Darmanin
Connie Darmanin
KGKlaus Giewekemeyer
Klaus Giewekemeyer
AMAdrian P. Mancuso
Adrian P. Mancuso
BABrian Abbey
Brian Abbey

21 March 2022 in Journal of Synchrotron Radiation
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DWDaniel J. Wells
Daniel J. Wells
PBPeter Berntsen
Peter Berntsen
EBEugeniu Balaur
Eugeniu Balaur
CKCameron Kewish
Cameron Kewish
PAPatrick Adams
Patrick Adams
Connie DarmaninConnie Darmanin
Connie Darmanin
Serial crystallography of membrane proteins often employs high-viscosity injectors (HVIs) to deliver micrometre-sized crystals to the X-ray beam. Typically, the carrier medium is a lipidic cubic phase (LCP) media, which can also be used to nucleate and grow the crystals. However, despite the fact that the LCP is widely used with HVIs, the potential impact of the injection process on the LCP structure has not been reported and hence is not yet well understood. The self-assembled structure of the LCP can be affected by pressure, dehydration and temperature changes, all of which occur during continuous flow injection. These changes to the LCP structure may in turn impact the results of X-ray diffraction measurements from membrane protein crystals. To investigate the influence of HVIs on the structure of the LCP we conducted a study of the phase changes in monoolein/water and monoolein/buffer mixtures during continuous flow injection, at both atmospheric pressure and under vacuum. The reservoir pressure in the HVI was tracked to determine if there is any correlation with the phase behaviour of the LCP. The results indicated that, even though the reservoir pressure underwent (at times) significant variation, this did not appear to correlate with observed phase changes in the sample stream or correspond to shifts in the LCP lattice parameter. During vacuum injection, there was a three-way coexistence of the gyroid cubic phase, diamond cubic phase and lamellar phase. During injection at atmospheric pressure, the coexistence of a cubic phase and lamellar phase in the monoolein/water mixtures was also observed. The degree to which the lamellar phase is formed was found to be strongly dependent on the co-flowing gas conditions used to stabilize the LCP stream. A combination of laboratory-based optical polarization microscopy and simulation studies was used to investigate these observations.

9 January 2021 in Crystals
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MHMarjan Hadian-Jazi
Marjan Hadian-Jazi
PBPeter Berntsen
Peter Berntsen
HMHugh Marman
Hugh Marman
BABrian Abbey
Brian Abbey
Connie DarmaninConnie Darmanin
Connie Darmanin
Serial Synchrotron Crystallography (SSX) is rapidly emerging as a promising technique for collecting data for time-resolved structural studies or for performing room temperature micro-crystallography measurements using micro-focused beamlines. SSX is often performed using high frame rate detectors in combination with continuous sample scanning or high-viscosity or liquid jet injectors. When performed using ultra-bright X-ray Free Electron Laser (XFEL) sources serial crystallography typically involves a process known as ’diffract-and-destroy’ where each crystal is measured just once before it is destroyed by the intense XFEL pulse. In SSX, however, particularly when using high-viscosity injectors (HVIs) such as Lipidico, the crystal can be intercepted multiple times by the X-ray beam prior to exiting the interaction region. This has a number of important consequences for SSX including whether these multiple-hits can be incorporated into the data analysis or whether they need to be excluded due to the potential impact of radiation damage. Here, we investigate the occurrence and characteristics of multiple hits on single crystals using SSX with lipidico. SSX data are collected from crystals as they tumble within a high viscous stream of silicone grease flowing through a micro-focused X-ray beam. We confirmed that, using the Eiger 16M, we are able to collect up to 42 frames of data from the same single crystal prior to it leaving the X-ray interaction region. The frequency and occurrence of multiple hits may be controlled by varying the sample flow rate and X-ray beam size. Calculations of the absorbed dose confirm that these crystals are likely to undergo radiation damage but that nonetheless incorporating multiple hits into damage-free data should lead to a significant reduction in the number of crystals required for structural analysis when compared to just looking at a single diffraction pattern from each crystal.